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HASSAN BAZZI, DO
DO
Family Medicine Physician
NPI: 1366939951IndividualAccepts Medicare
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
5101025688(MI)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
MICHIGAN STATE UNIVERSITY COLLEGE OF OSTEOPATHIC MEDICINE
Class of 2021
Research & Publications (20)
Synthesis and spectroscopic studies of the charge transfer complexes of 2- and 3-aminopyridine.
PMID 19574089·Spectrochim Acta A Mol Biomol Spectrosc·2009
8-other
Dynamic expression of Syndecan-1 during hair follicle morphogenesis.
PMID 19427408·Gene Expr Patterns·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
Synthesis, spectroscopic and thermal investigations of solid charge-transfer complexes of 1,4,7-trimethyl-1,4,7-triazacyclononane and the acceptors iodine, TCNE, TCNQ and chloranil.
PMID 18691934·Spectrochim Acta A Mol Biomol Spectrosc·2008
8-other
Smad4-dependent desmoglein-4 expression contributes to hair follicle integrity.
PMID 18692037·Dev Biol·2008
7-preclinical
Mutations in R-spondin 4 (RSPO4) underlie inherited anonychia.
PMID 17805348·J Invest Dermatol·2008
5-case
Dynamic expression of the zinc-finger transcription factor Trps1 during hair follicle morphogenesis and cycling.
PMID 18054290·Gene Expr Patterns·2008
7-preclinical
Transcriptional profiling of developing mouse epidermis reveals novel patterns of coordinated gene expression.
PMID 17330888·Dev Dyn·2007
7-preclinical
Broken hearts, woolly hair, and tattered skin: when desmosomal adhesion goes awry.
PMID 17951043·Curr Opin Cell Biol·2007
6-review
The Wnt inhibitor, Dickkopf 4, is induced by canonical Wnt signaling during ectodermal appendage morphogenesis.
PMID 17397822·Dev Biol·2007
4-observational
Localized autosomal recessive hypotrichosis due to a frameshift mutation in the desmoglein 4 gene exhibits extensive phenotypic variability within a Pakistani family.
PMID 17392831·J Invest Dermatol·2007
5-case
Mutations in the desmoglein 4 gene underlie localized autosomal recessive hypotrichosis with monilethrix hairs and congenital scalp erosions.
PMID 16543896·J Invest Dermatol·2006
5-case
Desmoglein 4 is expressed in highly differentiated keratinocytes and trichocytes in human epidermis and hair follicle.
PMID 16533311·Differentiation·2006
8-other
Delineation of diversified desmoglein distribution in stratified squamous epithelia: implications in diseases.
PMID 16433681·Exp Dermatol·2006
7-preclinical
Desmoglein 4 mutations underlie localized autosomal recessive hypotrichosis in humans, mice, and rats.
PMID 16382669·J Investig Dermatol Symp Proc·2005
7-preclinical
A missense mutation in the cadherin interaction site of the desmoglein 4 gene underlies localized autosomal recessive hypotrichosis.
PMID 16297213·J Invest Dermatol·2005
5-case
Regulation of ultraviolet B radiation-mediated activation of AP1 signaling by retinoids in primary keratinocytes.
PMID 15733037·Radiat Res·2005
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
- 8209 ALLEN RD
ALLEN PARK, MI 48101 - Phone
- (313) 675-0182
Quick Facts
- NPI
- 1366939951
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 5
- Publications
- 20
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