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M Linehan

Showing results (411-420 of 443) with videos related to

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Cancer Research|February 11, 1998
Loss of heterozygosity and somatic mutations of the VHL tumor suppressor gene in sporadic cerebellar hemangioblastomasJ Y Lee, S M Dong, W S Park, et al.
Journal of Medical Genetics|February 1, 2008
BHD mutations, clinical and molecular genetic investigations of Birt-Hogg-Dubé syndrome: a new series of 50 families and a review of published reportsJ R Toro, M-H Wei, G M Glenn, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 11, 2026
Strain-specific propagation of variant Creutzfeldt-Jakob disease prions in humanized neural cellsMelissa L D Rayner, Parineeta Arora, Jacqueline M Linehan, et al.
Cancer Research|November 24, 2001
The consequences of chromosomal aneuploidy on gene expression profiles in a cell line model for prostate carcinogenesisJ L Phillips, S W Hayward, Y Wang, et al.
Urology|August 1, 1997
Phase I trial of photodynamic therapy in the treatment of recurrent superficial transitional cell carcinoma of the bladderM M Walther, T F Delaney, P D Smith, et al.
Plos Pathogens|February 20, 2025
Isolation of a novel human prion strain from a PRNP codon 129 heterozygous vCJD patientFuquan Zhang, Susan Joiner, Jacqueline M Linehan, et al.
Journal of Medical Genetics|June 7, 2005
Novel mutations in FH and expansion of the spectrum of phenotypes expressed in families with hereditary leiomyomatosis and renal cell cancerM-H Wei, O Toure, G M Glenn, et al.
Nature|June 11, 2015
A naturally occurring variant of the human prion protein completely prevents prion diseaseEmmanuel A Asante, Michelle Smidak, Andrew Grimshaw, et al.
Oncogene|May 24, 2011
Inactivation of the von Hippel-Lindau tumor suppressor leads to selective expression of a human endogenous retrovirus in kidney cancerE Cherkasova, E Malinzak, S Rao, et al.
American Journal of Human Genetics|September 5, 2001
Birt-Hogg-Dubé syndrome, a genodermatosis associated with spontaneous pneumothorax and kidney neoplasia, maps to chromosome 17p11.2L S Schmidt, M B Warren, M L Nickerson, et al.
Pageof 45

Showing results (411-420 of 443) with videos related to

Sort By:
Pageof 45
Cancer Research|February 11, 1998
Loss of heterozygosity and somatic mutations of the VHL tumor suppressor gene in sporadic cerebellar hemangioblastomasJ Y Lee, S M Dong, W S Park, et al.
Journal of Medical Genetics|February 1, 2008
BHD mutations, clinical and molecular genetic investigations of Birt-Hogg-Dubé syndrome: a new series of 50 families and a review of published reportsJ R Toro, M-H Wei, G M Glenn, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 11, 2026
Strain-specific propagation of variant Creutzfeldt-Jakob disease prions in humanized neural cellsMelissa L D Rayner, Parineeta Arora, Jacqueline M Linehan, et al.
Cancer Research|November 24, 2001
The consequences of chromosomal aneuploidy on gene expression profiles in a cell line model for prostate carcinogenesisJ L Phillips, S W Hayward, Y Wang, et al.
Urology|August 1, 1997
Phase I trial of photodynamic therapy in the treatment of recurrent superficial transitional cell carcinoma of the bladderM M Walther, T F Delaney, P D Smith, et al.
Plos Pathogens|February 20, 2025
Isolation of a novel human prion strain from a PRNP codon 129 heterozygous vCJD patientFuquan Zhang, Susan Joiner, Jacqueline M Linehan, et al.
Journal of Medical Genetics|June 7, 2005
Novel mutations in FH and expansion of the spectrum of phenotypes expressed in families with hereditary leiomyomatosis and renal cell cancerM-H Wei, O Toure, G M Glenn, et al.
Nature|June 11, 2015
A naturally occurring variant of the human prion protein completely prevents prion diseaseEmmanuel A Asante, Michelle Smidak, Andrew Grimshaw, et al.
Oncogene|May 24, 2011
Inactivation of the von Hippel-Lindau tumor suppressor leads to selective expression of a human endogenous retrovirus in kidney cancerE Cherkasova, E Malinzak, S Rao, et al.
American Journal of Human Genetics|September 5, 2001
Birt-Hogg-Dubé syndrome, a genodermatosis associated with spontaneous pneumothorax and kidney neoplasia, maps to chromosome 17p11.2L S Schmidt, M B Warren, M L Nickerson, et al.
Pageof 45