Zobrazeno 1 - 10
of 946
pro vyhledávání: '"methionine synthase reductase"'
Autor:
Zhang, Wei1, Zhang, Ze2, Wu, Hao2, Xu, Kai2, Yuan, Wei3, Mi, Yuan-Yuan4, Shi, Li2 rock200x@126.com, Zuo, Li2 jiaomin0324@126.com, Shi, Yun-Feng5,6 fzy8353@163.com
Publikováno v:
Scientific Reports. 8/7/2020, Vol. 10 Issue 1, p1-12. 12p.
Autor:
Deobald, Darja1,2, Hanna, Rafael1,3, Shahryari, Shahab2, Layer, Gunhild1,3, Adrian, Lorenz2,4 lorenz.adrian@ufz.de
Publikováno v:
Scientific Reports. 2/7/2020, Vol. 10 Issue 1, p1-13. 13p.
Autor:
Alexandre Nguyen, Samuel Deshayes, Marie Nowoczyn, Apolline Imbard, Lamisse Mansour‐Hendili, Alexandre Cesbron, Jean François Benoist, Manuel Schiff
Publikováno v:
JIMD Reports, Vol 65, Iss 3, Pp 163-170 (2024)
Abstract Methionine synthase reductase deficiency (cblE) is a rare autosomal recessive inborn error of cobalamin metabolism caused by pathogenic variants in the methionine synthase reductase gene (MTRR). Patients usually exhibit early‐onset bone ma
Externí odkaz:
https://doaj.org/article/75976a26610940dd92291d9485f6970b
Autor:
Dema Alset, Elena Viktorovna Butenko, Inna Olegovna Pokudina, Tatiana Pavlovna Shkurat, Ekaterina Andreevna Zabanova, Natalia Borisovna Kuznetsova
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 24, Iss 1, Pp 1-10 (2023)
Abstract Background Fetal growth restriction (FGR) is one of the main syndromes causing fetal morbidity and mortality. It was known to be associated with different factors including maternal, fetal, and environmental. However, the effect of genetic f
Externí odkaz:
https://doaj.org/article/aaba1f19bdf2477bab91df1a8e4c50d4
Autor:
Alves Antunes, Lívia Azeredo1,2,3,4 liviaazeredo@gmail.com, Cabral Machado, Claudio Manoel2, Kuntz Couto, Ana Carolina2, Lopes, Ludiana Barbosa4, de Sena, Fernanda Cunha1, Abreu, Fernanda Volpe1, Fraga, Renato Silva1,3, Küchler, Erika Calvano5, Antunes, Leonardo Santos1,3,4, Antunes, Lívia Azeredo Alves1 (AUTHOR), Machado, Claudio Manoel Cabral (AUTHOR), Couto, Ana Carolina Kuntz (AUTHOR), Sena, Fernanda Cunha (AUTHOR)
Publikováno v:
Caries Research. Mar2017, Vol. 51 Issue 1, p102-108. 7p. 4 Charts.
Autor:
Lyazzat Kaldygulova, Sauran Yerdessov, Talshyn Ukybassova, Yevgeniy Kim, Dinmukhamed Ayaganov, Andrey Gaiday
Publikováno v:
Biology, Vol 13, Iss 9, p 648 (2024)
Introduction: Preeclampsia is a severe multifactorial complication of pregnancy. Studies found associations between folate metabolism genes’ polymorphisms and preeclampsia. However, investigations in this field are limited among Asian populations.
Externí odkaz:
https://doaj.org/article/8d3d47203d944fcca49caf5be0022e52
Autor:
Asim, Ambreen1 ambreenasimsiddiqui@gmail.com, Agarwal, Sarita1 saritasgpgi@gmail.com, Panigrahi, Inusha2 inupan@yahoo.com
Publikováno v:
Egyptian Journal of Medical Human Genetics. Jan2017, Vol. 18 Issue 1, p61-66. 6p.
Autor:
Xueyuan Zhi1, Boyi Yang2, Shujun Fan1, Yanxun Wang3, Jian Wei4, Quanmei Zheng1, Guifan Sun1 gfsun@cmu.edu.cn
Publikováno v:
Lipids in Health & Disease. 10/28/2016, Vol. 15, p1-9. 9p. 3 Charts.
Publikováno v:
Egyptian Journal of Medical Human Genetics. Apr2016, Vol. 17 Issue 2, p217-221. 5p.
Autor:
Shu-Jun Fan1 fanfan0721ykl@163.com, Bo-Yi Yang1 boyiyangcmu@163.com, Xue-Yuan Zhi1 zhixy90smile@126.com, Miao He1 hemiao.cmu@gmail.com, Da Wang1 472594283@163.com, Yan-Xun Wang2 13817895706@163.com, Yi-Nuo Wang2 wangyanxun@genechina.com, Jian Wei3 weijiantianjin@163.com, Quan-Mei Zheng1 qmzheng@mail.cmu.edu.cn, Gui-Fan Sun1 sungf@mail.cmu.edu.cn
Publikováno v:
International Journal of Molecular Sciences. 2015, Vol. 16 Issue 6, p11849-S8. 23p. 1 Color Photograph, 4 Black and White Photographs, 10 Charts, 2 Graphs.