Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Chun-Wei Allen Feng"'
Autor:
Uda Y. Ho, Chun-Wei Allen Feng, Yvonne Y. Yeap, Amanda L. Bain, Zhe Wei, Belal Shohayeb, Melissa E. Reichelt, Hayden Homer, Kum Kum Khanna, Josephine Bowles, Dominic C. H. Ng
Publikováno v:
Communications Biology, Vol 4, Iss 1, Pp 1-14 (2021)
Uda Ho et al find that loss of centriolar scaffold protein WDR62 in mouse testis leads to defects in spermatogenesis. They find that WDR62 deficiency leads to centriole underduplication in spermatocytes and delayed manchette removal in spermatids due
Externí odkaz:
https://doaj.org/article/5fa87d30eabf4504b9c5fb5bd757b344
Autor:
Guillaume Burnet, Chun‐Wei Allen Feng, Ka Man Fiona Cheung, Josephine Bowles, Cassy M. Spiller
Publikováno v:
genesis. 61
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d253f63ae1ca5c0d41e332a7f6a0d4d8
https://doi.org/10.1002/dvg.23511
https://doi.org/10.1002/dvg.23511
Autor:
Belal Shohayeb, Zhe Wei, Kum Kum Khanna, Amanda L. Bain, Josephine Bowles, Uda Ho, Dominic C.H. Ng, Yvonne Y C Yeap, Chun-Wei Allen Feng, Melissa E. Reichelt, Hayden Homer
Publikováno v:
Communications Biology
Communications Biology, Vol 4, Iss 1, Pp 1-14 (2021)
Communications Biology, Vol 4, Iss 1, Pp 1-14 (2021)
WDR62 is a scaffold protein involved in centriole duplication and spindle assembly during mitosis. Mutations in WDR62 can cause primary microcephaly and premature ovarian insufficiency. We have generated a genetrap mouse model deficient in WDR62 and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3f9ba191333efb8904c2efa91256f19
https://pubmed.ncbi.nlm.nih.gov/34059773
https://pubmed.ncbi.nlm.nih.gov/34059773
Autor:
Peter Koopman, Donna Jo Merriner, Chun Wei Allen Feng, Moira K O'Bryan, Cassy M. Spiller, Josephine Bowles
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-12 (2017)
Scientific Reports
Scientific Reports
Male infertility is a major and growing problem and, in most cases, the specific root cause is unknown. Here we show that the transcription factor SOX30 plays a critical role in mouse spermatogenesis. Sox30-null mice are healthy and females are ferti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a96453b573c1623353dfe04b2a1297e
http://link.springer.com/article/10.1038/s41598-017-17854-5
http://link.springer.com/article/10.1038/s41598-017-17854-5