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Journal of Medicinal Chemistry|November 17, 2012
Free-Wilson and structural approaches to co-optimizing human and rodent isoform potency for 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) inhibitorsFrederick W Goldberg, Andrew G Leach, James S Scott, et al.
Genomics, Proteomics & Bioinformatics|October 2, 2022
Newfound Coding Potential of Transcripts Unveils Missing Members of Human Protein CommunitiesSébastien Leblanc, Marie A Brunet, Jean-François Jacques, et al.
BMC Medical Genetics|February 19, 2020
Two monogenic disorders masquerading as one: severe congenital neutropenia with monocytosis and non-syndromic sensorineural hearing lossParvathy Venugopal, Lucia Gagliardi, Cecily Forsyth, et al.
European Journal of Immunology|August 15, 2000
RNA and protein expression of the murine autoimmune regulator gene (Aire) in normal, RelB-deficient and in NOD mouseM Heino, P Peterson, N Sillanpää, et al.
Human Genetics|December 18, 1998
A common mutation in Sardinian autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patientsM C Rosatelli, A Meloni, A Meloni, et al.
Nature Genetics|April 24, 2007
Modifiers of epigenetic reprogramming show paternal effects in the mouseSuyinn Chong, Nicola Vickaryous, Alyson Ashe, et al.
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