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YASMINA BOYD, M.D
M.D
Emergency Medicine Physician
NPI: 1619152253Individual
Specialties, Licenses & Credentials
Emergency Medicine PhysicianPrimary
Emergency Medicine
Code: 207P00000X
20A7941(CA)
Research & Publications (15)
A phenotype map of the mouse X chromosome: models for human X-linked disease.
PMID 10720569·Genome Res·2000
4-observational
Host genes affect intestinal colonisation of newly hatched chickens by Campylobacter jejuni.
PMID 15900496·Immunogenetics·2005
4-observational
Identification and characterization of a functional, alternatively spliced Toll-like receptor 7 (TLR7) and genomic disruption of TLR8 in chickens.
PMID 15804288·Immunology·2005
4-observational
Identification and functional characterization of chicken toll-like receptor 5 reveals a fundamental role in the biology of infection with Salmonella enterica serovar typhimurium.
PMID 15784580·Infect Immun·2005
7-preclinical
A dominant mutation within the DNA-binding domain of the bZIP transcription factor Maf causes murine cataract and results in selective alteration in DNA binding.
PMID 12620964·Hum Mol Genet·2003
7-preclinical
Orthologs of seven genes (AKT1, CDC42BPB, DIO3, EIF5, JAG2, KLC, NDUFB1) from human chromosome 14q32 map to distal chicken chromosome 5.
PMID 11889562·Mamm Genome·2002
7-preclinical
Chromosomal assignments of mammalian genes with an acute inflammation-regulated expression in liver.
PMID 11797096·Immunogenetics·2001
7-preclinical
The genes encoding E-selectin (SELE) and lymphotactin (SCYC1) lie on separate chicken chromosomes although they are closely linked in human and mouse.
PMID 11685458·Immunogenetics·2001
7-preclinical
Intragenic deletions at Atp7a in mouse models for Menkes disease.
PMID 11386751·Genomics·2001
7-preclinical
Transgenic rescue of the tattered phenotype by using a BAC encoding Ebp.
PMID 11309666·Mamm Genome·2001
7-preclinical
Mapping of the chicken and mouse genes for toll-like receptor 2 (TLR2) to an evolutionarily conserved chromosomal segment.
PMID 11220633·Immunogenetics·2001
7-preclinical
Further genetic analysis of two autosomal dominant mouse eye defects, Ccw and Pax6(coop).
PMID 11062307·Mol Vis·2000
7-preclinical
Positioning of five genes (CASK, ARX, SAT, IMAGE cDNAs 248928 and 253949) from the human X chromosome short arm with respect to evolutionary breakpoints on the mouse X chromosome.
PMID 10920247·Mamm Genome·2000
4-observational
The sex-linked fidget mutation abolishes Brn4/Pou3f4 gene expression in the embryonic inner ear.
PMID 10587581·Hum Mol Genet·2000
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2101 N WATERMAN AVE
SAN BERNARDINO, CA 92404 - Phone
- (909) 881-4357
Quick Facts
- NPI
- 1619152253
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 15
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