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DAYA KUMARI, M.D.
M.D.
Student in an Organized Health Care Education/Training Program
NPI: 1376438556Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (16)
Chromatin remodeling in the noncoding repeat expansion diseases.
PMID 18957431·J Biol Chem·2009
6-review
The role of DNA damage response pathways in chromosome fragility in Fragile X syndrome.
PMID 19465392·Nucleic Acids Res·2009
8-other
SIRT1 inhibition alleviates gene silencing in Fragile X mental retardation syndrome.
PMID 18369442·PLoS Genet·2008
8-other
Effect on histological and sperm kinetics in DBP exposed Wistar rats.
PMID 19295080·J Environ Biol·2008
7-preclinical
Repeat-induced epigenetic changes in intron 1 of the frataxin gene and its consequences in Friedreich ataxia.
PMID 17478498·Nucleic Acids Res·2007
8-other
Rice (Oryza sativa) allergy in rhinitis and asthma patients: a clinico-immunological study.
PMID 17336834·Immunobiology·2007
8-other
Sensitization to blackgram in patients with bronchial asthma and rhinitis: clinical evaluation and characterization of allergens.
PMID 16364164·Allergy·2006
4-observational
Ancient repeated DNA elements and the regulation of the human frataxin promoter.
PMID 15676280·Genomics·2005
7-preclinical
Long CGG-repeat tracts are toxic to human cells: implications for carriers of Fragile X premutation alleles.
PMID 15862312·FEBS Lett·2005
4-observational
The roles of Sp1, Sp3, USF1/USF2 and NRF-1 in the regulation and three-dimensional structure of the Fragile X mental retardation gene promoter.
PMID 15479157·Biochem J·2005
7-preclinical
Deletion analysis of the dystrophin gene in Duchenne and Becker muscular dystrophy patients: use in carrier diagnosis.
PMID 14571009·Neurol India·2003
8-other
Instability of the fragile X syndrome repeat in mice: the effect of age, diet and mutations in genes that affect DNA replication, recombination and repair proficiency.
PMID 14526174·Cytogenet Genome Res·2003
7-preclinical
Transcription defects induced by repeat expansion: fragile X syndrome, FRAXE mental retardation, progressive myoclonus epilepsy type 1, and Friedreich ataxia.
PMID 14526165·Cytogenet Genome Res·2003
6-review
Interaction of the transcription factors USF1, USF2, and alpha -Pal/Nrf-1 with the FMR1 promoter. Implications for Fragile X mental retardation syndrome.
PMID 11058604·J Biol Chem·2001
7-preclinical
Detection of deletion in the dystrophin gene of a patient with quadriceps myopathy.
PMID 10751817·Neurol India·2000
5-case
A variation in the HINDIII restriction pattern of the dystrophin gene DMD with cDMD probe 11-14.
PMID 10649500·Hum Mutat·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
- 2500 N STATE STREET
JACKSON, MS 39216 - Phone
- (601) 984-5426
Quick Facts
- NPI
- 1376438556
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 16
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