Showing results (21-30 of 63) with videos related to

Sort By:
Pageof 7
Genetics|February 16, 2011
Modifier genes for mouse phosphatidylinositol transfer protein α (vibrator) that bypass juvenile lethalityDorothy Concepcion, Frank Johannes, Yuan Hung Lo, et al.
Plos Genetics|April 4, 2015
Nxf1 natural variant E610G is a semi-dominant suppressor of IAP-induced RNA processing defectsDorothy Concepcion, Kevin D Ross, Kasey R Hutt, et al.
Kidney International|September 17, 2005
Analyses of coding region polymorphisms in apical and basolateral human organic anion transporter (OAT) genes [OAT1 (NKT), OAT2, OAT3, OAT4, URAT (RST)]Gang Xu, Vibha Bhatnagar, Gen Wen, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 8, 2006
Zfp423 controls proliferation and differentiation of neural precursors in cerebellar vermis formationWendy A Alcaraz, David A Gold, Eric Raponi, et al.
Human Molecular Genetics|July 7, 2011
Modifier genes and non-genetic factors reshape anatomical deficits in Zfp423-deficient miceWendy A Alcaraz, Edward Chen, Phoebe Valdes, et al.
Journal of Human Genetics|May 2, 2006
Analyses of 5' regulatory region polymorphisms in human SLC22A6 (OAT1) and SLC22A8 (OAT3)Vibha Bhatnagar, Gang Xu, Bruce A Hamilton, et al.
Molecular Pharmacology|August 25, 2004
The catecholamine release-inhibitory "catestatin" fragment of chromogranin a: naturally occurring human variants with different potencies for multiple chromaffin cell nicotinic cholinergic responsesSushil K Mahata, Manjula Mahata, Gen Wen, et al.
Developmental Biology|January 7, 2018
TBR2 antagonizes retinoic acid dependent neuronal differentiation by repressing Zfp423 during corticogenesisLuca Massimino, Lisbeth Flores-Garcia, Bruno Di Stefano, et al.
Plos Genetics|October 15, 2025
Tulp3 quantitative alleles titrate requirements for viability, brain development, and kidney homeostasis but do not suppress Zfp423 mutations in miceCorinne A McCoy, Dorothy Concepcion, Mark G Mezody, et al.
Biorxiv : the Preprint Server for Biology|May 13, 2026
<i>Mysm1</i> mutations in <i>meander tail</i> mice cause anterior-selective cerebellum malformationBruce A Hamilton, Dorothy Concepcion, Max Chang, et al.
Pageof 7