Zobrazeno 1 - 10
of 66
pro vyhledávání: '"GREB1L"'
Autor:
Sara A. Hugentobler, Anna M. Sturrock, Malte Willmes, Tasha Q. Thompson, Rachel C. Johnson, Flora Cordoleani, Natalie J. Stauffer‐Olsen, George Whitman, Mariah H. Meek
Publikováno v:
Evolutionary Applications, Vol 17, Iss 7, Pp n/a-n/a (2024)
Abstract Chinook salmon (Oncorhynchus tshawytscha) display remarkable life history diversity, underpinning their ability to adapt to environmental change. Maintaining life history diversity is vital to the resilience and stability of Chinook salmon m
Externí odkaz:
https://doaj.org/article/656b89c90c3f4512ad97e04433816104
Autor:
Ke Dong, Chenchen Geng, Xiaohong Zhan, Zhi Sun, Qian Pu, Peng Li, Haiyun Song, Guanghui Zhao, Haidong Gao
Publikováno v:
European Journal of Medical Research, Vol 28, Iss 1, Pp 1-13 (2023)
Abstract Background Breast cancer is the most common malignant tumor among women worldwide. GREB1L is a protein-coding gene. Previous studies have shown that GREB1L plays a vital role in lung and gastric adenocarcinoma. Currently, there is no relevan
Externí odkaz:
https://doaj.org/article/f6f38b8c0f9343a2a08aa4aed7866c82
Autor:
Samuel Mawuli Adadey, Elvis Twumasi Aboagye, Kevin Esoh, Anushree Acharya, Thashi Bharadwaj, Nicole S. Lin, Lucas Amenga-Etego, Gordon A. Awandare, Isabelle Schrauwen, Suzanne M. Leal, Ambroise Wonkam
Publikováno v:
BMC Medical Genomics, Vol 15, Iss 1, Pp 1-10 (2022)
Abstract Background Childhood hearing impairment (HI) is genetically heterogeneous with many implicated genes, however, only a few of these genes are reported in African populations. Methods This study used exome and Sanger sequencing to resolve the
Externí odkaz:
https://doaj.org/article/c26c36b2c8bc4f9cbf88d7ad662a1b90
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-9 (2022)
Abstract Background Renal hypodysplasia/aplasia-3 (RHDA3), as the most severe end of the spectrum of congenital anomalies of the kidney and urinary tract, is mainly caused by mutations in GREB1L. However, the mutations in GREB1L identified to date on
Externí odkaz:
https://doaj.org/article/d8515d13be9c49f691ca255c44ce9592
Publikováno v:
Zhongguo quanke yixue, Vol 26, Iss 08, Pp 1028-1030 (2023)
Renal agenesis and hypodysplasia (RAH) are major congenital anomalies of the kidney and urinary tract that often cause chronic kidney disease in children. Genetic factors are closely related to the pathogenesis of RAH. As whole genome sequencing tech
Externí odkaz:
https://doaj.org/article/548a958f165c47f2af7c196b0bdb1d0d
Akademický článek
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Publikováno v:
Ecology and Evolution, Vol 10, Iss 17, Pp 9486-9502 (2020)
Abstract Fish migrations are energetically costly, especially when moving between freshwater and saltwater, but are a viable strategy for Pacific salmon and trout (Oncorhynchus spp.) due to the advantageous resources available at various life stages.
Externí odkaz:
https://doaj.org/article/7151064f2b164a29b065cec2f3ac2cb6
Akademický článek
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Publikováno v:
BMC Evolutionary Biology, Vol 18, Iss 1, Pp 1-11 (2018)
Abstract Background Disparity in the timing of biological events occurs across a variety of systems, yet the understanding of genetic basis underlying diverse phenologies remains limited. Variation in maturation timing occurs in steelhead trout, whic
Externí odkaz:
https://doaj.org/article/55d65ed19c144f2e80427eecec5fc5e5