Back to Search
ZAHRAA AHMED, PHARMD, RPH
PHARMD, RPH
Pharmacist
NPI: 1275145872Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
PH237958(MA)
Research & Publications (20)
Cisplatin sensitivity of oral squamous carcinoma cells is regulated by Na+,K+-ATPase activity rather than copper-transporting P-type ATPases, ATP7A and ATP7B.
PMID 18545997·Cancer Chemother Pharmacol·2009
8-other
USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23.
PMID 18505454·Clin Genet·2009
8-other
Clinical and neuropathologic features of progressive supranuclear palsy with severe pallido-nigro-luysial degeneration and axonal dystrophy.
PMID 18158316·Brain·2008
8-other
Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome.
PMID 18719945·Hum Genet·2008
8-other
Combined effects of acrobatic exercise and magnetic stimulation on the functional recovery after spinal cord lesions.
PMID 18986227·J Neurotrauma·2008
7-preclinical
Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.
PMID 18953341·Nat Genet·2008
7-preclinical
Actin-binding proteins coronin-1a and IBA-1 are effective microglial markers for immunohistochemistry.
PMID 17341475·J Histochem Cytochem·2007
4-observational
Progranulin in frontotemporal lobar degeneration and neuroinflammation.
PMID 17291356·J Neuroinflammation·2007
6-review
Detection and seroprevalence of infectious bronchitis virus strains in commercial poultry in Pakistan.
PMID 17575179·Poult Sci·2007
7-preclinical
The tip-link antigen, a protein associated with the transduction complex of sensory hair cells, is protocadherin-15.
PMID 16807332·J Neurosci·2006
7-preclinical
Structure determination of ursene-type triterpenes by NMR techniques.
PMID 16607673·Magn Reson Chem·2006
8-other
Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan.
PMID 15447792·BMC Med Genet·2004
8-other
Suzuki cross-coupling reactions of gamma-alkylidenebutenolides: application to the synthesis of vulpinic acid.
PMID 15153005·J Org Chem·2004
8-other
PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23.
PMID 14570705·Hum Mol Genet·2003
7-preclinical
Interleukin-12 induces mild experimental allergic encephalomyelitis following local central nervous system injury in the Lewis rat.
PMID 12864978·J Neuroimmunol·2003
7-preclinical
Mutations of MYO6 are associated with recessive deafness, DFNB37.
PMID 12687499·Am J Hum Genet·2003
8-other
A role for caspase-1 and -3 in the pathology of experimental allergic encephalomyelitis : inflammation versus degeneration.
PMID 12414506·Am J Pathol·2002
7-preclinical
Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC.
PMID 12107438·Hum Genet·2002
4-observational
Myelin/axonal pathology in interleukin-12 induced serial relapses of experimental allergic encephalomyelitis in the Lewis rat.
PMID 11395390·Am J Pathol·2001
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
- 301 BROADWAY STE P
CHELSEA, MA 02150 - Phone
- (253) 218-0830
Quick Facts
- NPI
- 1275145872
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile