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Human Genetics|December 20, 2021
Challenges in the diagnosis of neurofibromatosis type 1 (NF1) in young children facilitated by means of revised diagnostic criteria including genetic testing for pathogenic NF1 gene variantsHildegard Kehrer-Sawatzki, David N CooperHuman Genomics|February 8, 2011
Exploring the potential relevance of human-specific genes to complex diseaseDavid N Cooper, Hildegard Kehrer-SawatzkiHuman Mutation|October 7, 2006
Understanding the recent evolution of the human genome: insights from human-chimpanzee genome comparisonsHildegard Kehrer-Sawatzki, David N CooperFamilial Cancer|August 12, 2025
SMARCB1-related schwannomatosis and other SMARCB1-associated phenotypes: clinical spectrum and molecular pathogenesisHildegard Kehrer-Sawatzki, David N CooperHuman Genetics|October 27, 2006
Structural divergence between the human and chimpanzee genomesHildegard Kehrer-Sawatzki, David N CooperHuman Genetics|December 30, 2008
Air pollution and mutations in the germline: are humans at risk?Christopher M Somers, David N CooperHuman Genetics|December 6, 2013
The emergence of the mitochondrial genome as a partial regulator of nuclear function is providing new insights into the genetic mechanisms underlying age-related complex diseaseMartin P Horan, David N CooperChromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|February 23, 2008
Molecular mechanisms of chromosomal rearrangement during primate evolutionHildegard Kehrer-Sawatzki, David N CooperHuman Molecular Genetics|May 3, 2006
Influence of human genome polymorphism on gene expressionTomi Pastinen, Bing Ge, Thomas J HudsonPhysiological Genomics|January 11, 2007
1alpha,25-dihydroxy-vitamin D3 stimulation of bronchial smooth muscle cells induces autocrine, contractility, and remodeling processesYohan Bossé, Karim Maghni, Thomas J HudsonPageof 57