Maltose (BioDeep_00000014323)

 

Secondary id: BioDeep_00000014974

natural product human metabolite PANOMIX_OTCML-2023 Endogenous blood metabolite BioNovoGene_Lab2019


代谢物信息卡片


(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-{[(2R,3S,4R,5S,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}oxane-3,4,5-triol

化学式: C12H22O11 (342.1162)
中文名称: D-(+)-麦芽糖, D-(+)-麦芽糖一水合物, 麦芽糖浆, D-麦芽糖
谱图信息: 最多检出来源 Homo sapiens(plant) 33.58%

Reviewed

Last reviewed on 2024-09-14.

Cite this Page

Maltose. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China. https://query.biodeep.cn/s/maltose (retrieved 2024-12-26) (BioDeep RN: BioDeep_00000014323). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

分子结构信息

SMILES: C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O
InChI: InChI=1/C12H22O11/c13-1-3-5(15)6(16)9(19)12(22-3)23-10-4(2-14)21-11(20)8(18)7(10)17/h3-20H,1-2H2/t3-,4-,5-,6+,7-,8-,9-,10-,11?,12-/m1/s1

描述信息

D-Maltose, also known as maltose, maltobiose or malt sugar, is a disaccharide formed from two units of glucose joined with an alpha (1→4) bond. Its name comes from malt, combined with the suffix -ose which is used in names of sugars. Maltose is a key structural motif of starch. When alpha-amylase breaks down starch, it removes two glucose units at a time, producing maltose. Maltose can be further broken down to glucose by the maltase enzyme, which catalyses the hydrolysis of the glycosidic bond. D-maltose exists in all living species, ranging from bacteria to plants to humans. Within humans, D-maltose participates in a number of enzymatic reactions. In particular, maltose can be converted into glucose; which is mediated by the enzyme maltase-glucoamylase. In addition, maltose can be converted into glucose through its interaction with the enzyme glycogen debranching enzyme. Maltose is found in high concentrations in oriental wheats and in a lower concentrations in sweet potato, grape wines, yellow pond-lilies, sunflowers, and spinach. Maltose is a component of malt, a substance which is obtained in the process of allowing grain to soften in water and germinate. It is also present in highly variable quantities in partially hydrolysed starch products like maltodextrin, corn syrup and acid-thinned starch. Maltose has a sweet taste but is only about 30–60\\\\% as sweet as sucrose, depending on the concentration.
Sweetening agent, dietary supplement. Occurs in some plants as hydrolytic dec. production of starch. Production in high yield (80\\\\%) by the action of diastase (a- and b-amylase) on starch, a process used in brewing
D000074385 - Food Ingredients > D005503 - Food Additives
D010592 - Pharmaceutic Aids > D005421 - Flavoring Agents
Maltose is a disaccharide formed from two units of glucose joined with an α(1→4) bond, a reducing sugar. Maltose monohydrate can be used as a energy source for bacteria.
Maltose is a disaccharide formed from two units of glucose joined with an α(1→4) bond, a reducing sugar. Maltose monohydrate can be used as a energy source for bacteria.

同义名列表

46 个代谢物同义名

(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-{[(2R,3S,4R,5S,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}oxane-3,4,5-triol; 1-alpha-delta-Glucopyranosyl-4-alpha-delta-glucopyranose; alpha-delta-Glucopyranosyl-(1->4)-delta-glucopyranose; 4-(alpha-delta-Glucopyranosido)-alpha-glucopyranose; 4-O-alpha-delta-Glucopyranosyl-delta-glucopyranose; 4-O-alpha-D-Glucopyranosyl-alpha-D-mannopyranose; 1-alpha-D-Glucopyranosyl-4-alpha-D-glucopyranose; alpha-delta-Glucopyranosyl-(1->4)-delta-glucose; 4-(alpha-D-Glucopyranosido)-alpha-glucopyranose; alpha-D-Glucopyranosyl-(1->4)-D-glucopyranose; 4-O-alpha-delta-Glucopyranosyl-delta-glucose; 4-O-alpha-D-Glucopyranosyl-D-glucopyranose; 4-O-a-D-Glucopyranosyl-a-D-mannopyranose; 4-O-Α-D-glucopyranosyl-α-D-mannopyranose; 4-(alpha-delta-Glucosido)-delta-glucose; alpha-D-Glucopyranosyl-(1->4)-D-glucose; 4-O-alpha-D-Glucopyranosyl-D-glucose; alpha-delta-GLCP-(1->4)-delta-GLCP; 4-O-a-D-Glucopyranosyl-D-glucose; 4-(alpha-D-Glucosido)-D-glucose; alpha-D-GLCP-(1->4)-D-GLCP; delta-(+)-Maltose; alpha-Malt sugar; Maltose solution; D-(+)-Maltose; Cextromaltose; delta-Maltose; Advantose 100; Maltose HHH; Maltose HH; Finetose F; Maltodiose; Malt sugar; Malzzucker; Maltobiose; D-Maltose; Martos-10; Sunmalt S; Finetose; Sunmalt; Madoros; Maltose; Maltos; D-Maltose; L-Glc(a1-4)a-L-Glc; Maltose



数据库引用编号

26 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(9)

BioCyc(8)

PlantCyc(3)

代谢反应

26 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(1)

COVID-19 Disease Map(0)

PathBank(25)

PharmGKB(0)

72 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有：

  • PubMed: 来源于PubMed文献库中的文献信息，我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表，这个列表按照代谢物同时出现的文献数量降序排序，取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘，得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序，取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中，存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称，可以跳转到相关代谢物的信息页面。

亚细胞结构定位 关联基因列表
Cytoplasm 6 ALB, APC, G6PD, GCK, HPGDS, TXN
Peripheral membrane protein 4 G6PD, GBA1, GCK, HSD17B6
Endoplasmic reticulum membrane 1 CD4
Nucleus 4 ALB, APC, GCK, TXN
cytosol 8 AGXT, ALB, APC, G6PD, GCK, HPGDS, LIPE, TXN
trans-Golgi network 1 GBA1
centrosome 2 ALB, APC
nucleoplasm 5 APC, ATP2B1, GCK, HPGDS, TXN
Cell membrane 5 APC, ATP2B1, CD4, LIPE, TREH
lamellipodium 1 APC
ruffle membrane 1 APC
Early endosome membrane 1 HSD17B6
Multi-pass membrane protein 2 ATP2B1, MAL2
Golgi apparatus membrane 1 GCK
Synapse 1 ATP2B1
glutamatergic synapse 2 ATP2B1, MAL2
Golgi apparatus 4 ALB, APC, GBA1, SI
Golgi membrane 2 GCK, INS
lysosomal membrane 1 GBA1
presynaptic membrane 1 ATP2B1
Cytoplasm, cytosol 2 G6PD, LIPE
Lysosome 1 GBA1
plasma membrane 6 APC, ATP2B1, CD4, LCT, SI, TREH
synaptic vesicle membrane 2 ATP2B1, MAL2
Membrane 6 ATP2B1, G6PD, LIPE, MAL2, SI, TREH
apical plasma membrane 2 MAL2, SI
basolateral plasma membrane 2 ATP2B1, GCK
brush border 1 SI
caveola 1 LIPE
extracellular exosome 10 ALB, AMY2A, ATP2B1, G6PD, GBA1, LYZ, MAL2, SI, TREH, TXN
Lysosome membrane 1 GBA1
Lumenal side 2 GBA1, HSD17B6
endoplasmic reticulum 4 ALB, GBA1, H6PD, HSD17B6
extracellular space 4 ALB, AMY2A, INS, LYZ
lysosomal lumen 1 GBA1
perinuclear region of cytoplasm 2 APC, MAL2
adherens junction 1 APC
bicellular tight junction 1 APC
mitochondrion 1 GCK
protein-containing complex 1 ALB
intracellular membrane-bounded organelle 5 AGXT, ATP2B1, G6PD, HPGDS, HSD17B6
Microsome membrane 1 HSD17B6
Single-pass type I membrane protein 2 CD4, LCT
Secreted 3 ALB, INS, TXN
extracellular region 5 ALB, AMY2A, INS, LYZ, TXN
cytoplasmic side of plasma membrane 1 G6PD
hippocampal mossy fiber to CA3 synapse 1 MAL2
anchoring junction 1 ALB
centriolar satellite 1 G6PD
Cytoplasmic vesicle, secretory vesicle, synaptic vesicle membrane 1 ATP2B1
external side of plasma membrane 1 CD4
beta-catenin destruction complex 1 APC
Wnt signalosome 1 APC
Early endosome 1 CD4
Apical cell membrane 1 LCT
Cell projection, lamellipodium 1 APC
Cell projection, ruffle membrane 1 APC
Membrane raft 2 CD4, MAL2
Cytoplasm, cytoskeleton 1 APC
microtubule 1 APC
Cell junction, adherens junction 1 APC
Peroxisome 1 AGXT
peroxisomal matrix 1 AGXT
lateral plasma membrane 2 APC, ATP2B1
ciliary basal body 1 ALB
cell projection 1 ATP2B1
cell periphery 1 APC
centriole 1 ALB
spindle pole 1 ALB
blood microparticle 1 ALB
Basolateral cell membrane 2 ATP2B1, GCK
Lipid-anchor, GPI-anchor 1 TREH
endosome lumen 1 INS
Lipid droplet 1 LIPE
Membrane, caveola 1 LIPE
Presynaptic cell membrane 1 ATP2B1
side of membrane 1 TREH
secretory granule lumen 1 INS
Golgi lumen 1 INS
endoplasmic reticulum lumen 4 ALB, CD4, H6PD, INS
platelet alpha granule lumen 1 ALB
specific granule lumen 1 LYZ
tertiary granule lumen 1 LYZ
kinetochore 1 APC
transport vesicle 1 INS
azurophil granule lumen 1 LYZ
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
immunological synapse 1 ATP2B1
clathrin-coated endocytic vesicle membrane 1 CD4
external side of apical plasma membrane 1 LCT
catenin complex 1 APC
T cell receptor complex 1 CD4
photoreceptor ribbon synapse 1 ATP2B1
ciliary transition fiber 1 ALB


文献列表

  • Xinyue Zhai, Xinwei Tao, Yuqian Wu, Kesun Jin, Huaping Tan, Tianle Zhou, Yong Chen. Injectable and Self-Adaptive Gel Scaffold Based on Heparin Microspheres for Adipogenesis of Human Adipose-Derived Stem Cells. Biomacromolecules. 2023 Sep; ?(?):. doi: 10.1021/acs.biomac.3c00348. [PMID: 37722066]
  • Yuang Wu, Yue Sun, Evelyne Richet, Zhifu Han, Jijie Chai. Structural basis for negative regulation of the Escherichia coli maltose system. Nature communications. 2023 08; 14(1):4925. doi: 10.1038/s41467-023-40447-y. [PMID: 37582800]
  • Patricia Benito, Javier Bellón, Rosa Porcel, Lynne Yenush, José M Mulet. The Biostimulant, Potassium Humate Ameliorates Abiotic Stress in Arabidopsis thaliana by Increasing Starch Availability. International journal of molecular sciences. 2023 Jul; 24(15):. doi: 10.3390/ijms241512140. [PMID: 37569516]
  • Ayako Wada-Katsumata, Eduardo Hatano, Coby Schal. Gustatory polymorphism mediates a new adaptive courtship strategy. Proceedings. Biological sciences. 2023 03; 290(1995):20222337. doi: 10.1098/rspb.2022.2337. [PMID: 36987637]
  • Samantha McPherson, Ayako Wada-Katsumata, Jules Silverman, Coby Schal. Glucose- and disaccharide-containing baits impede secondary mortality in glucose-averse German cockroaches. Journal of economic entomology. 2023 Mar; ?(?):. doi: 10.1093/jee/toad030. [PMID: 36888567]
  • Liangke Chen, Xiangbai Dong, Huifang Yang, Yaru Chai, Yan Xia, Lihong Tian, Le Qing Qu. Cytosolic disproportionating enzyme2 is essential for pollen germination and pollen tube elongation in rice. Plant physiology. 2023 01; 191(1):96-109. doi: 10.1093/plphys/kiac496. [PMID: 36282529]
  • Tengfei Liu, Md Abu Kawochar, Shengxuan Liu, Yunxia Cheng, Shahnewaz Begum, Enshuang Wang, Tingting Zhou, Tiantian Liu, Xingkui Cai, Botao Song. Suppression of the tonoplast sugar transporter, StTST3.1, affects transitory starch turnover and plant growth in potato. The Plant journal : for cell and molecular biology. 2023 01; 113(2):342-356. doi: 10.1111/tpj.16050. [PMID: 36444716]
  • Mikel Redin Hurtado, Ida Fischer, Matthias Laska. Is sugar as sweet to the palate as seeds are appetizing to the belly? Taste responsiveness to five food-associated carbohydrates in zoo-housed white-faced sakis, Pithecia pithecia. PloS one. 2023; 18(10):e0292175. doi: 10.1371/journal.pone.0292175. [PMID: 37906563]
  • A Ruiz-Gayosso, I Rodríguez-Cruz, E Martínez-Barajas, P Coello. Phosphorylation of DPE2 at S786 partially regulates starch degradation. Plant physiology and biochemistry : PPB. 2022 Dec; 193(?):70-77. doi: 10.1016/j.plaphy.2022.10.024. [PMID: 36335878]
  • Avinash Kumar, Vinay Kumar Singh, Arvind M Kayastha. Molecular modeling, docking and dynamics studies of fenugreek (Trigonella foenum-graecum) α-amylase. Journal of biomolecular structure & dynamics. 2022 Nov; ?(?):1-16. doi: 10.1080/07391102.2022.2144458. [PMID: 36369783]
  • Lianyu Zhou, Lu Jiao, Jiasheng Ju, Xuelan Ma. Effect of Sodium Selenite on the Metabolite Profile of Epichloë sp. Mycelia from Festuca sinensis in Solid Culture. Biological trace element research. 2022 Nov; 200(11):4865-4879. doi: 10.1007/s12011-021-03054-w. [PMID: 34973128]
  • Michail Michailidis, Vaia Styliani Titeli, Evangelos Karagiannis, Kyriaki Feidaki, Ioannis Ganopoulos, Georgia Tanou, Anagnostis Argiriou, Athanassios Molassiotis. Tissue-specific transcriptional analysis outlines calcium-induced core metabolic changes in sweet cherry fruit. Plant physiology and biochemistry : PPB. 2022 Oct; 189(?):139-152. doi: 10.1016/j.plaphy.2022.08.022. [PMID: 36087439]
  • Yijun Liu, Yuhan Zeng, Yixin Liu, Xiaoya Wang, Yuhuan Chen, Dion Lepp, Rong Tsao, Tsuyoshi Sadakiyo, Hua Zhang, Yoshinori Mine. Regulatory Effect of Isomaltodextrin on a High-Fat Diet Mouse Model with LPS-Induced Low-Grade Chronic Inflammation. Journal of agricultural and food chemistry. 2022 Sep; 70(36):11258-11273. doi: 10.1021/acs.jafc.2c03391. [PMID: 36041062]
  • Yangyang Geng, Shixin Zhang, Ningxian Yang, Likang Qin. Whole-Genome Sequencing and Comparative Genomics Analysis of the Wild Edible Mushroom (Gomphus purpuraceus) Provide Insights into Its Potential Food Application and Artificial Domestication. Genes. 2022 09; 13(9):. doi: 10.3390/genes13091628. [PMID: 36140797]
  • Andrea Hoehnel, Jairo Salas García, Christine Coffey, Emanuele Zannini, Elke K Arendt. Comparative study of sugar extraction procedures for HPLC analysis and proposal of an ethanolic extraction method for plant-based high-protein ingredients. Journal of the science of food and agriculture. 2022 Sep; 102(12):5055-5064. doi: 10.1002/jsfa.11204. [PMID: 33709392]
  • Qiubin Huang, Huiping Liu, Juanmei Zhang, Shaowei Wang, Fengying Liu, Chengdie Li, Gang Wang. Production of extracellular amylase contributes to the colonization of Bacillus cereus 0-9 in wheat roots. BMC microbiology. 2022 08; 22(1):205. doi: 10.1186/s12866-022-02618-7. [PMID: 35996113]
  • Javad Hassanzadeh, Haider A J Al Lawati, Nafiseh Bagheri. On paper synthesis of multifunctional CeO2 nanoparticles@Fe-MOF composite as a multi-enzyme cascade platform for multiplex colorimetric detection of glucose, fructose, sucrose, and maltose. Biosensors & bioelectronics. 2022 Jul; 207(?):114184. doi: 10.1016/j.bios.2022.114184. [PMID: 35339073]
  • Yaping Ma, Yaru Han, Xuerui Feng, Handong Gao, Bing Cao, Lihua Song. Genome-wide identification of BAM (β-amylase) gene family in jujube (Ziziphus jujuba Mill.) and expression in response to abiotic stress. BMC genomics. 2022 Jun; 23(1):438. doi: 10.1186/s12864-022-08630-5. [PMID: 35698031]
  • Xiangxiang Kong, Chunxia Li, Xiaodong Sun, Bing Niu, Dehua Guo, Yuan Jiang, Jielin Yang, Qin Chen. The maltose transporter subunit IICB of the phosphotransferase system: An important factor for biofilm formation of Cronobacter. International journal of food microbiology. 2022 Jun; 370(?):109517. doi: 10.1016/j.ijfoodmicro.2021.109517. [PMID: 35216827]
  • Felix Funk, Klaus Weber, Naja Nyffenegger, Jens-Alexander Fuchs, Amy Barton. Tissue biodistribution of intravenous iron-carbohydrate nanomedicines differs between preparations with varying physicochemical characteristics in an anemic rat model. European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V. 2022 May; 174(?):56-76. doi: 10.1016/j.ejpb.2022.03.006. [PMID: 35337966]
  • Sarah Tassinari, Silvia Moreno, Hartmut Komber, Riccardo Carloni, Michela Cangiotti, Maria Francesca Ottaviani, Dietmar Appelhans. Synthesis and biological and physico-chemical characterization of glycodendrimers and oligopeptides for the treatment of systemic lupus erythematosus. Nanoscale. 2022 Mar; 14(12):4654-4670. doi: 10.1039/d1nr06583a. [PMID: 35262128]
  • Beibei Wei, Wei Xia, Lei Wang, Xuewei Jin, Weikang Yang, Deming Rao, Sheng Chen, Jing Wu. Diverse prebiotic effects of isomaltodextrins with different glycosidic linkages and molecular weights on human gut bacteria in vitro. Carbohydrate polymers. 2022 Mar; 279(?):118986. doi: 10.1016/j.carbpol.2021.118986. [PMID: 34980347]
  • Raquel López-Vilella, Silvia Lozano-Edo, Patricia Arenas Martín, Pablo Jover-Pastor, Meryem Ezzitouny, José Sorolla Romero, María Calvo Asensio, Julia Martínez-Solé, Borja Guerrero Cervera, José Carlos Sánchez Martínez, Víctor Donoso Trenado, Ignacio Sánchez-Lázaro, Luis Martinez Dolz, Luis Almenar Bonet. Impact of intravenous ferric carboxymaltose on heart failure with preserved and reduced ejection fraction. ESC heart failure. 2022 02; 9(1):133-145. doi: 10.1002/ehf2.13753. [PMID: 34964300]
  • Tomoya Goto, Tomoki Umeda, Shingo Hino, Tatsuya Morita, Naomichi Nishimura. Oral Intake of Slowly Digestible α-Glucan Such as Resistant Maltodextrin Leads to Increased Secretion of Glucagon-Like Peptide-2 in Rats and Helps Thicken Their Ileal Mucosae. Journal of nutritional science and vitaminology. 2022; 68(2):104-111. doi: 10.3177/jnsv.68.104. [PMID: 35491199]
  • Lourdes M DelRosso, Raffaele Ferri, Maida L Chen, Vidhi Kapoor, Richard P Allen, Maria Paola Mogavero, Daniel L Picchietti. Clinical efficacy and safety of intravenous ferric carboxymaltose treatment of pediatric restless legs syndrome and periodic limb movement disorder. Sleep medicine. 2021 11; 87(?):114-118. doi: 10.1016/j.sleep.2021.08.030. [PMID: 34562823]
  • Orhan Efe, Juan David Cala García, David Bruce Mount, Alice Marie Sheridan. Refractory hypophosphatemia following ferric carboxymaltose administration. CEN case reports. 2021 11; 10(4):473-475. doi: 10.1007/s13730-021-00590-1. [PMID: 33715107]
  • Moupriya Nag, Dibyajit Lahiri, Sayantani Garai, Dipro Mukherjee, Rina Rani Ray. Regulation of β-amylase synthesis: a brief overview. Molecular biology reports. 2021 Sep; 48(9):6503-6511. doi: 10.1007/s11033-021-06613-5. [PMID: 34379288]
  • Amália Ferreira, Thiago Cahú, Jinchuan Xu, Andreas Blennow, Ranilson Bezerra. A highly stable raw starch digesting α-amylase from Nile tilapia (Oreochromis niloticus) viscera. Food chemistry. 2021 Aug; 354(?):129513. doi: 10.1016/j.foodchem.2021.129513. [PMID: 33765464]
  • Sant-Rayn Pasricha, Michael Gilbertson, Tishya Indran, Ashwini Bennett, Matthew van Dam, Elizabeth Coughlin, Anouk Dev, Sanjeev Chunilal, Stephen Opat. Safety of rapid injection of undiluted ferric carboxymaltose to patients with iron-deficiency anaemia: a Phase II single-arm study. Internal medicine journal. 2021 Aug; 51(8):1304-1311. doi: 10.1111/imj.15195. [PMID: 33462917]
  • Tao Tian, Guo-Ying Chen, Hao Zhang, Feng-Qing Yang. Personal Glucose Meter for α-Glucosidase Inhibitor Screening Based on the Hydrolysis of Maltose. Molecules (Basel, Switzerland). 2021 Jul; 26(15):. doi: 10.3390/molecules26154638. [PMID: 34361791]
  • Ewelina Rogozińska, Jahnavi Daru, Marios Nicolaides, Carmen Amezcua-Prieto, Susan Robinson, Rui Wang, Peter J Godolphin, Carlos Martín Saborido, Javier Zamora, Khalid S Khan, Shakila Thangaratinam. Iron preparations for women of reproductive age with iron deficiency anaemia in pregnancy (FRIDA): a systematic review and network meta-analysis. The Lancet. Haematology. 2021 Jul; 8(7):e503-e512. doi: 10.1016/s2352-3026(21)00137-x. [PMID: 34171281]
  • Lucia Cococcioni, Licia Pensabene, Sara El-Khouly, Sibongile Chadokufa, Sara McCartney, Efstratios Saliakellis, Fevronia Kiparissi, Osvaldo Borrelli. Ferric carboxymaltose treatment for iron deficiency anemia in children with inflammatory bowel disease: Efficacy and risk of hypophosphatemia. Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver. 2021 07; 53(7):830-834. doi: 10.1016/j.dld.2021.02.017. [PMID: 33775573]
  • Tina B Schreier, Brendan Fahy, Laure C David, Hamad Siddiqui, Roger Castells-Graells, Alison M Smith. Introduction of glucan synthase into the cytosol in wheat endosperm causes massive maltose accumulation and represses starch synthesis. The Plant journal : for cell and molecular biology. 2021 06; 106(5):1431-1442. doi: 10.1111/tpj.15246. [PMID: 33764607]
  • Hye Won Shin, Doo Yeon Go, Suk Woo Lee, Yoon Ji Choi, Eun Ji Ko, Hae Sun You, Yoo Kyung Jang. Comparative efficacy and safety of intravenous ferric carboxymaltose and iron sucrose for iron deficiency anemia in obstetric and gynecologic patients: A systematic review and meta-analysis. Medicine. 2021 May; 100(20):e24571. doi: 10.1097/md.0000000000024571. [PMID: 34011020]
  • Benedikt Schaefer, Moritz Tobiasch, André Viveiros, Herbert Tilg, Nicholas A Kennedy, Myles Wolf, Heinz Zoller. Hypophosphataemia after treatment of iron deficiency with intravenous ferric carboxymaltose or iron isomaltoside-a systematic review and meta-analysis. British journal of clinical pharmacology. 2021 05; 87(5):2256-2273. doi: 10.1111/bcp.14643. [PMID: 33188534]
  • Kamyar Kalantar-Zadeh, Tomas Ganz, Henry Trumbo, Melvin H Seid, Lawrence T Goodnough, Michael A Levine. Parenteral iron therapy and phosphorus homeostasis: A review. American journal of hematology. 2021 05; 96(5):606-616. doi: 10.1002/ajh.26100. [PMID: 33471363]
  • Luigi Cirillo, Chiara Somma, Marco Allinovi, Alfredo Bagalà, Giuseppe Ferro, Elio Di Marcantonio, Stefania Bellelli, Lorenzo Antonio Dallari, Piercarlo Ballo, Pietro Claudio Dattolo. Ferric carboxymaltose vs. ferrous sulfate for the treatment of anemia in advanced chronic kidney disease: an observational retrospective study and cost analysis. Scientific reports. 2021 04; 11(1):7463. doi: 10.1038/s41598-021-86769-z. [PMID: 33811227]
  • Alexander Dashwood, Cassandra Vale, Shaaheen Laher, Fiona Chui, Karen Hay, Yee Weng Wong. Hypophosphatemia Is Common After Intravenous Ferric Carboxymaltose Infusion Among Patients With Symptomatic Heart Failure With Reduced Ejection Fraction. Journal of clinical pharmacology. 2021 04; 61(4):515-521. doi: 10.1002/jcph.1754. [PMID: 33051909]
  • Apostolos Karavidas, Efstratios Troganis, George Lazaros, Despina Balta, Ioannis-Nektarios Karavidas, Eftihia Polyzogopoulou, John Parissis, Dimitrios Farmakis. Oral sucrosomial iron improves exercise capacity and quality of life in heart failure with reduced ejection fraction and iron deficiency: a non-randomized, open-label, proof-of-concept study. European journal of heart failure. 2021 04; 23(4):593-597. doi: 10.1002/ejhf.2092. [PMID: 33421230]
  • Xin Zhang, Zihan Wang, Ziyuan Liu, Bin Liu, Rufen Wu, Zhengbo Chen, Xia Zuo. New application of a traditional method: colorimetric sensor array for reducing sugars based on the in-situ formation of core-shell gold nanorod-coated silver nanoparticles by the traditional Tollens reaction. Mikrochimica acta. 2021 03; 188(4):142. doi: 10.1007/s00604-021-04796-z. [PMID: 33774720]
  • Moheddine Wehbie, Kenechi Kanayo Onyia, Florian Mahler, Aline Le Roy, Anais Deletraz, Ilham Bouchemal, Carolyn Vargas, Jonathan Oyebamiji Babalola, Cécile Breyton, Christine Ebel, Sandro Keller, Grégory Durand. Maltose-Based Fluorinated Surfactants for Membrane-Protein Extraction and Stabilization. Langmuir : the ACS journal of surfaces and colloids. 2021 02; 37(6):2111-2122. doi: 10.1021/acs.langmuir.0c03214. [PMID: 33539092]
  • Lourdes M DelRosso, Daniel L Picchietti, Raffaele Ferri. Comparison between oral ferrous sulfate and intravenous ferric carboxymaltose in children with restless sleep disorder. Sleep. 2021 02; 44(2):. doi: 10.1093/sleep/zsaa155. [PMID: 32840615]
  • Lorenzo Bertani, Domenico Tricò, Federico Zanzi, Giovanni Baiano Svizzero, Francesca Coppini, Nicola de Bortoli, Massimo Bellini, Luca Antonioli, Corrado Blandizzi, Santino Marchi. Oral Sucrosomial Iron Is as Effective as Intravenous Ferric Carboxy-Maltose in Treating Anemia in Patients with Ulcerative Colitis. Nutrients. 2021 Feb; 13(2):. doi: 10.3390/nu13020608. [PMID: 33673371]
  • Seiko Ito, Eiko Arai. Improvement of gluten-free steamed bread quality by partial substitution of rice flour with powder of Apios americana tuber. Food chemistry. 2021 Feb; 337(?):127977. doi: 10.1016/j.foodchem.2020.127977. [PMID: 32919271]
  • Yaling Lu, Xiangping Wu, Lei Yuan, Yingdi Li, Penghui Wang, Jianna Yu, Pingfang Tian, Wenjie Liu. A rapid liquid chromatography-electrospray ionization-ion mobility spectrometry method for monitoring nine representative metabolites in the seedlings of cucumber and wheat. Journal of separation science. 2021 Feb; 44(3):709-716. doi: 10.1002/jssc.202000811. [PMID: 33245598]
  • Adonice Khoury, Kaley A Pagan, Michelle Z Farland. Ferric Maltol: A New Oral Iron Formulation for the Treatment of Iron Deficiency in Adults. The Annals of pharmacotherapy. 2021 02; 55(2):222-229. doi: 10.1177/1060028020941014. [PMID: 32633548]
  • Piotr Ponikowski, Bridget-Anne Kirwan, Stefan D Anker, Theresa McDonagh, Maria Dorobantu, Jarosław Drozdz, Vincent Fabien, Gerasimos Filippatos, Udo Michael Göhring, Andre Keren, Irakli Khintibidze, Hans Kragten, Felipe A Martinez, Marco Metra, Davor Milicic, José C Nicolau, Marcus Ohlsson, Alexander Parkhomenko, Domingo A Pascual-Figal, Frank Ruschitzka, David Sim, Hadi Skouri, Peter van der Meer, Basil S Lewis, Josep Comin-Colet, Stephan von Haehling, Alain Cohen-Solal, Nicolas Danchin, Wolfram Doehner, Henry J Dargie, Michael Motro, Javed Butler, Tim Friede, Klaus H Jensen, Stuart Pocock, Ewa A Jankowska. Ferric carboxymaltose for iron deficiency at discharge after acute heart failure: a multicentre, double-blind, randomised, controlled trial. Lancet (London, England). 2020 12; 396(10266):1895-1904. doi: 10.1016/s0140-6736(20)32339-4. [PMID: 33197395]
  • Wendy Schijns, Abel Boerboom, Margot de Bruyn Kops, Christel de Raaff, Bart van Wagensveld, Frits J Berends, Ignace M C Janssen, Cees J H M van Laarhoven, Hans de Boer, Edo O Aarts. A randomized controlled trial comparing oral and intravenous iron supplementation after Roux-en-Y gastric bypass surgery. Clinical nutrition (Edinburgh, Scotland). 2020 12; 39(12):3779-3785. doi: 10.1016/j.clnu.2020.04.010. [PMID: 32402684]
  • Laura Gobbi, Giuseppe Scaparrotta, Matteo Rigato, Leda Cattarin, Laila Qassim, Gianni Carraro, Barbara Rossi, Lorenzo A Calò. Intravenous ferric carboxymaltose for iron deficiency anemia in dialysis patients: Effect of a new protocol adopted for a hemodialysis limited assistance center. Therapeutic apheresis and dialysis : official peer-reviewed journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy. 2020 Dec; 24(6):642-647. doi: 10.1111/1744-9987.13488. [PMID: 32154642]
  • Rebecca Frazier, Alexander Hodakowski, Xuan Cai, Jungwha Lee, Anaadriana Zakarija, Brady Stein, Valentin David, Myles Wolf, Tamara Isakova, Rupal Mehta. Effects of ferric carboxymaltose on markers of mineral and bone metabolism: A single-center prospective observational study of women with iron deficiency. Bone. 2020 12; 141(?):115559. doi: 10.1016/j.bone.2020.115559. [PMID: 32730929]
  • Eun Yeong Jang, Ki-Bae Hong, Yeok Boo Chang, Jungcheul Shin, Eun Young Jung, Kyungae Jo, Hyung Joo Suh. In Vitro Prebiotic Effects of Malto-Oligosaccharides Containing Water-Soluble Dietary Fiber. Molecules (Basel, Switzerland). 2020 Nov; 25(21):. doi: 10.3390/molecules25215201. [PMID: 33182247]
  • Shashi Kant, Partha Haldar, Sumit Malhotra, Ravneet Kaur, Ramashankar Rath, Olivia Marie Jacob. Intravenous ferric carboxymaltose rapidly increases haemoglobin and serum ferritin among pregnant females with moderate-to-severe anaemia: A single-arm, open-label trial. The National medical journal of India. 2020 Nov; 33(6):324-328. doi: 10.4103/0970-258x.321145. [PMID: 34341207]
  • Hea Ree Park, Su Jung Choi, Eun Yeon Joo, Richard P Allen. Patient characteristics predicting responses to intravenous ferric carboxymaltose treatment of restless legs syndrome. Sleep medicine. 2020 11; 75(?):81-87. doi: 10.1016/j.sleep.2020.02.027. [PMID: 32853922]
  • Javier Jacob, Òscar Miró, Carles Ferre, Carmen Borraz-Ordás, Guillermo Llopis-García, Rosa Comabella, José María Fernández-Cañadas, Amparo Mercado, Alex Roset, Fernando Richard-Espiga, Amparo Valero-Domènech, José Luis Martínez-Gimeno, Francisco Javier Martín-Sánchez, Pere Llorens, Pablo Berrocal-Gil, María José Pérez-Durá, José María Álvarez-Pérez, Pilar López-Díez, Pablo Herrero-Puente, Josep Comín-Colet. Iron deficiency and safety of ferric carboxymaltose in patients with acute heart failure. AHF-ID study. International journal of clinical practice. 2020 Oct; 74(10):e13584. doi: 10.1111/ijcp.13584. [PMID: 32533907]
  • Hidetomo Kikuchi, Nana Toyoda, Satoko Ezawa, Shiori Yoshida, Yasuhide Hibino, Katsuyoshi Sunaga. Effects of hot‑water extracts from 26 herbs on α‑glucosidase activity. Molecular medicine reports. 2020 Oct; 22(4):3525-3532. doi: 10.3892/mmr.2020.11397. [PMID: 32945423]
  • Yuqi Yang, Yajun Ma, Xiuting Hu, Steve W Cui, Tao Zhang, Ming Miao. Reuteransucrase-catalytic kinetic modeling and functional characteristics for novel prebiotic gluco-oligomers. Food & function. 2020 Aug; 11(8):7037-7047. doi: 10.1039/d0fo00225a. [PMID: 32812985]
  • Ingvar R Möller, Patrick S Merkle, Dionisie Calugareanu, Gerard Comamala, Solveig Gaarde Schmidt, Claus J Loland, Kasper D Rand. Probing the conformational impact of detergents on the integral membrane protein LeuT by global HDX-MS. Journal of proteomics. 2020 08; 225(?):103845. doi: 10.1016/j.jprot.2020.103845. [PMID: 32480080]
  • Nathalie Dautin, Manuela Argentini, Niloofar Mohiman, Cécile Labarre, David Cornu, Laila Sago, Mohamed Chami, Christiane Dietrich, Célia de Sousa d'Auria, Christine Houssin, Muriel Masi, Christophe Salmeron, Nicolas Bayan. Role of the unique, non-essential phosphatidylglycerol::prolipoprotein diacylglyceryl transferase (Lgt) in Corynebacterium glutamicum. Microbiology (Reading, England). 2020 08; 166(8):759-776. doi: 10.1099/mic.0.000937. [PMID: 32490790]
  • I E Emrich, F Lizzi, J D Siegel, S Seiler-Mussler, C Ukena, D Kaddu-Mulindwa, R D'Amelio, S Wagenpfeil, V M Brandenburg, M Böhm, D Fliser, G H Heine. Hypophosphatemia after high-dose iron repletion with ferric carboxymaltose and ferric derisomaltose-the randomized controlled HOMe aFers study. BMC medicine. 2020 07; 18(1):178. doi: 10.1186/s12916-020-01643-5. [PMID: 32654663]
  • Manuela Schoeb, Andrea Räss, Nicola Frei, Stefan Aczél, Michael Brändle, Stefan Bilz. High Risk of Hypophosphatemia in Patients with Previous Bariatric Surgery Receiving Ferric Carboxymaltose: A Prospective Cohort Study. Obesity surgery. 2020 07; 30(7):2659-2666. doi: 10.1007/s11695-020-04544-x. [PMID: 32221822]
  • Wendy Fang, Rachel Kenny, Qurat-Ul-Ain Rizvi, Lawrence P McMahon, Mayur Garg. Hypophosphataemia after ferric carboxymaltose is unrelated to symptoms, intestinal inflammation or vitamin D status. BMC gastroenterology. 2020 Jun; 20(1):183. doi: 10.1186/s12876-020-01298-9. [PMID: 32522150]
  • Betty M Luan-Erfe, Meltem Yilmaz, BobbieJean Sweitzer. Preoperative Intravenous Iron and Erythropoietin to Treat Severe Anemia in Patient With Stage 4 Kidney Disease Before Oncologic Surgery: A Case Report. A&A practice. 2020 Jun; 14(8):e01234. doi: 10.1213/xaa.0000000000001234. [PMID: 32496428]
  • Peter Santer, Anne McGahey, Matthew C Frise, Nayia Petousi, Nick P Talbot, Richard Baskerville, Mona Bafadhel, Annabel H Nickol, Peter A Robbins. Intravenous iron and chronic obstructive pulmonary disease: a randomised controlled trial. BMJ open respiratory research. 2020 06; 7(1):. doi: 10.1136/bmjresp-2020-000577. [PMID: 32565444]
  • Dylan T Wilburn, Steven B Machek, Thomas D Cardaci, Paul S Hwang, Darryn S Willoughby. Acute Maltodextrin Supplementation During Resistance Exercise. Journal of sports science & medicine. 2020 06; 19(2):282-288. doi: . [PMID: 32390721]
  • Shashi Kant, Ravneet Kaur, Farhad Ahamed, Archana Singh, Sumit Malhotra, Rakesh Kumar. Effectiveness of intravenous ferric carboxymaltose in improving hemoglobin level among postpartum women with moderate-to-severe anemia at a secondary care hospital in Faridabad, Haryana - An interventional study. Indian journal of public health. 2020 Apr; 64(2):168-172. doi: 10.4103/ijph.ijph_85_19. [PMID: 32584300]
  • Thanh Phuong Vu, Lili He, David Julian McClements, Eric Andrew Decker. Effects of water activity, sugars, and proteins on lipid oxidative stability of low moisture model crackers. Food research international (Ottawa, Ont.). 2020 04; 130(?):108844. doi: 10.1016/j.foodres.2019.108844. [PMID: 32156340]
  • Junyu Lu, Jingyi Luan, Yijun Li, Xiwen He, Langxing Chen, Yukui Zhang. Hydrophilic maltose-modified magnetic metal-organic framework for highly efficient enrichment of N-linked glycopeptides. Journal of chromatography. A. 2020 Mar; 1615(?):460754. doi: 10.1016/j.chroma.2019.460754. [PMID: 31813565]
  • Yoshihiko Komuro, Takashi Kondo, Shingo Hino, Tatsuya Morita, Naomichi Nishimura. Oral intake of slowly digestible α-glucan, isomaltodextrin, stimulates glucagon-like peptide-1 secretion in the small intestine of rats. The British journal of nutrition. 2020 03; 123(6):619-626. doi: 10.1017/s0007114519003210. [PMID: 31813401]
  • Xiuting Hu, Liping Song, Yuqi Yang, Zhengyu Jin, Ming Miao. Synthesis of potential prebiotic α-glucooligosaccharides using microbial glucansucrase and their in vitro fecal fermentation. Food & function. 2020 Feb; 11(2):1672-1683. doi: 10.1039/c9fo02054c. [PMID: 32031198]
  • Thewika Keeratiburana, Aleksander Riise Hansen, Siriwat Soontaranon, Andreas Blennow, Sunanta Tongta. Porous high amylose rice starch modified by amyloglucosidase and maltogenic α-amylase. Carbohydrate polymers. 2020 Feb; 230(?):115611. doi: 10.1016/j.carbpol.2019.115611. [PMID: 31887905]
  • Myles Wolf, Janet Rubin, Maureen Achebe, Michael J Econs, Munro Peacock, Erik A Imel, Lars L Thomsen, Thomas O Carpenter, Thomas Weber, Vincent Brandenburg, Heinz Zoller. Effects of Iron Isomaltoside vs Ferric Carboxymaltose on Hypophosphatemia in Iron-Deficiency Anemia: Two Randomized Clinical Trials. JAMA. 2020 02; 323(5):432-443. doi: 10.1001/jama.2019.22450. [PMID: 32016310]
  • Srividya Ganapathy, Laura Opdam, Yusaku Hontani, Sean Frehan, Que Chen, Klaas J Hellingwerf, Huub J M de Groot, John T M Kennis, Willem J de Grip. Membrane matters: The impact of a nanodisc-bilayer or a detergent microenvironment on the properties of two eubacterial rhodopsins. Biochimica et biophysica acta. Biomembranes. 2020 02; 1862(2):183113. doi: 10.1016/j.bbamem.2019.183113. [PMID: 31672539]
  • Yanhua Ding, Xiaoxue Zhu, Xiaojiao Li, Hong Zhang, Min Wu, Jingrui Liu, Mary Palmen, Bernard Roubert, Cuiyun Li. Pharmacokinetic, Pharmacodynamic, and Safety Profiles of Ferric Carboxymaltose in Chinese Patients with Iron-deficiency Anemia. Clinical therapeutics. 2020 02; 42(2):276-285. doi: 10.1016/j.clinthera.2019.12.010. [PMID: 31937462]
  • Adrian H Kopf, Jonas M Dörr, Martijn C Koorengevel, Federico Antoniciello, Helene Jahn, J Antoinette Killian. Factors influencing the solubilization of membrane proteins from Escherichia coli membranes by styrene-maleic acid copolymers. Biochimica et biophysica acta. Biomembranes. 2020 02; 1862(2):183125. doi: 10.1016/j.bbamem.2019.183125. [PMID: 31738899]
  • Chunlong Li, Dong Meng, Miguel A Piñeros, Yuxin Mao, Abhaya M Dandekar, Lailiang Cheng. A Sugar Transporter Takes Up both Hexose and Sucrose for Sorbitol-Modulated In Vitro Pollen Tube Growth in Apple. The Plant cell. 2020 02; 32(2):449-469. doi: 10.1105/tpc.19.00638. [PMID: 31826966]
  • Manrong Yu, Hui Chen, Pan Liu, Mei Yang, Leqin Zou, Dingfu Xiao. Antioxidant Function and Metabolomics Study in Mice after Dietary Supplementation with Methionine. BioMed research international. 2020; 2020(?):9494528. doi: 10.1155/2020/9494528. [PMID: 33145362]
  • Juliano Morimoto, Binh Nguyen, Ida Lundbäck, Anh The Than, Shabnam T Tabrizi, Fleur Ponton, Phillip W Taylor. Effects of carbohydrate types on larval development and adult traits in a polyphagous fruit fly. Journal of insect physiology. 2020 01; 120(?):103969. doi: 10.1016/j.jinsphys.2019.103969. [PMID: 31678599]
  • Daniel Edmonston, Myles Wolf. FGF23 at the crossroads of phosphate, iron economy and erythropoiesis. Nature reviews. Nephrology. 2020 01; 16(1):7-19. doi: 10.1038/s41581-019-0189-5. [PMID: 31519999]
  • Lubna Ghani, Chastine F Munk, Xiang Zhang, Satoshi Katsube, Yang Du, Cristina Cecchetti, Weijiao Huang, Hyoung Eun Bae, Savvas Saouros, Muhammad Ehsan, Lan Guan, Xiangyu Liu, Claus J Loland, Brian K Kobilka, Bernadette Byrne, Pil Seok Chae. 1,3,5-Triazine-Cored Maltoside Amphiphiles for Membrane Protein Extraction and Stabilization. Journal of the American Chemical Society. 2019 12; 141(50):19677-19687. doi: 10.1021/jacs.9b07883. [PMID: 31809039]
  • Li Zhang, Xuanfeng Yue, Nan Li, Hailan Shi, Jing Zhang, Zhiqi Zhang, Fuquan Dang. One-step maltose-functionalization of magnetic nanoparticles based on self-assembled oligopeptides for selective enrichment of glycopeptides. Analytica chimica acta. 2019 Dec; 1088(?):63-71. doi: 10.1016/j.aca.2019.08.040. [PMID: 31623717]
  • Vania Manolova, Naja Nyffenegger, Anna Flace, Patrick Altermatt, Ahmet Varol, Cédric Doucerain, Hanna Sundstrom, Franz Dürrenberger. Oral ferroportin inhibitor ameliorates ineffective erythropoiesis in a model of β-thalassemia. The Journal of clinical investigation. 2019 12; 130(1):491-506. doi: 10.1172/jci129382. [PMID: 31638596]
  • Piotr Ponikowski, Bridget-Anne Kirwan, Stefan D Anker, Maria Dorobantu, Jarosław Drozdz, Vincent Fabien, Gerasimos Filippatos, Teba Haboubi, Andre Keren, Irakli Khintibidze, Hans Kragten, Felipe A Martinez, Theresa McDonagh, Marco Metra, Davor Milicic, José C Nicolau, Marcus Ohlsson, Alexander Parhomenko, Domingo A Pascual-Figal, Frank Ruschitzka, David Sim, Hadi Skouri, Peter van der Meer, Ewa A Jankowska. Rationale and design of the AFFIRM-AHF trial: a randomised, double-blind, placebo-controlled trial comparing the effect of intravenous ferric carboxymaltose on hospitalisations and mortality in iron-deficient patients admitted for acute heart failure. European journal of heart failure. 2019 12; 21(12):1651-1658. doi: 10.1002/ejhf.1710. [PMID: 31883356]
  • Carla Rognoni, Vittorio Ortalda, Caterina Biasi, Giovanni Gambaro. Economic Evaluation of Ferric Carboxymaltose for the Management of Hemodialysis Patients with Iron Deficiency Anemia in Italy. Advances in therapy. 2019 11; 36(11):3253-3264. doi: 10.1007/s12325-019-01089-z. [PMID: 31489572]
  • Tsolanku Sidney Maliehe, Albertus Kotze Basson, Nkosinathi Goodman Dlamini. Removal of Pollutants in Mine Wastewater by a Non-Cytotoxic Polymeric Bioflocculant from Alcaligenes faecalis HCB2. International journal of environmental research and public health. 2019 10; 16(20):. doi: 10.3390/ijerph16204001. [PMID: 31635051]
  • Iain C Macdougall. Intravenous Iron Use in the Care of Patients with Kidney Disease. Clinical journal of the American Society of Nephrology : CJASN. 2019 10; 14(10):1528-1530. doi: 10.2215/cjn.00510119. [PMID: 31175103]
  • Kübra Ertan, Meltem Türkyılmaz, Mehmet Özkan. Effects of natural copigment sources in combination with sweeteners on the stability of anthocyanins in sour cherry nectars. Food chemistry. 2019 Oct; 294(?):423-432. doi: 10.1016/j.foodchem.2019.05.089. [PMID: 31126483]
  • Hongjuan Li, Hongmei Yu, Yan Liu, Yi Wang, Hongbo Li, Jinghua Yu. The use of of inulin, maltitol and lecithin as fat replacers and plasticizers in a model reduced-fat mozzarella cheese-like product. Journal of the science of food and agriculture. 2019 Sep; 99(12):5586-5593. doi: 10.1002/jsfa.9835. [PMID: 31152446]
  • Darlington O Okonko, Fadi Jouhra, Huda Abu-Own, Gerasimos Filippatos, Josep Comin Colet, Chainey Suki, Claudio Mori, Piotr Ponikowski, Stefan D Anker. Effect of ferric carboxymaltose on calculated plasma volume status and clinical congestion: a FAIR-HF substudy. ESC heart failure. 2019 08; 6(4):621-628. doi: 10.1002/ehf2.12462. [PMID: 31148411]
  • Manuel Muñoz, Peter Skov Olsen, Tonny Studsgaard Petersen, Susanne Manhart, Stig Waldorff. Pharmacokinetics of ferric bepectate-a new intravenous iron drug for treating iron deficiency. Basic & clinical pharmacology & toxicology. 2019 Aug; 125(2):133-141. doi: 10.1111/bcpt.13219. [PMID: 30839153]
  • Philip Krieter, Shwe Gyaw, C Nora Chiang, Roger Crystal, Phil Skolnick. Enhanced Intranasal Absorption of Naltrexone by Dodecyl Maltopyranoside: Implications for the Treatment of Opioid Overdose. Journal of clinical pharmacology. 2019 07; 59(7):947-957. doi: 10.1002/jcph.1384. [PMID: 30698833]
  • Thierry Romanet, Pierrick Bedouch, Philippe Zaoui. [Assessment of iron deficiency anemia management in the general hospital of Grenoble: A 12-month follow-up of an intravenous ferric carboxymaltose treatment program in a cohort of patients with non-dialysis-dependent chronic kidney disease]. Nephrologie & therapeutique. 2019 Apr; 15(2):104-109. doi: 10.1016/j.nephro.2018.10.006. [PMID: 30803900]
  • Ranjana Das, Arvind M Kayastha. Enzymatic hydrolysis of native granular starches by a new β-amylase from peanut (Arachis hypogaea). Food chemistry. 2019 Mar; 276(?):583-590. doi: 10.1016/j.foodchem.2018.10.058. [PMID: 30409636]
  • Rizliya Visvanathan, Chathuni Jayathilake, Ruvini Liyanage, Ramiah Sivakanesan. Applicability and reliability of the glucose oxidase method in assessing α-amylase activity. Food chemistry. 2019 Mar; 275(?):265-272. doi: 10.1016/j.foodchem.2018.09.114. [PMID: 30724196]
  • Matthias Diebold, Andreas D Kistler. Evaluation of iron stores in hemodialysis patients on maintenance ferric Carboxymaltose dosing. BMC nephrology. 2019 03; 20(1):76. doi: 10.1186/s12882-019-1263-8. [PMID: 30823916]
  • Ke Wang, Tingting Qi, Longcheng Guo, Zhongxuan Ma, Guofeng Gu, Min Xiao, Lili Lu. Enzymatic Glucosylation of Salidroside from Starch by α-Amylase. Journal of agricultural and food chemistry. 2019 Feb; 67(7):2012-2019. doi: 10.1021/acs.jafc.8b06618. [PMID: 30678460]
  • Carolina Shene, Marcelo Garcés, Daniela Vergara, Jhonatan Peña, Stéphane Claverol, Mónica Rubilar, Allison Leyton. Production of Lipids and Proteome Variation in a Chilean Thraustochytrium striatum Strain Cultured under Different Growth Conditions. Marine biotechnology (New York, N.Y.). 2019 Feb; 21(1):99-110. doi: 10.1007/s10126-018-9863-z. [PMID: 30456696]
  • Takayuki Hamano. [The beneficial effects of iron supplementation other than improvement of anemia]. [Rinsho ketsueki] The Japanese journal of clinical hematology. 2019; 60(9):1092-1099. doi: 10.11406/rinketsu.60.1092. [PMID: 31597832]
  • Bernardo Faria, Mariana Gaya da Costa, Felix Poppelaars, Casper F M Franssen, Manuel Pestana, Stefan P Berger, Mohamed R Daha, Carlo A J M Gaillard, Marc A Seelen. Administration of Intravenous Iron Formulations Induces Complement Activation in-vivo. Frontiers in immunology. 2019; 10(?):1885. doi: 10.3389/fimmu.2019.01885. [PMID: 31497011]
  • David Calderón Guzmán, Norma Osnaya Brizuela, Maribel Ortíz Herrera, Hugo Juárez Olguín, Armando Valenzuela Peraza, Ernestina Hernández García, Francisca Trujillo Jiménez, Gerardo Barragán Mejía. Cytarabine and Ferric Carboxymaltose (Fe+3) Increase Oxidative Damage and Alter Serotonergic Metabolism in Brain. CNS & neurological disorders drug targets. 2019; 18(2):149-155. doi: 10.2174/1871527318666181128144343. [PMID: 30484410]