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The New England Journal of Medicine|March 27, 1980
Successful bone-marrow transplantation for infantile malignant osteopetrosisP F Coccia, W Krivit, J Cervenka, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 2, 2007
Novel mouse model of autosomal semidominant adult hypophosphatasia has a splice site mutation in the tissue nonspecific alkaline phosphatase gene Akp2Tertius A Hough, Monika Polewski, Kristen Johnson, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 10, 1998
An integrated genetic linkage map of the laboratory ratD M Brown, T C Matise, G Koike, et al.
Molecular Therapy. Methods & Clinical Development|August 29, 2022
AAV-mediated rescue of Eps8 expression in vivo restores hair-cell function in a mouse model of recessive deafnessJing-Yi Jeng, Adam J Carlton, Richard J Goodyear, et al.
Phytomedicine : International Journal of Phytotherapy and Phytopharmacology|December 1, 2012
Effect of tannins on screening of plant extracts for enzyme inhibitory activity and techniques for their removalM E Wall, M C Wani, D M Brown, et al.
Human Genetics|January 22, 2005
Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient populationXiao Mei Ouyang, Denise Yan, Li Lin Du, et al.
Human Molecular Genetics|June 28, 2013
IGF-1 receptor antagonism inhibits autophagyMaurizio Renna, Carla F Bento, Angeleen Fleming, et al.
Nucleic Acids Research|October 27, 2009
MouseBook: an integrated portal of mouse resourcesAndrew Blake, Karen Pickford, Simon Greenaway, et al.
The American Journal of Pathology|May 22, 2016
Mouse Models of NMNAT1-Leber Congenital Amaurosis (LCA9) Recapitulate Key Features of the Human DiseaseScott H Greenwald, Jeremy R Charette, Magdalena Staniszewska, et al.
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