Back to Search
GHOLAM ALI, MD
MD
Cardiovascular Disease Physician
NPI: 1851493803Individual
Specialties, Licenses & Credentials
Cardiovascular Disease PhysicianPrimary
Internal Medicine — Cardiovascular Disease
Code: 207RC0000X
14879R(LA)
Research & Publications (20)
Analyses of in vivo interaction and mobility of two spliceosomal proteins using FRAP and BiFC.
PMID 18414657·PLoS One·2008
8-other
Regulation of plant developmental processes by a novel splicing factor.
PMID 17534421·PLoS One·2007
8-other
A mutation in the lipase H (LIPH) gene underlie autosomal recessive hypotrichosis.
PMID 17333281·Hum Genet·2007
8-other
Ligand-dependent reduction in the membrane mobility of FLAGELLIN SENSITIVE2, an arabidopsis receptor-like kinase.
PMID 17925310·Plant Cell Physiol·2007
8-other
ATP, phosphorylation and transcription regulate the mobility of plant splicing factors.
PMID 16895966·J Cell Sci·2006
8-other
The mapping of DFNB62, a new locus for autosomal recessive non-syndromic hearing impairment, to chromosome 12p13.2-p11.23.
PMID 16650082·Clin Genet·2006
8-other
Nuclear localization and in vivo dynamics of a plant-specific serine/arginine-rich protein.
PMID 14675452·Plant J·2003
8-other
Differential expression of genes encoding calmodulin-binding proteins in response to bacterial pathogens and inducers of defense responses.
PMID 12777041·Plant Mol Biol·2003
8-other
Inhibition of fungal and bacterial plant pathogens by synthetic peptides: in vitro growth inhibition, interaction between peptides and inhibition of disease progression.
PMID 10939256·Mol Plant Microbe Interact·2000
8-other
How to establish a successful revolving drug fund: the experience of Khartoum state in the Sudan.
PMID 19274366·Bull World Health Organ·2009
8-other
Mutations in the P2RY5 gene underlie autosomal recessive hypotrichosis in 13 Pakistani families.
PMID 19292720·Br J Dermatol·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
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 missense mutations in lipase H (LIPH) gene causing autosomal recessive hypotrichosis (LAH2).
PMID 19167195·J Dermatol Sci·2009
8-other
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
PMID 19576567·Am J Hum Genet·2009
7-preclinical
First report of chikungunya from the Maldives.
PMID 18930301·Trans R Soc Trop Med Hyg·2009
7-preclinical
Callus induction and in vitro plant regeneration of rice (Oryza sativa L.) under various conditions.
PMID 18817199·Pak J Biol Sci·2008
8-other
A novel insertion mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene underlies Grebe-type chondrodysplasia in a consanguineous Pakistani family.
PMID 19038017·BMC Med Genet·2008
8-other
Serum retinol binding protein as an indicator of vitamin A status in cirrhotic patients with night blindness.
PMID 19568486·Saudi J Gastroenterol·2008
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
- 1415 TULANE AVE
NEW ORLEANS, LA 70112 - Phone
- (504) 988-5152
Quick Facts
- NPI
- 1851493803
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile