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Disease Models & Mechanisms|September 29, 2020
A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in miceZakia Abdelhamed, Marshall Lukacs, Sandra Cindric, et al.
Developmental Biology|March 5, 2013
Aberrant Wnt signalling and cellular over-proliferation in a novel mouse model of Meckel-Gruber syndromeGabrielle Wheway, Zakia Abdelhamed, Subaashini Natarajan, et al.
Plos Genetics|November 16, 2019
Gpr63 is a modifier of microcephaly in Ttc21b mouse mutantsJohn Snedeker, William J Gibbons, David F Paulding, et al.
Plos Genetics|August 7, 2019
Differential requirements of tubulin genes in mammalian forebrain developmentElizabeth Bittermann, Zakia Abdelhamed, Ryan P Liegel, et al.
Development (Cambridge, England)|January 11, 2018
A mutation in Ccdc39 causes neonatal hydrocephalus with abnormal motile cilia development in miceZakia Abdelhamed, Shawn M Vuong, Lauren Hill, et al.
Human Molecular Genetics|November 29, 2011
A meckelin-filamin A interaction mediates ciliogenesisMatthew Adams, Roslyn J Simms, Zakia Abdelhamed, et al.
The Journal of Thoracic and Cardiovascular Surgery|May 10, 2023
Exogenous nitric oxide delivery protects against cardiopulmonary bypass-associated acute kidney injury: Histologic and serologic evidence from an ovine modelJason W Greenberg, Spencer Hogue, Muhammad Aanish Raees, et al.
American Journal of Human Genetics|May 19, 2015
Biallelic mutations in the autophagy regulator DRAM2 cause retinal dystrophy with early macular involvementMohammed E El-Asrag, Panagiotis I Sergouniotis, Martin McKibbin, et al.
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