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WILLIAM MCLEAN, MD
MD
Student in an Organized Health Care Education/Training Program
NPI: 1598516783Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
Keratin K6c mutations cause focal palmoplantar keratoderma.
PMID 19609311·J Invest Dermatol·2010
8-other
Distribution of the Na,K-ATPase alpha subunit in the rat spiral ganglion and organ of corti.
PMID 19082858·J Assoc Res Otolaryngol·2009
7-preclinical
Prevalent and rare mutations in the gene encoding filaggrin in Japanese patients with ichthyosis vulgaris and atopic dermatitis.
PMID 19037238·J Invest Dermatol·2009
5-case
Carrier status for the common R501X and 2282del4 filaggrin mutations is not associated with hearing phenotypes in 5,377 children from the ALSPAC cohort.
PMID 19492053·PLoS One·2009
8-other
Copy-number mutations on chromosome 17q24.2-q24.3 in congenital generalized hypertrichosis terminalis with or without gingival hyperplasia.
PMID 19463983·Am J Hum Genet·2009
8-other
FLG mutation p.Lys4021X in the C-terminal imperfect filaggrin repeat in Japanese patients with atopic eczema.
PMID 19663875·Br J Dermatol·2009
8-other
Analysis of Taiwanese ichthyosis vulgaris families further demonstrates differences in FLG mutations between European and Asian populations.
PMID 19416262·Br J Dermatol·2009
8-other
Filaggrin in the frontline: role in skin barrier function and disease.
PMID 19386895·J Cell Sci·2009
7-preclinical
A homozygous frameshift mutation in the mouse Flg gene facilitates enhanced percutaneous allergen priming.
PMID 19349982·Nat Genet·2009
7-preclinical
Eczema genetics: current state of knowledge and future goals.
PMID 19209157·J Invest Dermatol·2009
6-review
Ichthyosis vulgaris: novel FLG mutations in the German population and high presence of CD1a+ cells in the epidermis of the atopic subgroup.
PMID 19183181·Br J Dermatol·2009
8-other
Keratin 7 promoter selectively targets transgene expression to normal and neoplastic pancreatic ductal cells in vitro and in vivo.
PMID 19124560·FASEB J·2009
7-preclinical
Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis.
PMID 19122663·Nat Genet·2009
5-case
Filaggrin haploinsufficiency is highly penetrant and is associated with increased severity of eczema: further delineation of the skin phenotype in a prospective epidemiological study of 792 school children.
PMID 19681860·Br J Dermatol·2009
8-other
Mutation in DSG1 causing autosomal dominant striate palmoplantar keratoderma.
PMID 19558595·Br J Dermatol·2009
5-case
Heterozygous null alleles in filaggrin contribute to clinical dry skin in young adults and the elderly.
PMID 18987673·J Invest Dermatol·2009
8-other
Filaggrin loss-of-function variants are associated with atopic comorbidity in pediatric inflammatory bowel disease.
PMID 19408338·Inflamm Bowel Dis·2009
4-observational
Clinical severity correlates with impaired barrier in filaggrin-related eczema.
PMID 18818676·J Invest Dermatol·2009
7-preclinical
Association of skin barrier genes within the PSORS4 locus is enriched in Singaporean Chinese with early-onset psoriasis.
PMID 18787534·J Invest Dermatol·2009
8-other
Steatocystoma multiplex, oligodontia and partial persistent primary dentition associated with a novel keratin 17 mutation.
PMID 19659471·Br J Dermatol·2009
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 3500 GASTON AVE
DALLAS, TX 75246 - Phone
- (214) 820-0111
Quick Facts
- NPI
- 1598516783
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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