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F Mata

Showing results (231-240 of 293) with videos related to

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Arquivos De Neuro-Psiquiatria|September 1, 2021
Genetics of Parkinson's disease in Brazil: a systematic review of monogenic formsBruno L Santos-Lobato, Artur Schumacher-Schuh, Ignacio F Mata, et al.
Pediatric Blood & Cancer|March 17, 2010
Low mRNA expression of the apoptosis-related genes CASP3, CASP8, and FAS is associated with low induction treatment response in childhood acute lymphoblastic leukemia (ALL)Juliana F Mata, Vanessa S Silveira, Elvis C Mateo, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 12, 2007
Pathogenicity of the Lrrk2 R1514Q substitution in Parkinson's diseaseMathias Toft, Ignacio F Mata, Owen A Ross, et al.
Biorxiv : the Preprint Server for Biology|January 20, 2025
Subcontinental Genetic Diversity in the <i>All of Us</i> Research Program: Implications for Biomedical ResearchMateus H Gouveia, Karlijn A C Meeks, Victor Borda, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 23, 2011
Replication of MAPT and SNCA, but not PARK16-18, as susceptibility genes for Parkinson's diseaseIgnacio F Mata, Dora Yearout, Victoria Alvarez, et al.
American Journal of Human Genetics|June 6, 2025
Subcontinental genetic variation in the All of Us Research Program: Implications for biomedical researchMateus H Gouveia, Karlijn A C Meeks, Victor Borda, et al.
Parkinsonism & Related Disorders|June 2, 2007
Lrrk2-associated parkinsonism is a major cause of disease in Northern SpainMaría C González-Fernández, Elena Lezcano, Owen A Ross, et al.
American Journal of Human Genetics|February 24, 2005
Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populationsJennifer Kachergus, Ignacio F Mata, Mary Hulihan, et al.
Frontiers in Neurology|October 5, 2020
Sensorimotor Inhibition and Mobility in Genetic Subgroups of Parkinson's DiseaseDouglas N Martini, Rosie Morris, Valerie E Kelly, et al.
Annals of Neurology|April 17, 2008
Analysis of Lrrk2 R1628P as a risk factor for Parkinson's diseaseOwen A Ross, Yih-Ru Wu, Mei-Ching Lee, et al.
Pageof 30

Showing results (231-240 of 293) with videos related to

Sort By:
Pageof 30
Arquivos De Neuro-Psiquiatria|September 1, 2021
Genetics of Parkinson's disease in Brazil: a systematic review of monogenic formsBruno L Santos-Lobato, Artur Schumacher-Schuh, Ignacio F Mata, et al.
Pediatric Blood & Cancer|March 17, 2010
Low mRNA expression of the apoptosis-related genes CASP3, CASP8, and FAS is associated with low induction treatment response in childhood acute lymphoblastic leukemia (ALL)Juliana F Mata, Vanessa S Silveira, Elvis C Mateo, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 12, 2007
Pathogenicity of the Lrrk2 R1514Q substitution in Parkinson's diseaseMathias Toft, Ignacio F Mata, Owen A Ross, et al.
Biorxiv : the Preprint Server for Biology|January 20, 2025
Subcontinental Genetic Diversity in the <i>All of Us</i> Research Program: Implications for Biomedical ResearchMateus H Gouveia, Karlijn A C Meeks, Victor Borda, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 23, 2011
Replication of MAPT and SNCA, but not PARK16-18, as susceptibility genes for Parkinson's diseaseIgnacio F Mata, Dora Yearout, Victoria Alvarez, et al.
American Journal of Human Genetics|June 6, 2025
Subcontinental genetic variation in the All of Us Research Program: Implications for biomedical researchMateus H Gouveia, Karlijn A C Meeks, Victor Borda, et al.
Parkinsonism & Related Disorders|June 2, 2007
Lrrk2-associated parkinsonism is a major cause of disease in Northern SpainMaría C González-Fernández, Elena Lezcano, Owen A Ross, et al.
American Journal of Human Genetics|February 24, 2005
Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populationsJennifer Kachergus, Ignacio F Mata, Mary Hulihan, et al.
Frontiers in Neurology|October 5, 2020
Sensorimotor Inhibition and Mobility in Genetic Subgroups of Parkinson's DiseaseDouglas N Martini, Rosie Morris, Valerie E Kelly, et al.
Annals of Neurology|April 17, 2008
Analysis of Lrrk2 R1628P as a risk factor for Parkinson's diseaseOwen A Ross, Yih-Ru Wu, Mei-Ching Lee, et al.
Pageof 30