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MUHAMMED AYUB, M.D.
M.D.
Internal Medicine Physician
NPI: 1710941836IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
MA62351(NJ)
CMS Specialties
PrimaryINTERNAL MEDICINE
Education
OTHER
Class of 1989
Research & Publications (20)
Oligodontia is caused by mutation in LTBP3, the gene encoding latent TGF-beta binding protein 3.
PMID 19344874·Am J Hum Genet·2009
8-other
Mutations in the P2RY5 gene underlie autosomal recessive hypotrichosis in 13 Pakistani families.
PMID 19292720·Br J Dermatol·2009
8-other
Psychiatric morbidity and domestic violence: a survey of married women in Lahore.
PMID 19277437·Soc Psychiatry Psychiatr Epidemiol·2009
4-observational
INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouse.
PMID 19668215·Nat Genet·2009
7-preclinical
Proteomic analysis of the Trypanosoma cruzi ribosomal proteins.
PMID 19245787·Biochem Biophys Res Commun·2009
7-preclinical
Environmental effects on transglutaminase production and cell sporulation in submerged cultivation of Bacillus circulans.
PMID 18716920·Appl Biochem Biotechnol·2009
8-other
Identifying putative promoter regions of Hermansky-Pudlak syndrome genes by means of phylogenetic footprinting.
PMID 19523149·Ann Hum Genet·2009
8-other
The C-terminal end of P proteins mediates ribosome inactivation by trichosanthin but does not affect the pokeweed antiviral protein activity.
PMID 18282466·Biochem Biophys Res Commun·2008
8-other
A note on plane wave diffraction by a perfectly conducting strip in a homogeneous bi-isotropic medium.
PMID 18711558·Opt Express·2008
8-other
Solid state bioreactor production of transglutaminase by Amazonian Bacillus circulans BL32 strain.
PMID 18696133·J Ind Microbiol Biotechnol·2008
8-other
Production of ethanol from soybean hull hydrolysate by osmotolerant Candida guilliermondii NRRL Y-2075.
PMID 17706417·Bioresour Technol·2008
8-other
Linkage analysis in a large family from Pakistan with depression and a high incidence of consanguineous marriages.
PMID 18506107·Hum Hered·2008
8-other
Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3).
PMID 18461368·Hum Genet·2008
8-other
CC2D2A, encoding a coiled-coil and C2 domain protein, causes autosomal-recessive mental retardation with retinitis pigmentosa.
PMID 18387594·Am J Hum Genet·2008
7-preclinical
Homozygosity mapping in a family presenting with schizophrenia, epilepsy and hearing impairment.
PMID 18322454·Eur J Hum Genet·2008
8-other
Addendum. CC2D2A, encoding a coiled-coil and C2 domain protein, causes autosomal-recessive mental retardation with retinitis pigmentosa.
PMID 19068953·Am J Hum Genet·2008
8-other
Anti-hepatits B core antigen testing, viral markers, and occult hepatitis B virus infection in Pakistani blood donors: implications for transfusion practice.
PMID 17207233·Transfusion·2007
8-other
Biodegradation of the herbicide glyphosate by filamentous fungi in platform shaker and batch bioreactor.
PMID 17978956·J Environ Sci Health B·2007
8-other
Susceptibility of Anthonomus grandis (cotton boll weevil) and Spodoptera frugiperda (fall armyworm) to a cry1ia-type toxin from a Brazilian Bacillus thuringiensis strain.
PMID 17927912·J Biochem Mol Biol·2007
7-preclinical
Localization of a novel autosomal recessive hypotrichosis locus (LAH3) to chromosome 13q14.11-q21.32.
PMID 17594396·Clin Genet·2007
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
- 400 OSBORNE TER, L-4
NEWARK, NJ 07112 - Phone
- (973) 926-7472
Quick Facts
- NPI
- 1710941836
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 37
- Publications
- 20
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