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ARTHUR CHRISTIANO, MD
MD
Urology Physician
NPI: 1780668483IndividualAccepts Medicare
Specialties, Licenses & Credentials
Urology PhysicianPrimary
Urology
Code: 208800000X
MA070444(NJ)
CMS Specialties
PrimaryUROLOGY
Education
OTHER
Class of 1994
Research & Publications (20)
Founder mutations in the lipase h gene in families with autosomal recessive woolly hair/hypotrichosis.
PMID 19262606·J Invest Dermatol·2009
8-other
Identification of mutations in the EDA and EDAR genes in Pakistani families with hypohidrotic ectodermal dysplasia.
PMID 19438931·Clin Genet·2009
8-other
Mutations in the lipase H gene underlie autosomal recessive woolly hair/hypotrichosis.
PMID 18830268·J Invest Dermatol·2009
8-other
Autosomal recessive woolly hair with hypotrichosis caused by a novel homozygous mutation in the P2RY5 gene.
PMID 18803659·Exp Dermatol·2009
5-case
The effect of inbreeding on the distribution of compound heterozygotes: a lesson from Lipase H mutations in autosomal recessive woolly hair/hypotrichosis.
PMID 19365138·Hum Hered·2009
8-other
Mutations in the desmoglein 1 gene in five Pakistani families with striate palmoplantar keratoderma.
PMID 19157795·J Dermatol Sci·2009
8-other
KGF and EGF signalling block hair follicle induction and promote interfollicular epidermal fate in developing mouse skin.
PMID 19474150·Development·2009
7-preclinical
Amelioration of epidermolysis bullosa by transfer of wild-type bone marrow cells.
PMID 18955559·Blood·2009
7-preclinical
Progressive symmetrical erythrokeratoderma: report of a Turkish family and evaluation for loricrin and connexin gene mutations.
PMID 18462442·Clin Exp Dermatol·2008
5-case
Mutations in the hairless gene underlie APL in three families of Pakistani origin.
PMID 18164595·J Dermatol Sci·2008
8-other
Smad4-dependent desmoglein-4 expression contributes to hair follicle integrity.
PMID 18692037·Dev Biol·2008
7-preclinical
A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice.
PMID 18713754·Hum Mol Genet·2008
7-preclinical
Novel mutation in the human hairless gene once more erroneously diagnosed and treated as 'alopecia areata'.
PMID 18241276·Br J Dermatol·2008
5-case
P-cadherin is a p63 target gene with a crucial role in the developing human limb bud and hair follicle.
PMID 18199584·Development·2008
7-preclinical
FOXN1 homozygous mutation associated with anencephaly and severe neural tube defect in human athymic Nude/SCID fetus.
PMID 18339010·Clin Genet·2008
7-preclinical
Disruption of P2RY5, an orphan G protein-coupled receptor, underlies autosomal recessive woolly hair.
PMID 18297072·Nat Genet·2008
5-case
Genome-wide linkage analysis of an autosomal recessive hypotrichosis identifies a novel P2RY5 mutation.
PMID 18692127·Genomics·2008
7-preclinical
Molecular dynamics of host-guest complexes of small gas molecules with calix[4]arenes.
PMID 18593133·J Phys Chem A·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
- 595 SHREWSBURY AVE
SHREWSBURY, NJ 07702 - Phone
- (732) 741-5923
Quick Facts
- NPI
- 1780668483
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 32
- Publications
- 20
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