Výsledky vyhledávání - "Sai Lao"

Akademický článek

Choline dehydrogenase polymorphism rs12676 is a functional variation and is associated with changes in human sperm cell function.

Autor: Amy R Johnson, Sai Lao, Tongwen Wang, Joseph A Galanko, Steven H Zeisel

Publikováno v: PLoS ONE, Vol 7, Iss 4, p e36047 (2012)

Approximately 15% of couples are affected by infertility and up to half of these cases arise from male factor infertility. Unidentified genetic aberrations such as chromosomal deletions, translocations and single nucleotide polymorphisms (SNPs) may b

Externí odkaz: https://doaj.org/article/edd56c4af4604b11863b4d55d82fb711

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Akademický článek

Choline Dehydrogenase Polymorphism rs12676 Is a Functional Variation and Is Associated with Changes in Human Sperm Cell Function.

Autor: Johnson, Amy R.¹, Sai Lao¹, Tongwen Wang^1,2, Galanko, Joseph A.³, Zeisel, Steven H.^1,2 stevenzeisel@unc.edu

Publikováno v: PLoS ONE. Apr2012, Vol. 7 Issue 4, p1-12. 12p.

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Effect of Chdh deletion on mouse fetal neurogenesis and apoptosis

Autor: Ya‐Wen Teng, Mihai G. Mehedint, Sai Lao, Steven H. Zeisel, Shucha Zhang, Amy R. Johnson

Publikováno v: The FASEB Journal. 27

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::65f02f5b6fa7bcfbd5a64f780d994ed1
https://doi.org/10.1096/fasebj.27.1_supplement.1058.7

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Choline dehydrogenase polymorphism rs12676 is a functional variation associated with changes in human sperm cell function

Autor: Tongwen Wang, Sai Lao, Steven H. Zeisel, Joseph A. Galanko, Amy R. Johnson

Publikováno v: The FASEB Journal. 26

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::88736bedc46e123ddda0ecfc19c52ed0
https://doi.org/10.1096/fasebj.26.1_supplement.126.7

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Choline Dehydrogenase Polymorphism rs12676 Is a Functional Variation and Is Associated with Changes in Human Sperm Cell Function

Autor: Sai Lao, Amy R. Johnson, Joseph A. Galanko, Tongwen Wang, Steven H. Zeisel

Publikováno v: PLoS ONE
PLoS ONE, Vol 7, Iss 4, p e36047 (2012)

Approximately 15% of couples are affected by infertility and up to half of these cases arise from male factor infertility. Unidentified genetic aberrations such as chromosomal deletions, translocations and single nucleotide polymorphisms (SNPs) may b

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2493aca04e3785cbd5ad54a2fda95b22

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