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JENICA CHANDRAN, DO
DO
Internal Medicine Physician
NPI: 1841878915IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
330115(NY)
CMS Specialties
PrimaryINTERNAL MEDICINE
Education
OTHER
Class of 2021
Research & Publications (16)
Regulation of endosomal motility and degradation by amyotrophic lateral sclerosis 2/alsin.
PMID 19630956·Mol Brain·2009
7-preclinical
Novel foldamer structural architecture from cofacial aromatic building blocks.
PMID 19503899·Chem Commun (Camb)·2009
8-other
Sterically controlled naphthalene homo-oligoamides with novel structural architectures.
PMID 19462058·Org Biomol Chem·2009
8-other
Comparison of receptor binding characteristics of commonly used muscarinic antagonists in human bladder detrusor and mucosa.
PMID 19029429·J Pharmacol Exp Ther·2009
8-other
RNA binding activity of the recessive parkinsonism protein DJ-1 supports involvement in multiple cellular pathways.
PMID 18626009·Proc Natl Acad Sci U S A·2008
7-preclinical
The chaperone activity of heat shock protein 90 is critical for maintaining the stability of leucine-rich repeat kinase 2.
PMID 18367605·J Neurosci·2008
7-preclinical
DJ-1 is essential for long-term depression at hippocampal CA1 synapses.
PMID 18246449·Neuromolecular Med·2008
7-preclinical
Progressive behavioral deficits in DJ-1-deficient mice are associated with normal nigrostriatal function.
PMID 18187333·Neurobiol Dis·2008
4-observational
The G59S mutation in p150(glued) causes dysfunction of dynactin in mice.
PMID 18094236·J Neurosci·2007
4-observational
Alsin and the molecular pathways of amyotrophic lateral sclerosis.
PMID 17955197·Mol Neurobiol·2007
6-review
Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans.
PMID 17590087·PLoS Genet·2007
7-preclinical
Amyotrophic lateral sclerosis 2-deficiency leads to neuronal degeneration in amyotrophic lateral sclerosis through altered AMPA receptor trafficking.
PMID 17093100·J Neurosci·2006
4-observational
L166P mutant DJ-1, causative for recessive Parkinson's disease, is degraded through the ubiquitin-proteasome system.
PMID 12851414·J Biol Chem·2003
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
- 110 E. 58TH STREET, SUITE 400
NEW YORK, NY 10022 - Phone
- (646) 785-8150
Quick Facts
- NPI
- 1841878915
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 5
- Publications
- 16
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