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Developmental Biology|November 27, 2024
A conditional smoothened (smo) allele on an inbred C57BL/6J genetic background has a hypomorphic smo mutant phenotypeScott Houghtaling, Sean K Gombart, Tzu-Hua Ho, et al.
Medrxiv : the Preprint Server for Health Sciences|January 27, 2025
NUBP2 deficiency disrupts the centrosome-check point in the brain and causes primary microcephalyRebekah Rushforth, Hanan E Shamseldin, Nicole Costantino, et al.
Journal of Neurogenetics|November 8, 2002
A novel mutation in the gene encoding noggin is not causative in human neural tube defectsKim A Bauer, Timothy M George, David S Enterline, et al.
Human Molecular Genetics|December 17, 2009
Prdm16 is required for normal palatogenesis in miceBryan C Bjork, Annick Turbe-Doan, Mary Prysak, et al.
BMC Genomics|November 11, 2015
Variant mapping and mutation discovery in inbred mice using next-generation sequencingJabier Gallego-Llamas, Andrew E Timms, Krista A Geister, et al.
Journal of the American Society of Nephrology : JASN|February 1, 2008
Nek8 regulates the expression and localization of polycystin-1 and polycystin-2Eisei Sohara, Ying Luo, Jingjing Zhang, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|April 24, 2009
An N-ethyl-N-nitrosourea mutagenesis recessive screen identifies two candidate regions for murine cardiomyopathy that map to chromosomes 1 and 15Liliana Fernandez, Douglas A Marchuk, Jennifer L Moran, et al.
Journal of Developmental Biology|September 23, 2020
Reelin Mediates Hippocampal Cajal-Retzius Cell Positioning and Infrapyramidal Blade MorphogenesisSeungshin Ha, Prem P Tripathi, Ray A Daza, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 27, 2017
C-Terminal Region Truncation of RELN Disrupts an Interaction with VLDLR, Causing Abnormal Development of the Cerebral Cortex and HippocampusSeungshin Ha, Prem P Tripathi, Anca B Mihalas, et al.
American Journal of Medical Genetics. Part A|September 27, 2021
Robin sequence without cleft palate: Genetic diagnoses and management implicationsK Nicole Weaver, Bonnie R Sullivan, Stephanie A Balow, et al.
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