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MUHAMMAD DANYAL TARIQ, M.D
M.D
Student in an Organized Health Care Education/Training Program
NPI: 1104674902Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Clinical Trials (1)
1
Linked Trials
0
Recruiting
1
With Results
Research & Publications (20)
WNT10A missense mutation associated with a complete odonto-onycho-dermal dysplasia syndrome.
PMID 19471313·Eur J Hum Genet·2009
8-other
Pentoxifylline attenuates iminodipropionitrile-induced behavioral abnormalities in rats.
PMID 19584713·Behav Pharmacol·2009
7-preclinical
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
Chromium chloride administration causes a substantial reduction of coronary lipid deposits, aortic lipid deposits, and serum cholesterol concentration in rabbits.
PMID 19225722·Biol Trace Elem Res·2009
7-preclinical
Haplotype analysis of two X-chromosome STR clusters in the Pakistani population.
PMID 19011887·Int J Legal Med·2009
8-other
Relationship between anti-acetylcholine receptor antibody titres and severity of myasthenia gravis.
PMID 19438131·J Pak Med Assoc·2009
4-observational
Outbreak of dengue fever in Karachi 2006: a clinical perspective.
PMID 19534364·J Pak Med Assoc·2009
8-other
Recurrent mutations in functionally-related EDA and EDAR genes underlie X-linked isolated hypodontia and autosomal recessive hypohidrotic ectodermal dysplasia.
PMID 19551394·Arch Dermatol Res·2009
8-other
Mutations in the P2RY5 gene underlie autosomal recessive hypotrichosis in 13 Pakistani families.
PMID 19292720·Br J Dermatol·2009
8-other
Trithorax requires Hsp90 for maintenance of active chromatin at sites of gene expression.
PMID 19144915·Proc Natl Acad Sci U S A·2009
7-preclinical
Impact of prior antibiotic use in culture-negative endocarditis: review of 86 cases from southern Pakistan.
PMID 19131263·Int J Infect Dis·2009
8-other
Ectodermal dysplasia-cutaneous syndactyly syndrome maps to chromosome 7p21.1-p14.3.
PMID 19221800·Hum Genet·2009
5-case
Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3).
PMID 18461368·Hum Genet·2008
8-other
Association of Interleukin-10 gene promoter polymorphisms in Saudi patients with vitiligo.
PMID 18057536·Dis Markers·2008
8-other
A syndromic form of autosomal recessive congenital microcephaly (Jawad syndrome) maps to chromosome 18p11.22-q11.2.
PMID 18071751·Hum Genet·2008
8-other
Career goals of trainee physicians in internal medicine.
PMID 18760046·J Coll Physicians Surg Pak·2008
8-other
Effects of subchronic versus acute in utero exposure to dexmedetomidine on foetal developments in rats.
PMID 18816303·Basic Clin Pharmacol Toxicol·2008
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
- 12101 CAROL LANE, SUITE 101 MWHC FAMILY MEDICINE RESIDE
FREDERICKSBURG, VA 22407 - Phone
- (540) 418-6681
Quick Facts
- NPI
- 1104674902
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Clinical Trials
- 1
- Publications
- 20
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