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MOHAMMED CHISHTI, M.D
M.D
Student in an Organized Health Care Education/Training Program
NPI: 1982341541Individual
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)
Gastro-intestinal nematode infections in goats relative to season, host sex and age from the Kashmir valley, India.
PMID 19627625·J Helminthol·2010
7-preclinical
Anthelmintic activity of extracts of Artemisia absinthium against ovine nematodes.
PMID 19070963·Vet Parasitol·2009
7-preclinical
Mutations in the P2RY5 gene underlie autosomal recessive hypotrichosis in 13 Pakistani families.
PMID 19292720·Br J Dermatol·2009
8-other
Mutation in the HPGD gene encoding NAD+ dependent 15-hydroxyprostaglandin dehydrogenase underlies isolated congenital nail clubbing (ICNC).
PMID 18805827·J Med Genet·2009
8-other
Novel autosomal recessive non-syndromic hearing impairment locus (DFNB71) maps to chromosome 8p22-21.3.
PMID 19229252·J Hum Genet·2009
8-other
Splice-site mutations in the TRIC gene underlie autosomal recessive nonsyndromic hearing impairment in Pakistani families.
PMID 18084694·J Hum Genet·2008
4-observational
Evaluation of anthelmintic activity of Iris hookeriana against gastrointestinal nematodes of sheep.
PMID 18252019·J Helminthol·2008
7-preclinical
Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3).
PMID 18461368·Hum Genet·2008
8-other
The epidemiology of paramphistomosis of sheep (Ovis aries L.) in the north west temperate Himalayan region of India.
PMID 18357509·Vet Res Commun·2008
7-preclinical
Microvascular injury, thrombosis, inflammation, and apoptosis in the pathogenesis of heatstroke: a study in baboon model.
PMID 18388331·Arterioscler Thromb Vasc Biol·2008
7-preclinical
A novel deletion mutation in LIPH gene causes autosomal recessive hypotrichosis (LAH2).
PMID 18445047·Clin Genet·2008
8-other
A novel locus for ectodermal dysplasia of hairs, nails and teeth type maps to chromosome 18q22.1-22.3.
PMID 18184143·Ann Hum Genet·2008
8-other
Epidemiology of gastrointestinal nematodes of sheep managed under traditional husbandry system in Kashmir valley.
PMID 18838225·Vet Parasitol·2008
7-preclinical
A syndromic form of autosomal recessive congenital microcephaly (Jawad syndrome) maps to chromosome 18p11.22-q11.2.
PMID 18071751·Hum Genet·2008
8-other
A novel missense mutation in RSPO4 gene underlies autosomal recessive congenital anonychia in a consanguineous Pakistani family.
PMID 18070203·Br J Dermatol·2008
5-case
Anthelmintic efficacy of Achillea millifolium against gastrointestinal nematodes of sheep: in vitro and in vivo studies.
PMID 18419857·J Helminthol·2008
7-preclinical
Mapping of a gene for alopecia with mental retardation syndrome (APMR3) on chromosome 18q11.2-q12.2.
PMID 17451405·Ann Hum Genet·2007
8-other
Localization of a novel autosomal recessive hypotrichosis locus (LAH3) to chromosome 13q14.11-q21.32.
PMID 17594396·Clin Genet·2007
8-other
Crural tunica albuginea autograft for corporoplasty: an experimental animal study of hemodynamic, histopathological, and molecular effects in the long term.
PMID 17655656·J Sex Med·2007
7-preclinical
Previously described sequence variant in CDK5RAP2 gene in a Pakistani family with autosomal recessive primary microcephaly.
PMID 17764569·BMC Med 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
- VILLA 29 24B STREET AL WARQA 2
DUBAI, DUBAI 04545 - Phone
- (971) 569-1491
Quick Facts
- NPI
- 1982341541
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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