S-adenosylhomocysteine (SAH) (BioDeep_00000001428)

 

Secondary id: BioDeep_00000400261

natural product human metabolite PANOMIX_OTCML-2023 Endogenous blood metabolite BioNovoGene_Lab2019


代谢物信息卡片


(2S)-2-Amino-4-({[(2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl}sulphanyl)butanoic acid

化学式: C14H20N6O5S (384.1216)
中文名称: S-(5'-腺苷)-L-高半胱氨酸, S-(5’-腺苷)-L-高半胱氨酸, 腺苷高半胱氨酸, S-腺苷-高半胱氨酸
谱图信息: 最多检出来源 Homo sapiens(feces) 22.31%

Reviewed

Last reviewed on 2024-09-13.

Cite this Page

S-adenosylhomocysteine (SAH). BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China. https://query.biodeep.cn/s/s-adenosylhomocysteine_(sah) (retrieved 2024-12-22) (BioDeep RN: BioDeep_00000001428). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

分子结构信息

SMILES: C(CSC[C@@H]1[C@H]([C@H]([C@H](n2cnc3c(N)ncnc23)O1)O)O)[C@@H](C(=O)O)N
InChI: InChI=1S/C14H20N6O5S/c15-6(14(23)24)1-2-26-3-7-9(21)10(22)13(25-7)20-5-19-8-11(16)17-4-18-12(8)20/h4-7,9-10,13,21-22H,1-3,15H2,(H,23,24)(H2,16,17,18)/t6-,7+,9+,10+,13+/m0/s1

描述信息

S-Adenosyl-L-homocysteine (SAH) is formed by the demethylation of S-adenosyl-L-methionine. S-Adenosylhomocysteine (AdoHcy or SAH) is also the immediate precursor of all of the homocysteine produced in the body. The reaction is catalyzed by S-adenosylhomocysteine hydrolase and is reversible with the equilibrium favoring formation of SAH. In vivo, the reaction is driven in the direction of homocysteine formation by the action of the enzyme adenosine deaminase which converts the second product of the S-adenosylhomocysteine hydrolase reaction, adenosine, to inosine. Except for methyl transfer from betaine and from methylcobalamin in the methionine synthase reaction, SAH is the product of all methylation reactions that involve S-adenosylmethionine (SAM) as the methyl donor. Methylation is significant in epigenetic regulation of protein expression via DNA and histone methylation. The inhibition of these SAM-mediated processes by SAH is a proven mechanism for metabolic alteration. Because the conversion of SAH to homocysteine is reversible, with the equilibrium favoring the formation of SAH, increases in plasma homocysteine are accompanied by an elevation of SAH in most cases. Disturbances in the transmethylation pathway indicated by abnormal SAH, SAM, or their ratio have been reported in many neurodegenerative diseases, such as dementia, depression, and Parkinsons disease (PMID:18065573, 17892439). Therefore, when present in sufficiently high levels, S-adenosylhomocysteine can act as an immunotoxin and a metabotoxin. An immunotoxin disrupts, limits the function, or destroys immune cells. A metabotoxin is an endogenous metabolite that causes adverse health effects at chronically high levels. Chronically high levels of S-adenosylhomocysteine are associated with S-adenosylhomocysteine (SAH) hydrolase deficiency and adenosine deaminase deficiency. S-Adenosylhomocysteine forms when there are elevated levels of homocysteine and adenosine. S-Adenosyl-L-homocysteine is a potent inhibitor of S-adenosyl-L-methionine-dependent methylation reactions. It is toxic to immature lymphocytes and can lead to immunosuppression (PMID:221926).
S-adenosylhomocysteine, also known as adohcy or sah, is a member of the class of compounds known as 5-deoxy-5-thionucleosides. 5-deoxy-5-thionucleosides are 5-deoxyribonucleosides in which the ribose is thio-substituted at the 5position by a S-alkyl group. S-adenosylhomocysteine is slightly soluble (in water) and a moderately acidic compound (based on its pKa). S-adenosylhomocysteine can be found in a number of food items such as rapini, european plum, rambutan, and pepper (c. pubescens), which makes S-adenosylhomocysteine a potential biomarker for the consumption of these food products. S-adenosylhomocysteine can be found primarily in blood, cerebrospinal fluid (CSF), feces, and urine, as well as throughout most human tissues. S-adenosylhomocysteine exists in all living species, ranging from bacteria to humans. In humans, S-adenosylhomocysteine is involved in several metabolic pathways, some of which include phosphatidylcholine biosynthesis PC(14:0/18:3(9Z,12Z,15Z)), phosphatidylcholine biosynthesis PC(22:4(7Z,10Z,13Z,16Z)/22:0), phosphatidylcholine biosynthesis PC(20:3(5Z,8Z,11Z)/22:2(13Z,16Z)), and phosphatidylcholine biosynthesis PC(18:3(6Z,9Z,12Z)/22:5(7Z,10Z,13Z,16Z,19Z)). S-adenosylhomocysteine is also involved in several metabolic disorders, some of which include 3-phosphoglycerate dehydrogenase deficiency, hawkinsinuria, non ketotic hyperglycinemia, and tyrosine hydroxylase deficiency. Moreover, S-adenosylhomocysteine is found to be associated with neurodegenerative disease and parkinsons disease. S-adenosylhomocysteine is a non-carcinogenic (not listed by IARC) potentially toxic compound. S-Adenosyl-L-homocysteine (SAH) is an amino acid derivative used in several metabolic pathways in most organisms. It is an intermediate in the synthesis of cysteine and adenosine .
[Spectral] S-Adenosyl-L-homocysteine (exact mass = 384.12159) and Adenosine (exact mass = 267.09675) were not completely separated on HPLC under the present analytical conditions as described in AC$XXX. Additionally some of the peaks in this data contains dimers and other unidentified ions.
[Spectral] S-Adenosyl-L-homocysteine (exact mass = 384.12159) and Cytidine (exact mass = 243.08552) were not completely separated on HPLC under the present analytical conditions as described in AC$XXX. Additionally some of the peaks in this data contains dimers and other unidentified ions.
Acquisition and generation of the data is financially supported in part by CREST/JST.
COVID info from PDB, Protein Data Bank, WikiPathways
Corona-virus
Coronavirus
SARS-CoV-2
COVID-19
SARS-CoV
COVID19
SARS2
SARS
SAH (S-Adenosylhomocysteine) is an amino acid derivative and a modulartor in several metabolic pathways. It is an intermediate in the synthesis of cysteine and adenosine[1]. SAH is an inhibitor for METTL3-METTL14 heterodimer complex (METTL3-14) with an IC50 of 0.9 μM[2].
SAH (S-Adenosylhomocysteine) is an amino acid derivative and a modulartor in several metabolic pathways. It is an intermediate in the synthesis of cysteine and adenosine[1]. SAH is an inhibitor for METTL3-METTL14 heterodimer complex (METTL3-14) with an IC50 of 0.9 μM[2].

同义名列表

33 个代谢物同义名

(2S)-2-Amino-4-({[(2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl}sulphanyl)butanoic acid; (2S)-2-Amino-4-({[(2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl}sulfanyl)butanoic acid; (2S)-2-Amino-4-({[(2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl}sulphanyl)butanoate; (2S)-2-Amino-4-({[(2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl}sulfanyl)butanoate; (2S)-2-amino-4-({[(2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl}sulfanyl)butanoic acid; S-[1-(Adenin-9-yl)-1,5-dideoxy-beta-D-ribofuranos-5-yl]-L-homocysteine; S-[1-(Adenin-9-yl)-1,5-dideoxy-b-D-ribofuranos-5-yl]-L-homocysteine; S-[1-(Adenin-9-yl)-1,5-dideoxy-β-D-ribofuranos-5-yl]-L-homocysteine; (S)-5-(S)-(3-Amino-3-carboxypropyl)-5-thioadenosine; L-5-S-(3-Amino-3-carboxypropyl)-5-thior-adenosine; 5-S-(3-Amino-3-carboxypropyl)-5-thio-L-adenosine; S-(5-Deoxyadenosin-5-yl)-L-homocysteine; S-(5-Deoxyadenosine-5)-L-homocysteine; 5-Deoxy-S-adenosyl-L-homocysteine; S-(5-Adenosyl)-L-homocysteine; 2-S-Adenosyl-L-homocysteine; S-Adenosyl-L-homocysteine; L-S-Adenosyl-homocysteine; L-S-Adenosylhomocysteine; Adenosyl-L-homocysteine; S-Adenosyl-homocysteine; Adenosylhomocysteine, S; Formycinylhomocysteine; S-Adenosylhomocysteine; S Adenosylhomocysteine; Adenosylhomocysteine; Adenosyl-homo-cys; Adenosylhomo-cys; AdoHcy; SAH; S-Adenosylhomocysteine; SAH (S-Adenosylhomocysteine); S-Adenosyl-L-homocysteine



数据库引用编号

50 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(17)

BioCyc(9)

PlantCyc(0)

代谢反应

1222 个相关的代谢反应过程信息。

Reactome(313)

BioCyc(21)

WikiPathways(15)

Plant Reactome(865)

INOH(7)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(1)

1 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 10 ADA, AHCY, AHCYL1, APOE, CASP3, CBS, DNMT3A, GNMT, MTR, PNP
Peripheral membrane protein 2 ADA, AHCYL1
Endoplasmic reticulum membrane 3 AHCYL1, PEMT, PNMT
Mitochondrion membrane 2 PEMT, PNMT
Nucleus 8 ADK, AHCY, APOE, BHMT, CASP3, CBS, DNMT1, DNMT3A
cytosol 15 ADA, ADK, AHCY, AHCYL1, BHMT, CASP3, CBS, COMT, GNMT, MAT1A, MTHFR, MTR, PEMT, PNMT, PNP
dendrite 2 APOE, COMT
mitochondrial membrane 2 PEMT, PNMT
nucleoplasm 4 ADK, CASP3, DNMT1, DNMT3A
Cell membrane 3 ADA, COMT, TNF
Multi-pass membrane protein 2 PEMT, PNMT
Synapse 1 COMT
cell junction 1 ADA
cell surface 2 ADA, TNF
glutamatergic synapse 2 APOE, CASP3
Golgi apparatus 1 APOE
Golgi membrane 1 INS
neuronal cell body 3 APOE, CASP3, TNF
Cytoplasm, cytosol 2 AHCYL1, BHMT
Lysosome 1 ADA
plasma membrane 5 ADA, ADK, APOE, COMT, TNF
Membrane 4 ADA, APOE, COMT, PEMT
apical plasma membrane 1 AHCYL1
axon 1 COMT
extracellular exosome 6 AHCY, AHCYL1, APOE, BHMT, COMT, PNP
endoplasmic reticulum 5 AHCY, AHCYL1, APOE, PEMT, PNMT
extracellular space 4 APOE, INS, PNP, TNF
mitochondrion 3 DNMT1, PEMT, PNMT
intracellular membrane-bounded organelle 3 COMT, PEMT, PNMT
postsynaptic density 1 CASP3
pericentric heterochromatin 1 DNMT1
Secreted 3 APOE, INS, PNP
extracellular region 4 APOE, INS, PNP, TNF
Extracellular side 2 ADA, COMT
Cytoplasmic vesicle lumen 1 ADA
anchoring junction 1 ADA
external side of plasma membrane 2 ADA, TNF
Endosome, multivesicular body 1 APOE
Extracellular vesicle 1 APOE
Secreted, extracellular space, extracellular matrix 1 APOE
chylomicron 1 APOE
high-density lipoprotein particle 1 APOE
low-density lipoprotein particle 1 APOE
multivesicular body 1 APOE
very-low-density lipoprotein particle 1 APOE
Early endosome 1 APOE
recycling endosome 1 TNF
Single-pass type II membrane protein 2 COMT, TNF
Apical cell membrane 1 AHCYL1
heterochromatin 1 DNMT3A
Membrane raft 1 TNF
extracellular matrix 1 APOE
collagen-containing extracellular matrix 1 APOE
phagocytic cup 1 TNF
Chromosome 1 DNMT3A
Secreted, extracellular space 1 APOE
blood microparticle 1 APOE
endosome lumen 1 INS
female germ cell nucleus 1 DNMT1
mitochondria-associated endoplasmic reticulum membrane contact site 1 AHCYL1
[Isoform 1]: Endoplasmic reticulum membrane 2 PEMT, PNMT
Melanosome 2 AHCY, APOE
euchromatin 1 DNMT3A
replication fork 1 DNMT1
Microsome 1 AHCYL1
ficolin-1-rich granule lumen 1 PNP
secretory granule lumen 2 INS, PNP
Golgi lumen 1 INS
endoplasmic reticulum lumen 2 APOE, INS
nuclear matrix 1 DNMT3A
XY body 1 DNMT3A
transport vesicle 1 INS
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
chromosome, centromeric region 1 DNMT3A
[Isoform 2]: Cytoplasm 1 ADK
clathrin-coated endocytic vesicle membrane 1 APOE
[Isoform 1]: Nucleus 1 ADK
synaptic cleft 1 APOE
death-inducing signaling complex 1 CASP3
[Isoform 2]: Endoplasmic reticulum membrane 2 PEMT, PNMT
discoidal high-density lipoprotein particle 1 APOE
endocytic vesicle lumen 1 APOE
[Tumor necrosis factor, soluble form]: Secreted 1 TNF
chylomicron remnant 1 APOE
intermediate-density lipoprotein particle 1 APOE
lipoprotein particle 1 APOE
multivesicular body, internal vesicle 1 APOE
catalytic complex 1 DNMT3A
[Isoform Soluble]: Cytoplasm 1 COMT
[Isoform Membrane-bound]: Cell membrane 1 COMT
methionine adenosyltransferase complex 1 MAT1A
[C-domain 2]: Secreted 1 TNF
[Tumor necrosis factor, membrane form]: Membrane 1 TNF
[C-domain 1]: Secreted 1 TNF


文献列表

  • Xin Dai, Si Liu, Lokyu Cheng, Ting Huang, Honghui Guo, Dongliang Wang, Min Xia, Wenhua Ling, Yunjun Xiao. Epigenetic Upregulation of H19 and AMPK Inhibition Concurrently Contribute to S-Adenosylhomocysteine Hydrolase Deficiency-Promoted Atherosclerotic Calcification. Circulation research. 2022 05; 130(10):1565-1582. doi: 10.1161/circresaha.121.320251. [PMID: 35410483]
  • Carolyn F McCabe, Jennifer L LaBarre, Steven E Domino, Marjorie C Treadwell, Ana Baylin, Charles F Burant, Dana C Dolinoy, Vasantha Padmanabhan, Jaclyn M Goodrich. Maternal and neonatal one-carbon metabolites and the epigenome-wide infant response. The Journal of nutritional biochemistry. 2022 03; 101(?):108938. doi: 10.1016/j.jnutbio.2022.108938. [PMID: 35017001]
  • Si Liu, Ruyi Liao, Xin Dai, Honghui Guo, Dongliang Wang, Min Xia, Wenhua Ling, Yunjun Xiao. Association between plasma S-adenosylmethionine and risk of mortality in patients with coronary artery disease: A cohort study. The American journal of clinical nutrition. 2021 10; 114(4):1360-1370. doi: 10.1093/ajcn/nqab210. [PMID: 34192296]
  • Madan Kumar Arumugam, Srinivas Chava, Karuna Rasineni, Matthew C Paal, Terrence M Donohue, Natalia A Osna, Kusum K Kharbanda. Elevated S-adenosylhomocysteine induces adipocyte dysfunction to promote alcohol-associated liver steatosis. Scientific reports. 2021 07; 11(1):14693. doi: 10.1038/s41598-021-94180-x. [PMID: 34282217]
  • Jacob Joseph, Anna Giczewska, Brooke Alhanti, Amrita K Cheema, Diane E Handy, Douglas L Mann, Joseph Loscalzo, Michael M Givertz. Associations of methyl donor and methylation inhibitor levels during anti-oxidant therapy in heart failure. Journal of physiology and biochemistry. 2021 May; 77(2):295-304. doi: 10.1007/s13105-021-00797-x. [PMID: 33595776]
  • Maria Petrovna Kruglova, Alexander Vladimirovich Ivanov, Edward Danielevich Virus, Polina Olegovna Bulgakova, Andrey Segeevich Samokhin, Anatolij Nikolaevich Fedoseev, Sergej Vital'evich Grachev, Aslan Amirkhanovich Kubatiev. Urine S-Adenosylmethionine are Related to Degree of Renal Insufficiency in Patients with Chronic Kidney Disease. Laboratory medicine. 2021 Jan; 52(1):47-56. doi: 10.1093/labmed/lmaa034. [PMID: 32702115]
  • Evgeny Vladimirovich Kryukov, Alexander Vladimirovich Ivanov, Vladimir Olegovich Karpov, Valery Vasil'evich Aleksandrin, Alexander Mikhaylovich Dygai, Maria Petrovna Kruglova, Gennady Ivanovich Kostiuchenko, Sergei Petrovich Kazakov, Aslan Amirkhanovich Kubatiev. Plasma S-Adenosylmethionine Is Associated with Lung Injury in COVID-19. Disease markers. 2021; 2021(?):7686374. doi: 10.1155/2021/7686374. [PMID: 34956420]
  • George Stojan, Jessica Li, Tian Liu, Maureen A Kane, Michelle A Petri. Intracellular homocysteine metabolites in SLE: plasma S-adenosylhomocysteine correlates with coronary plaque burden. Lupus science & medicine. 2021 01; 8(1):. doi: 10.1136/lupus-2020-000453. [PMID: 33479047]
  • Sally P Stabler. Alterations in Sulfur Amino Acids as Biomarkers of Disease. The Journal of nutrition. 2020 10; 150(Suppl 1):2532S-2537S. doi: 10.1093/jn/nxaa118. [PMID: 33000156]
  • Monica Rosas-Lemus, George Minasov, Ludmilla Shuvalova, Nicole L Inniss, Olga Kiryukhina, Joseph Brunzelle, Karla J F Satchell. High-resolution structures of the SARS-CoV-2 2'-O-methyltransferase reveal strategies for structure-based inhibitor design. Science signaling. 2020 09; 13(651):. doi: 10.1126/scisignal.abe1202. [PMID: 32994211]
  • Rostom Ahmed-Belkacem, Priscila Sutto-Ortiz, Mathis Guiraud, Bruno Canard, Jean-Jacques Vasseur, Etienne Decroly, Françoise Debart. Synthesis of adenine dinucleosides SAM analogs as specific inhibitors of SARS-CoV nsp14 RNA cap guanine-N7-methyltransferase. European journal of medicinal chemistry. 2020 Sep; 201(?):112557. doi: 10.1016/j.ejmech.2020.112557. [PMID: 32563813]
  • Madan Kumar Arumugam, Sharanappa Talawar, Laura Listenberger, Terrence M Donohue, Natalia A Osna, Kusum K Kharbanda. Role of Elevated Intracellular S-Adenosylhomocysteine in the Pathogenesis of Alcohol-Related Liver Disease. Cells. 2020 06; 9(6):. doi: 10.3390/cells9061526. [PMID: 32585865]
  • Shu-Fei Zhang, Xin-Jing Mao, Wei-Min Jiang, Zhu-Yuan Fang. Qian Yang Yu Yin Granule protects against hypertension-induced renal injury by epigenetic mechanism linked to Nicotinamide N-Methyltransferase (NNMT) expression. Journal of ethnopharmacology. 2020 Jun; 255(?):112738. doi: 10.1016/j.jep.2020.112738. [PMID: 32147479]
  • Alexander Vladimirovich Ivanov, Mariya Petrovna Kruglova, Edward Danielevich Virus, Polina Olegovna Bulgakova, Sergei Vital'evich Grachev, Aslan Amirkhanovich Kubatiev. Determination of S-adenosylmethionine, S-adenosylhomocysteine, and methylthioadenosine in urine using solvent-modified micellar electrokinetic chromatography. Electrophoresis. 2020 02; 41(3-4):209-214. doi: 10.1002/elps.201900364. [PMID: 31779046]
  • Maria Petrovna Kruglova, Sergej Vital'evich Grachev, Polina Olegovna Bulgakova, Alexander Vladimirovich Ivanov, Edward Danielevich Virus, Ksenya Alexandrovna Nikiforova, Anatolij Nikolaevich Fedoseev, Galina Dmitrievna Savina, Aslan Amirkhanovich Kubatiev. Low S-adenosylmethionine/ S-adenosylhomocysteine Ratio in Urine is Associated with Chronic Kidney Disease. Laboratory medicine. 2020 Jan; 51(1):80-85. doi: 10.1093/labmed/lmz035. [PMID: 31247080]
  • Alexander Vladimirovich Ivanov, Ekaterina Alexandrovna Dubchenko, Maria Petrovna Kruglova, Edward Danielevich Virus, Polina Olegovna Bulgakova, Valery Vasil'evich Alexandrin, Anatolij Nikolaevich Fedoseev, Alexey Nikolaevich Boyko, Sergej Vitalievich Grachev, Aslan Amirkhanovich Kubatiev. Determination of S-adenosylmethionine and S-adenosylhomocysteine in blood plasma by UPLC with fluorescence detection. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2019 Aug; 1124(?):366-374. doi: 10.1016/j.jchromb.2019.06.032. [PMID: 31295723]
  • Baiyi Li, Shaoyan Chang, Chi Liu, Min Zhang, Lianfeng Zhang, Liang Liang, Rui Li, Xiuwei Wang, Chuan Qin, Ting Zhang, Bo Niu, Li Wang. Low Maternal Dietary Folate Alters Retrotranspose by Methylation Regulation in Intrauterine Growth Retardation (IUGR) Fetuses in a Mouse Model. Medical science monitor : international medical journal of experimental and clinical research. 2019 May; 25(?):3354-3365. doi: 10.12659/msm.914292. [PMID: 31061382]
  • Yunjun Xiao, Junjie Xia, Jinquan Cheng, Haiyan Huang, Yani Zhou, Xifei Yang, Xuefen Su, Yuebin Ke, Wenhua Ling. Inhibition of S-Adenosylhomocysteine Hydrolase Induces Endothelial Dysfunction via Epigenetic Regulation of p66shc-Mediated Oxidative Stress Pathway. Circulation. 2019 05; 139(19):2260-2277. doi: 10.1161/circulationaha.118.036336. [PMID: 30773021]
  • Alexandra Schutkowski, Bettina König, Holger Kluge, Frank Hirche, Andrea Henze, Tanja Schwerdtle, Stefan Lorkowski, Christine Dawczynski, Alexander Gabel, Ivo Große, Gabriele I Stangl. Metabolic footprint and intestinal microbial changes in response to dietary proteins in a pig model. The Journal of nutritional biochemistry. 2019 05; 67(?):149-160. doi: 10.1016/j.jnutbio.2019.02.004. [PMID: 30925412]
  • Sandra G Heil, Emilie M Herzog, Pieter H Griffioen, Bertrand van Zelst, Sten P Willemsen, Yolanda B de Rijke, Regine P M Steegers-Theunissen, Eric A P Steegers. Lower S-adenosylmethionine levels and DNA hypomethylation of placental growth factor (PlGF) in placental tissue of early-onset preeclampsia-complicated pregnancies. PloS one. 2019; 14(12):e0226969. doi: 10.1371/journal.pone.0226969. [PMID: 31887212]
  • Zetao Bai, Tianxiong Qi, Yuchen Liu, Zhenying Wu, Lichao Ma, Wenwen Liu, Yingping Cao, Yan Bao, Chunxiang Fu. Alteration of S-adenosylhomocysteine levels affects lignin biosynthesis in switchgrass. Plant biotechnology journal. 2018 12; 16(12):2016-2026. doi: 10.1111/pbi.12935. [PMID: 29704888]
  • Hussain Mohamad Awwad, Carsten-Henning Ohlmann, Michael Stoeckle, Juergen Geisel, Rima Obeid. Serum concentrations of folate vitamers in patients with a newly diagnosed prostate cancer or hyperplasia. Clinical biochemistry. 2018 Jun; 56(?):41-46. doi: 10.1016/j.clinbiochem.2018.04.011. [PMID: 29673813]
  • Myriam Visram, Maja Radulovic, Sabine Steiner, Nermina Malanovic, Thomas O Eichmann, Heimo Wolinski, Gerald N Rechberger, Oksana Tehlivets. Homocysteine regulates fatty acid and lipid metabolism in yeast. The Journal of biological chemistry. 2018 04; 293(15):5544-5555. doi: 10.1074/jbc.m117.809236. [PMID: 29414770]
  • Karen E Christensen, Renata H Bahous, Wenyang Hou, Liyuan Deng, Olga V Malysheva, Erland Arning, Teodoro Bottiglieri, Marie A Caudill, Loydie A Jerome-Majewska, Rima Rozen. Low Dietary Folate Interacts with MTHFD1 Synthetase Deficiency in Mice, a Model for the R653Q Variant, to Increase Incidence of Developmental Delays and Defects. The Journal of nutrition. 2018 04; 148(4):501-509. doi: 10.1093/jn/nxy013. [PMID: 29659962]
  • M V Lind, L Lauritzen, H Vestergaard, T Hansen, O Pedersen, M Kristensen, A B Ross. One-carbon metabolism markers are associated with cardiometabolic risk factors. Nutrition, metabolism, and cardiovascular diseases : NMCD. 2018 04; 28(4):402-410. doi: 10.1016/j.numecd.2018.01.005. [PMID: 29499850]
  • Ruben Esse, Tom Teerlink, Pieter Koolwijk, Isabel Tavares de Almeida, Henk J Blom, Rita Castro. Folinic Acid Increases Protein Arginine Methylation in Human Endothelial Cells. Nutrients. 2018 Mar; 10(4):. doi: 10.3390/nu10040404. [PMID: 29587354]
  • Diogo Farias Riberio, Paola Sanchez Cella, Lilian Eslaine Costa Mendes da Silva, Alceu Afonso Jordao, Rafael Deminice. Acute exercise alters homocysteine plasma concentration in an intensity-dependent manner due increased methyl flux in liver of rats. Life sciences. 2018 Mar; 196(?):63-68. doi: 10.1016/j.lfs.2018.01.003. [PMID: 29307522]
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