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Development (Cambridge, England)|July 12, 2012
fras1 shapes endodermal pouch 1 and stabilizes zebrafish pharyngeal skeletal developmentJared Coffin Talbot, Macie B Walker, Thomas J Carney, et al.
The Journal of Physical Chemistry Letters|October 30, 2015
Electrode-electrolyte interface in Li-ion batteries: current understanding and new insightsMagali Gauthier, Thomas J Carney, Alexis Grimaud, et al.
Plos Genetics|April 27, 2010
Genetic analysis of fin development in zebrafish identifies furin and hemicentin1 as potential novel fraser syndrome disease genesThomas J Carney, Natália Martins Feitosa, Carmen Sonntag, et al.
Plos Genetics|March 29, 2008
Leukocyte tyrosine kinase functions in pigment cell developmentSusana S Lopes, Xueyan Yang, Jeanette Müller, et al.
American Journal of Medical Genetics. Part A|February 25, 2022
Huriez syndrome: Additional pathogenic variants supporting allelism to SMARCAD syndromeAbigail Y T Loh, Sanja Špoljar, Granville Y W Neo, et al.
Nature Communications|March 6, 2023
Zebrafish pigment cells develop directly from persistent highly multipotent progenitorsTatiana Subkhankulova, Karen Camargo Sosa, Leonid A Uroshlev, et al.
American Journal of Human Genetics|April 10, 2012
Attenuated BMP1 function compromises osteogenesis, leading to bone fragility in humans and zebrafishP V Asharani, Katharina Keupp, Oliver Semler, et al.
Human Molecular Genetics|May 10, 2018
Functional analysis of a hypomorphic allele shows that MMP14 catalytic activity is the prime determinant of the Winchester syndrome phenotypeIvo J H M de Vos, Evelyn Yaqiong Tao, Sheena Li Ming Ong, et al.
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