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NATHANIEL HAYWARD III MD
MD
Internal Medicine Physician
NPI: 1467862946IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
R7019(TX)
Education
OTHER
Class of 2014
Research & Publications (20)
The association between MC1R genotype and BRAF mutation status in cutaneous melanoma: findings from an Australian population.
PMID 19571821·J Invest Dermatol·2010
8-other
Global expression profiling of sex cord stromal tumors from Men1 heterozygous mice identifies altered TGF-beta signaling, decreased Gata6 and increased Csf1r expression.
PMID 19058182·Int J Cancer·2009
7-preclinical
A first-in-man phase i and pharmacokinetic study on CHR-2797 (Tosedostat), an inhibitor of M1 aminopeptidases, in patients with advanced solid tumors.
PMID 19638462·Clin Cancer Res·2009
3-trial
A sensory neuronal ion channel essential for airway inflammation and hyperreactivity in asthma.
PMID 19458046·Proc Natl Acad Sci U S A·2009
7-preclinical
Genome-wide association study identifies three loci associated with melanoma risk.
PMID 19578364·Nat Genet·2009
8-other
Murine neonatal melanocytes exhibit a heightened proliferative response to ultraviolet radiation and migrate to the epidermal basal layer.
PMID 18633434·J Invest Dermatol·2009
7-preclinical
Identification of candidate tumor suppressor genes inactivated by promoter methylation in melanoma.
PMID 18803327·Genes Chromosomes Cancer·2009
8-other
Polymorphisms in the syntaxin 17 gene are not associated with human cutaneous malignant melanoma.
PMID 19209086·Melanoma Res·2009
4-observational
A population-based study of Australian twins with melanoma suggests a strong genetic contribution to liability.
PMID 19357710·J Invest Dermatol·2009
8-other
H-cadherin expression reduces invasion of malignant melanoma.
PMID 19368692·Pigment Cell Melanoma Res·2009
7-preclinical
Dual loss of Rb1 and Trp53 in melanocytes perturbs melanocyte homeostasis and genetic stability in vitro but does not cause melanoma or pigmentation defects in vivo.
PMID 19243574·Pigment Cell Melanoma Res·2009
7-preclinical
Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi.
PMID 19578365·Nat Genet·2009
4-observational
Strong evidence for a novel schizophrenia risk locus on chromosome 1p31.1 in homogeneous pedigrees from Tamil Nadu, India.
PMID 18829870·Am J Psychiatry·2009
8-other
Mouse pigmentation mutants help identify a uveal melanoma oncogene.
PMID 19140886·Pigment Cell Melanoma Res·2009
7-preclinical
Genome-wide copy number analysis in esophageal adenocarcinoma using high-density single-nucleotide polymorphism arrays.
PMID 18519675·Cancer Res·2008
8-other
Gene expression analysis in absence epilepsy using a monozygotic twin design.
PMID 18435749·Epilepsia·2008
4-observational
Common sequence variants on 20q11.22 confer melanoma susceptibility.
PMID 18488026·Nat Genet·2008
8-other
Variation in bone morphogenetic protein 15 is not associated with spontaneous human dizygotic twinning.
PMID 18614612·Hum Reprod·2008
8-other
Single nucleotide polymorphisms in obesity-related genes and the risk of esophageal cancers.
PMID 18398047·Cancer Epidemiol Biomarkers Prev·2008
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1001 N WALDROP DR STE 602
ARLINGTON, TX 76012 - Phone
- (817) 277-4723
Quick Facts
- NPI
- 1467862946
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 12
- Publications
- 20
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