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SALWAT MALIK, M.D.
M.D.
Family Medicine Physician
NPI: 1548421399IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
252850-1(NY)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
OTHER
Class of 1982
Research & Publications (20)
Congenital, low penetrance lymphedema of lower limbs maps to chromosome 6q16.2-q22.1 in an inbred Pakistani family.
PMID 18193458·Hum Genet·2008
8-other
Fifth finger camptodactyly maps to chromosome 3q11.2-q13.12 in a large German kindred.
PMID 18000522·Eur J Hum Genet·2008
8-other
Identification of a regulator of transcription elongation as an accessory factor for the human Mediator coactivator.
PMID 17404243·Proc Natl Acad Sci U S A·2007
4-observational
Synpolydactyly and HOXD13 polyalanine repeat: addition of 2 alanine residues is without clinical consequences.
PMID 18072967·BMC Med Genet·2007
8-other
Genetic heterogeneity of synpolydactyly: a novel locus SPD3 maps to chromosome 14q11.2-q12.
PMID 16712704·Clin Genet·2006
8-other
Lamotrigine and its applications in the treatment of epilepsy and other neurological and psychiatric disorders.
PMID 17144777·Expert Rev Neurother·2006
6-review
Dynamic regulation of pol II transcription by the mammalian Mediator complex.
PMID 15896744·Trends Biochem Sci·2005
6-review
A simple method for characterising syndactyly in clinical practice.
PMID 16261692·Genet Couns·2005
8-other
Evidence for clinical and genetic heterogeneity of syndactyly type I: the phenotype of second and third toe syndactyly maps to chromosome 3p21.31.
PMID 16189548·Eur J Hum Genet·2005
8-other
Ric-8 enhances G protein betagamma-dependent signaling in response to betagamma-binding peptides in intact cells.
PMID 15802611·Mol Pharmacol·2005
7-preclinical
Autosomal recessive mesoaxial synostotic syndactyly with phalangeal reduction maps to chromosome 17p13.3.
PMID 15779011·Am J Med Genet A·2005
8-other
Structural and functional characterization of PC2 and RNA polymerase II-associated subpopulations of metazoan Mediator.
PMID 15743810·Mol Cell Biol·2005
8-other
Structural and functional organization of TRAP220, the TRAP/mediator subunit that is targeted by nuclear receptors.
PMID 15340084·Mol Cell Biol·2004
7-preclinical
A novel type of autosomal recessive syndactyly: clinical and molecular studies in a family of Pakistani origin.
PMID 15039974·Am J Med Genet A·2004
5-case
TRAP/SMCC/mediator-dependent transcriptional activation from DNA and chromatin templates by orphan nuclear receptor hepatocyte nuclear factor 4.
PMID 12101254·Mol Cell Biol·2002
8-other
First direct discrimination of chiral phosphine selenide (P=Se) derivatives by multinuclear magnetic resonance spectroscopy in the presence of a chiral dirhodium complex.
PMID 11984756·Chirality·2002
8-other
Transcriptional regulation through Mediator-like coactivators in yeast and metazoan cells.
PMID 10838567·Trends Biochem Sci·2000
6-review
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 535 MAIN ST STE 1
OLEAN, NY 14760 - Phone
- (716) 372-0141
Quick Facts
- NPI
- 1548421399
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 44
- Publications
- 20
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