David J. Bernard

机构：National Human Genome Research Institute · ORCID：0000-0002-0057-9353

发表论文 47 篇 · 总被引 2295 次 · h-index 20

代表论文

• Proliferative Defect and Embryonic Lethality in Mice Homozygous for a Deletion in the p110α Subunit of Phosphoinositide 3-Kinase (1999 · Journal of Biological Chemistry · 被引 454)
• Early embryonic lethality in mice deficient in the p110β catalytic subunit of PI 3-kinase (2002 · Mammalian Genome · 被引 313)
• Targeted Disruption of the Cln3 Gene Provides a Mouse Model for Batten Disease (1999 · Neurobiology of Disease · 被引 208)
• Functional overlap between murine Inpp5b and Ocrl1 may explain why deficiency of the murine ortholog for OCRL1 does not cause Lowe syndrome in mice. (1998 · Journal of Clinical Investigation · 被引 186)
• T cell diversity and TcR repertoires in teleost fish (2010 · Fish & Shellfish Immunology · 被引 118)
• Spectrum of Mutations in the OCRL1Gene in the Lowe Oculocerebrorenal Syndrome (1997 · The American Journal of Human Genetics · 被引 112)