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BMC Proceedings|December 19, 2014
Mapping genes with longitudinal phenotypes via Bayesian posterior probabilitiesAnthony Musolf, Alejandro Q Nato, Douglas Londono, et al.
International Journal of Molecular Sciences|September 9, 2022
Comorbidity of Novel CRHR2 Gene Variants in Type 2 Diabetes and DepressionMutaz Amin, Jurg Ott, Derek Gordon, et al.
Nature Genetics|February 26, 2008
Disruption of P2RY5, an orphan G protein-coupled receptor, underlies autosomal recessive woolly hairYutaka Shimomura, Muhammad Wajid, Yoshiyuki Ishii, et al.
Acta Crystallographica. Section E, Structure Reports Online|December 27, 2011
N'-(4-Meth-oxy-benzyl-idene)-4-methyl-benzohydrazideZeng-Xin Liu
Acta Crystallographica. Section E, Structure Reports Online|December 27, 2011
N'-(2-Hy-droxy-benzyl-idene)-3-methyl-benzohydrazideZeng-Xin Liu
Journal of Molecular Medicine (Berlin, Germany)|December 16, 2004
Identification of a recurrent mutation in GALNT3 demonstrates that hyperostosis-hyperphosphatemia syndrome and familial tumoral calcinosis are allelic disordersYaacov Frishberg, Orit Topaz, Reuven Bergman, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 25, 2004
Association of the dihydrolipoamide dehydrogenase gene with Alzheimer's disease in an Ashkenazi Jewish populationAbraham M Brown, Derek Gordon, Hsinhwa Lee, et al.
Molecular Carcinogenesis|March 21, 2012
A keratin 15 containing stem cell population from the hair follicle contributes to squamous papilloma development in the mouseShulan Li, Heuijoon Park, Carol S Trempus, et al.
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