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Showing results (351-360 of 363) with videos related to

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American Journal of Physiology. Cell Physiology|June 3, 2024
Mitochondrial sequencing identifies long noncoding RNA features that promote binding to PNPaseAndrew D Taylor, Quincy A Hathaway, Amina Kunovac, et al.
British Journal of Cancer|August 17, 2000
A phase II study of temozolomide vs. procarbazine in patients with glioblastoma multiforme at first relapseW K Yung, R E Albright, J Olson, et al.
JAMA Network Open|January 18, 2022
Racial and Ethnic Disparities in Prostate Cancer Outcomes in the Veterans Affairs Health Care SystemKosj Yamoah, Kyung Min Lee, Shivanshu Awasthi, et al.
Neurology. Genetics|February 25, 2025
The Spastic Paraplegia-Centers of Excellence Research Network (SP-CERN): Clinical Trial Readiness for Hereditary Spastic ParaplegiaLuca Schierbaum, Vicente Quiroz, Kathryn Yang, et al.
Annals of the American Thoracic Society|March 8, 2023
Lung Function Decline in Cystic Fibrosis: Impact of Data Availability and Modeling Strategies on Clinical InterpretationsRhonda Szczesniak, Eleni-Rosalina Andrinopoulou, Weiji Su, et al.
Cytogenetics and Cell Genetics|May 27, 1999
Report of the fourth international workshop on human chromosome 15 mapping 1997C C Morton, S L Christian, T A Donlon, et al.
American Journal of Human Genetics|July 29, 2014
The Alu-rich genomic architecture of SPAST predisposes to diverse and functionally distinct disease-associated CNV allelesPhilip M Boone, Bo Yuan, Ian M Campbell, et al.
Neurogenetics|June 2, 2011
Call for participation in the neurogenetics consortium within the Human Variome ProjectAndrea Haworth, Lars Bertram, Paola Carrera, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 6, 2025
Toward therapeutic trials in primary lateral sclerosisErica Scirocco, Matti D Allen, Elisa Giacomelli, et al.
Human Mutation|July 17, 2013
Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12Guida Landouré, Peng-Peng Zhu, Charles M Lourenço, et al.
Pageof 37

Showing results (351-360 of 363) with videos related to

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Pageof 37
American Journal of Physiology. Cell Physiology|June 3, 2024
Mitochondrial sequencing identifies long noncoding RNA features that promote binding to PNPaseAndrew D Taylor, Quincy A Hathaway, Amina Kunovac, et al.
British Journal of Cancer|August 17, 2000
A phase II study of temozolomide vs. procarbazine in patients with glioblastoma multiforme at first relapseW K Yung, R E Albright, J Olson, et al.
JAMA Network Open|January 18, 2022
Racial and Ethnic Disparities in Prostate Cancer Outcomes in the Veterans Affairs Health Care SystemKosj Yamoah, Kyung Min Lee, Shivanshu Awasthi, et al.
Neurology. Genetics|February 25, 2025
The Spastic Paraplegia-Centers of Excellence Research Network (SP-CERN): Clinical Trial Readiness for Hereditary Spastic ParaplegiaLuca Schierbaum, Vicente Quiroz, Kathryn Yang, et al.
Annals of the American Thoracic Society|March 8, 2023
Lung Function Decline in Cystic Fibrosis: Impact of Data Availability and Modeling Strategies on Clinical InterpretationsRhonda Szczesniak, Eleni-Rosalina Andrinopoulou, Weiji Su, et al.
Cytogenetics and Cell Genetics|May 27, 1999
Report of the fourth international workshop on human chromosome 15 mapping 1997C C Morton, S L Christian, T A Donlon, et al.
American Journal of Human Genetics|July 29, 2014
The Alu-rich genomic architecture of SPAST predisposes to diverse and functionally distinct disease-associated CNV allelesPhilip M Boone, Bo Yuan, Ian M Campbell, et al.
Neurogenetics|June 2, 2011
Call for participation in the neurogenetics consortium within the Human Variome ProjectAndrea Haworth, Lars Bertram, Paola Carrera, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 6, 2025
Toward therapeutic trials in primary lateral sclerosisErica Scirocco, Matti D Allen, Elisa Giacomelli, et al.
Human Mutation|July 17, 2013
Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12Guida Landouré, Peng-Peng Zhu, Charles M Lourenço, et al.
Pageof 37