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ISLAM GHAZI, PHARMD
PHARMD
Pharmacist Clinician (PhC)/ Clinical Pharmacy Specialist
NPI: 1245836295Individual
Specialties, Licenses & Credentials
Pharmacist Clinician (PhC)/ Clinical Pharmacy SpecialistPrimary
Pharmacist — Pharmacist Clinician (PhC)/ Clinical Pharmacy Specialist
Code: 1835P0018X
RP451359(PA)
Research & Publications (12)
Physical mapping, expression analysis and polymorphism survey of resistance gene analogues on chromosome 11 of rice.
PMID 19550041·J Biosci·2009
8-other
Catalytic role of conserved HQGE motif in the CE6 carbohydrate esterase family.
PMID 17826771·FEBS Lett·2007
7-preclinical
Biochemical and structural features of a novel cyclodextrinase from cow rumen metagenome.
PMID 17238236·Biotechnol J·2007
7-preclinical
Purification and kinetic characterization of a fructosyltransferase from Aspergillus aculeatus.
PMID 17056145·J Biotechnol·2007
8-other
Single-copy genes define a conserved order between rice and wheat for understanding differences caused by duplication, deletion, and transposition of genes.
PMID 16865332·Funct Integr Genomics·2007
4-observational
Beet sugar syrup and molasses as low-cost feedstock for the enzymatic production of fructo-oligosaccharides.
PMID 16608216·J Agric Food Chem·2006
8-other
Purification and properties of a novel extra-cellular thermotolerant metallolipase of Bacillus coagulans MTCC-6375 isolate.
PMID 16290008·Protein Expr Purif·2006
8-other
Properties of an immobilized lipase of Bacillus coagulans BTS-1.
PMID 15362288·Acta Microbiol Immunol Hung·2004
8-other
Sequence analysis of the long arm of rice chromosome 11 for rice-wheat synteny.
PMID 15085449·Funct Integr Genomics·2004
8-other
Dominant X linked retinitis pigmentosa is frequently accounted for by truncating mutations in exon ORF15 of the RPGR gene.
PMID 11950860·J Med Genet·2002
8-other
Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosis.
PMID 11528500·Eur J Hum Genet·2001
7-preclinical
Spectrum of retGC1 mutations in Leber's congenital amaurosis.
PMID 10951519·Eur J Hum Genet·2000
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
- 3 COOPER PLZ
CAMDEN, NJ 08103 - Phone
- (800) 826-6737
Quick Facts
- NPI
- 1245836295
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 12
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