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L N Clark

Showing results (21-30 of 28) with videos related to

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Genomics|May 23, 1998
A novel long and unstable CAG/CTG trinucleotide repeat on chromosome 17qT Ikeuchi, K Sanpei, H Takano, et al.
ESMO Open|April 19, 2024
A phase I study to evaluate the safety, pharmacokinetics, and pharmacodynamics of PF-06939999 (PRMT5 inhibitor) in patients with selected advanced or metastatic tumors with high incidence of splicing factor gene mutationsJ Rodon, E Rodriguez, M L Maitland, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 28, 1998
Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17L N Clark, P Poorkaj, Z Wszolek, et al.
Neurology|January 6, 2011
Olfaction in Parkin heterozygotes and compound heterozygotes: the CORE-PD studyR N Alcalay, A Siderowf, R Ottman, et al.
Parkinsonism & Related Disorders|August 23, 2011
The relation between depression and parkin genotype: the CORE-PD studyA Srivastava, M-X Tang, H Mejia-Santana, et al.
Neurology|March 24, 2012
Cognitive performance of GBA mutation carriers with early-onset PD: the CORE-PD studyR N Alcalay, E Caccappolo, H Mejia-Santana, et al.
The New England Journal of Medicine|October 23, 2009
Multicenter analysis of glucocerebrosidase mutations in Parkinson's diseaseE Sidransky, M A Nalls, J O Aasly, et al.
Nature|January 10, 2002
The DNA sequence and comparative analysis of human chromosome 20P Deloukas, L H Matthews, J Ashurst, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Genomics|May 23, 1998
A novel long and unstable CAG/CTG trinucleotide repeat on chromosome 17qT Ikeuchi, K Sanpei, H Takano, et al.
ESMO Open|April 19, 2024
A phase I study to evaluate the safety, pharmacokinetics, and pharmacodynamics of PF-06939999 (PRMT5 inhibitor) in patients with selected advanced or metastatic tumors with high incidence of splicing factor gene mutationsJ Rodon, E Rodriguez, M L Maitland, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 28, 1998
Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17L N Clark, P Poorkaj, Z Wszolek, et al.
Neurology|January 6, 2011
Olfaction in Parkin heterozygotes and compound heterozygotes: the CORE-PD studyR N Alcalay, A Siderowf, R Ottman, et al.
Parkinsonism & Related Disorders|August 23, 2011
The relation between depression and parkin genotype: the CORE-PD studyA Srivastava, M-X Tang, H Mejia-Santana, et al.
Neurology|March 24, 2012
Cognitive performance of GBA mutation carriers with early-onset PD: the CORE-PD studyR N Alcalay, E Caccappolo, H Mejia-Santana, et al.
The New England Journal of Medicine|October 23, 2009
Multicenter analysis of glucocerebrosidase mutations in Parkinson's diseaseE Sidransky, M A Nalls, J O Aasly, et al.
Nature|January 10, 2002
The DNA sequence and comparative analysis of human chromosome 20P Deloukas, L H Matthews, J Ashurst, et al.
Pageof 3