Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Novel P-TEN-induced putative kinase 1 (PINK1) variant in Indian Parkinson's disease patient.

Neuroscience letters - 25 Sept 2015

Halder Tamali, Raj Janak, Sharma Vivek, Das Parimal

Abstract excerpt

Loss-of-function mutation in PINK1 is known for causing autosomal recessive early onset Parkinsonism accounting approximately 6.5% of PD cases. Recently, PINK1 has also been shown to cause Parkinson's disease (PD) in eastern India. Present study is aimed to see its contribution in north-Indian PD patients. A total of 106 PD patients and 60 ethnically matched healthy controls were included in the study. All the...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Amino Acid Sequence
Share to Case-Control Studies
Share to Chlorocebus aethiops

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to COS Cells

Share to Molecular Sequence Data

Share to Parkinson Disease

Share to Protein Kinases

Source

Identifiers

PMID: 26282903
DOI: 10.1016/j.neulet.2015.08.021

Genes

PINK1

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Novel P-TEN-induced putative kinase 1 (PINK1) variant in Indian Parkinson's disease patient.PMID 26282903Read ↗

Mutations in PTEN-induced putative kinase 1 associated with recessive parkinsonism have differential effects on protein stabilitySemantic proximity Read ↗

A Novel PINK1 p.F385S Loss-of-Function Mutation in an Indian Family with Parkinson's Disease.Semantic proximity Read ↗

The emerging multifaceted role of PINK1 in cancer biologySemantic proximity Read ↗

Mutation analysis of PINK1 gene in patients with early-onset Parkinsonism.Semantic proximity Read ↗

Biochemical aspects of the neuroprotective mechanism of PTEN-induced kinase-1 (PINK1).Semantic proximity Read ↗

Rethinking 'rare' PINK1 Parkinson's disease: A meta-analysis of geographical prevalence, phenotypic diversity, and α-synuclein pathology.Semantic proximity Read ↗

Identification of Kinase inhibitors as PINK1 activators for the treatment of Parkinson’s DiseaseSemantic proximity Read ↗

Molecular pathogenesis of Parkinson's disease: identification of mutations in the Parkin gene in Indian patients.Semantic proximity Read ↗

Systematic Functional Analysis of PINK1 and PRKN Coding VariantsSemantic proximity Read ↗

Discovery of catalytically active orthologues of the Parkinson's disease kinase PINK1: analysis of substrate specificity and impact of mutationsSemantic proximity Read ↗

Analysis of the PINK1 Gene in a Large Cohort of Cases With Parkinson DiseaseSemantic proximity Read ↗

Rare and novel variants of PRKN and PINK1 genes in Vietnamese patients with early-onset Parkinson's disease.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.