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M Prakash

Showing results (301-310 of 319) with videos related to

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Molecular Cancer Therapeutics|November 9, 2007
Progressive loss of epidermal growth factor receptor in a subpopulation of breast cancers: implications in target-directed therapeuticsLee-Yee Choong, Simin Lim, Marie Chiew-Shia Loh, et al.
Clinical Genetics|October 23, 2012
Association of HLA locus variant in Parkinson's diseaseY Zhao, A A Gopalai, A Ahmad-Annuar, et al.
Frontiers in Aging Neuroscience|December 13, 2023
Quantitative iron-neuromelanin MRI associates with motor severity in Parkinson's disease and matches radiological disease classificationSeptian Hartono, Robert Chun Chen, Thomas Welton, et al.
Neurobiology of Aging|May 9, 2013
Absence of A673T amyloid-β precursor protein variant in Alzheimer's disease and other neurological diseasesSimon Kang Seng Ting, Mei-Sian Chong, Nagaendran Kandiah, et al.
Human Mutation|February 27, 2010
Multiple LRRK2 variants modulate risk of Parkinson disease: a Chinese multicenter studyEng-King Tan, Rong Peng, Yik-Ying Teo, et al.
Journal of Parkinson'S Disease|February 20, 2025
Rare <i>SV2C</i> coding variants in Parkinson's disease riskChu Hua Chang, Elaine Guo Yan Chew, Michelle Mulan Lian, et al.
Neurology|July 15, 2011
Phenotype in parkinsonian and nonparkinsonian LRRK2 G2019S mutation carriersC Marras, B Schüle, B Schuele, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 22, 2015
Linking a genome-wide association study signal to a LRRK2 coding variant in Parkinson's diseaseJia Nee Foo, Sun Ju Chung, Louis C Tan, et al.
Annals of Neurology|June 5, 2020
NOTCH2NLC GGC Repeat Expansions Are Associated with Sporadic Essential Tremor: Variable Disease Expressivity on Long-Term Follow-upAdeline S L Ng, Weng Khong Lim, Zheyu Xu, et al.
Human Molecular Genetics|February 26, 2014
Analysis of non-synonymous-coding variants of Parkinson's disease-related pathogenic and susceptibility genes in East Asian populationsJia Nee Foo, Louis C Tan, Herty Liany, et al.
Pageof 32

Showing results (301-310 of 319) with videos related to

Sort By:
Pageof 32
Molecular Cancer Therapeutics|November 9, 2007
Progressive loss of epidermal growth factor receptor in a subpopulation of breast cancers: implications in target-directed therapeuticsLee-Yee Choong, Simin Lim, Marie Chiew-Shia Loh, et al.
Clinical Genetics|October 23, 2012
Association of HLA locus variant in Parkinson's diseaseY Zhao, A A Gopalai, A Ahmad-Annuar, et al.
Frontiers in Aging Neuroscience|December 13, 2023
Quantitative iron-neuromelanin MRI associates with motor severity in Parkinson's disease and matches radiological disease classificationSeptian Hartono, Robert Chun Chen, Thomas Welton, et al.
Neurobiology of Aging|May 9, 2013
Absence of A673T amyloid-β precursor protein variant in Alzheimer's disease and other neurological diseasesSimon Kang Seng Ting, Mei-Sian Chong, Nagaendran Kandiah, et al.
Human Mutation|February 27, 2010
Multiple LRRK2 variants modulate risk of Parkinson disease: a Chinese multicenter studyEng-King Tan, Rong Peng, Yik-Ying Teo, et al.
Journal of Parkinson'S Disease|February 20, 2025
Rare <i>SV2C</i> coding variants in Parkinson's disease riskChu Hua Chang, Elaine Guo Yan Chew, Michelle Mulan Lian, et al.
Neurology|July 15, 2011
Phenotype in parkinsonian and nonparkinsonian LRRK2 G2019S mutation carriersC Marras, B Schüle, B Schuele, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 22, 2015
Linking a genome-wide association study signal to a LRRK2 coding variant in Parkinson's diseaseJia Nee Foo, Sun Ju Chung, Louis C Tan, et al.
Annals of Neurology|June 5, 2020
NOTCH2NLC GGC Repeat Expansions Are Associated with Sporadic Essential Tremor: Variable Disease Expressivity on Long-Term Follow-upAdeline S L Ng, Weng Khong Lim, Zheyu Xu, et al.
Human Molecular Genetics|February 26, 2014
Analysis of non-synonymous-coding variants of Parkinson's disease-related pathogenic and susceptibility genes in East Asian populationsJia Nee Foo, Louis C Tan, Herty Liany, et al.
Pageof 32