Zobrazeno 1 - 10
of 53
pro vyhledávání: '"MTHFR, methylenetetrahydrofolate reductase"'
Autor:
Hansashree Padmanabha, Rohan Mahale, Rita Christopher, Gautham Arunachal, Maya Bhat, Mahammad Samim Mondal, Ram Murthy Anjanappa, Ravindranadh Chowdhary Mundlamuri, Ravi Yadav, Seena Vengalil, Pooja Mailankody, Pavagada S Mathuranath, Sadanandavalli R Chandra, Atchayaram Nalini
Publikováno v:
Annals of Indian Academy of Neurology, Vol 24, Iss 6, Pp 908-916 (2021)
Objectives: The objective of this study is to describe the clinical, biochemical, radiological, and genetic profile of patients presenting with progressive spastic paraparesis due to homocysteine remethylation pathway defect. Methods: This was a retr
Externí odkaz:
https://doaj.org/article/3d27f9d8a8d74fccb2d9f75e0a83f78f
Publikováno v:
JAAD Case Reports
JAAD Case Reports, Vol 11, Iss, Pp 47-50 (2021)
JAAD Case Reports, Vol 11, Iss, Pp 47-50 (2021)
Autor:
Jansen Gerrit, Weijers Karin, Blits Marjolein, van der Heijden Joost, Gent Yoony, Al Marjon, van der Laken Conny, Molthoff Carla, Verweij Cor, Voskuijl Alexandre, Lems Willem, Scheper Rik, Peters Godefridus, Ratnam Manohar, Aassaraf Yehuda, Dijkmans Ben
Publikováno v:
Pteridines, Vol 24, Iss 1, Pp 21-26 (2013)
Almost all current standard treatment of care for patients with chronic inflammatory diseases such as rheumatoid arthritis (RA) includes the folate antagonist methotrexate (MTX). Despite the proven efficacy of MTX in RA treatment, it is anticipated t
Externí odkaz:
https://doaj.org/article/e593d5a56a1546ec9a04bf4a34f6331d
109 sick with migraine are clinical neurologically examined, which were divided into 2 groups: the first group sick with migraine with aura (n - 22); the second group - sick with migraine without aura (n - 87). In addition, a PCR (polymerase chain re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ab53007cb8b9852a2795382bbe7e610
Autor:
Atchayaram Nalini, Hansashree Padmanabha, Rohan Mahale, Rita Christopher, Gautham Arunachal, Maya Bhat, MahammadSamim Mondal, RamMurthy Anjanappa, RavindranadhChowdhary Mundlamuri, Ravi Yadav, Seena Vengalil, Pooja Mailankody, PavagadaS Mathuranath, SadanandavalliR Chandra
Publikováno v:
Annals of Indian Academy of Neurology, Vol 24, Iss 6, Pp 908-916 (2021)
Objectives: The objective of this study is to describe the clinical, biochemical, radiological, and genetic profile of patients presenting with progressive spastic paraparesis due to homocysteine remethylation pathway defect. Methods: This was a retr
Publikováno v:
Epilepsy & Behavior Reports, Vol 15, Iss, Pp 100419-(2021)
Epilepsy & Behavior Reports
Epilepsy & Behavior Reports
Highlights • Folate processing gene (MTHFR) defects are common in women with epilepsy (WWE) and mood disorders. • Methylated versions of folate and B12 may bypass problems related to MTHFR gene processing. • Successful pregnancies occurred in W
Autor:
Alice P. Sowton, Andrew J. Murray, Simon James Tunster, Erica D. Watson, Ben D. McNally, Nisha Padmanabhan, Julian L. Griffin, Antonio Murgia, Aisha Yusuf
Publikováno v:
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 23, Iss, Pp-(2020)
Molecular Genetics and Metabolism Reports, Vol 23, Iss, Pp-(2020)
Nonalcoholic fatty liver disease (NAFLD) is associated with dietary folate deficiency and mutations in genes required for one‑carbon metabolism. However, the mechanism through which this occurs is unclear. To improve our understanding of this link,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5de79e1f7ef67cef5ce425b58d812c6
http://hdl.handle.net/10044/1/82233
http://hdl.handle.net/10044/1/82233
Publikováno v:
Molecular Genetics and Metabolism Reports, 22
Molecular Genetics and Metabolism Reports 22 (2020)
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 22, Iss, Pp-(2020)
Molecular Genetics and Metabolism Reports 22 (2020)
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 22, Iss, Pp-(2020)
Background: Elevated homocysteine (Hcy) is associated with several pathologies. Gene–diet interactions related to Hcy might be used to customize dietary advice to reduce disease incidence. To explore this possibility, we investigated interactions b
Akademický článek
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Publikováno v:
Meta Gene
Background Glutathione S-transferases (GSTM1, GSTT1, and GSTP1) and methylenetetrahydrofolate reductase (MTHFR) are important enzymes for protection against oxidative stress. In addition, MTHFR has an essential role in DNA synthesis, repair, and meth