Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Matthew B. Lucas"'
Autor:
Anne Griffin, Tammy Benteau, Sumit K. Agrawal, Cindy Penney, Christopher N. Rowley, Courtney MacDonald, Valerie Booth, Lorne S. Parnes, Ahmed A. Mostafa, Susan J Moore, Terry-Lynn Young, Lisbeth Tranebjærg, Tony Batten, Darren D. O’Rielly, Matthew B. Lucas, Curtis R. French, Leichelle A. Little, Nanna Dahl Rendtorff, Jim Houston, Pingzhao Hu, Justin A. Pater, Danielle French, Susan G. Stanton, Dante Galutira, Kathy Hodgkinson, Nelly Abdelfatah, Lance P. Doucette, Jessica E. Besaw
Publikováno v:
Abdelfatah, N, Mostafa, A A, French, C R, Doucette, L P, Penney, C, Lucas, M B, Griffin, A, Booth, V, Rowley, C, Besaw, J E, Tranebjærg, L, Rendtorff, N D, Hodgkinson, K A, Little, L A, Agrawal, S, Parnes, L, Batten, T, Moore, S, Hu, P, Pater, J A, Houston, J, Galutira, D, Benteau, T, MacDonald, C, French, D, O’Rielly, D D, Stanton, S G & Young, T L 2022, ' A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) gene ', Human Genetics, vol. 141, pp. 965–979 . https://doi.org/10.1007/s00439-021-02381-1
Otosclerosis is a bone disorder of the otic capsule and common form of late-onset hearing impairment. Considered a complex disease, little is known about its pathogenesis. Over the past 20 years, ten autosomal dominant loci (OTSC1-10) have been mappe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bf6cfb0bb7f5d5a0bba921775b726b4
https://pubmed.ncbi.nlm.nih.gov/34633540
https://pubmed.ncbi.nlm.nih.gov/34633540
Tumors and cancers of the gastrointestinal tract and pancreas are commonly derived from precursor lesions so that understanding the physiological, cellular, and molecular mechanisms underlying the pathogenesis of precursor lesions is critical for the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0af9befa0b9bd9c4ef0b824a39d0ac1b
https://europepmc.org/articles/PMC4644877/
https://europepmc.org/articles/PMC4644877/
Publikováno v:
Journal of Molecular and Genetic Medicine.
Mahvash disease is a novel pancreatic neuroendocrine tumor syndrome caused by inactivating glucagon receptor mutations. Its discovery was triggered by comparison of a patient with pancreatic neuroendocrine tumors, pancreatic α cell hyperplasia, extr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::543f416eb413648e37bf9c6767db6e17
https://doi.org/10.4172/1747-0862.1000084
https://doi.org/10.4172/1747-0862.1000084