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S Pack

Showing results (41-50 of 66) with videos related to

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Leukemia|February 12, 1999
Allelic loss of 11q13 as detected by MEN1-FISH is not associated with mutation of the MEN1 gene in lymphoid neoplasmsC Thieblemont, S Pack, A Sakai, et al.
Neuropathology and Applied Neurobiology|July 1, 1980
Immunogenetic studies of multiple sclerosis patients in Caithness County, ScotlandP Robertson, P Ward, J Brostoff, et al.
Human Genetics|November 3, 1998
In silico-initiated cloning and molecular characterization of a novel human member of the L1 gene family of neural cell adhesion moleculesM H Wei, I Karavanova, S V Ivanov, et al.
Biochimica Et Biophysica Acta|April 20, 2001
VAM-1: a new member of the MAGUK family binds to human Veli-1 through a conserved domainT C Tseng, S M Marfatia, P J Bryant, et al.
The Journal of Clinical Endocrinology and Metabolism|November 30, 2000
Ovarian lesions in Carney complex: clinical genetics and possible predisposition to malignancyC A Stratakis, T Papageorgiou, A Premkumar, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 24, 1998
11q13 allelic loss in pituitary tumors in patients with multiple endocrine neoplasia syndrome type 1R J Weil, A O Vortmeyer, S Huang, et al.
The American Journal of Pathology|August 6, 1999
Hereditary and sporadic papillary renal carcinomas with c-met mutations share a distinct morphological phenotypeI A Lubensky, L Schmidt, Z Zhuang, et al.
Journal of Medical Genetics|April 5, 2003
Chromosome 2 (2p16) abnormalities in Carney complex tumoursL Matyakhina, S Pack, L S Kirschner, et al.
The American Journal of Pathology|July 17, 1998
Multiple neuroendocrine tumors of the pancreas in von Hippel-Lindau disease patients: histopathological and molecular genetic analysisI A Lubensky, S Pack, D Ault, et al.
Human Mutation|November 26, 1998
Improved detection of germline mutations in the von Hippel-Lindau disease tumor suppressor geneC Stolle, G Glenn, B Zbar, et al.
Pageof 7

Showing results (41-50 of 66) with videos related to

Sort By:
Pageof 7
Leukemia|February 12, 1999
Allelic loss of 11q13 as detected by MEN1-FISH is not associated with mutation of the MEN1 gene in lymphoid neoplasmsC Thieblemont, S Pack, A Sakai, et al.
Neuropathology and Applied Neurobiology|July 1, 1980
Immunogenetic studies of multiple sclerosis patients in Caithness County, ScotlandP Robertson, P Ward, J Brostoff, et al.
Human Genetics|November 3, 1998
In silico-initiated cloning and molecular characterization of a novel human member of the L1 gene family of neural cell adhesion moleculesM H Wei, I Karavanova, S V Ivanov, et al.
Biochimica Et Biophysica Acta|April 20, 2001
VAM-1: a new member of the MAGUK family binds to human Veli-1 through a conserved domainT C Tseng, S M Marfatia, P J Bryant, et al.
The Journal of Clinical Endocrinology and Metabolism|November 30, 2000
Ovarian lesions in Carney complex: clinical genetics and possible predisposition to malignancyC A Stratakis, T Papageorgiou, A Premkumar, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 24, 1998
11q13 allelic loss in pituitary tumors in patients with multiple endocrine neoplasia syndrome type 1R J Weil, A O Vortmeyer, S Huang, et al.
The American Journal of Pathology|August 6, 1999
Hereditary and sporadic papillary renal carcinomas with c-met mutations share a distinct morphological phenotypeI A Lubensky, L Schmidt, Z Zhuang, et al.
Journal of Medical Genetics|April 5, 2003
Chromosome 2 (2p16) abnormalities in Carney complex tumoursL Matyakhina, S Pack, L S Kirschner, et al.
The American Journal of Pathology|July 17, 1998
Multiple neuroendocrine tumors of the pancreas in von Hippel-Lindau disease patients: histopathological and molecular genetic analysisI A Lubensky, S Pack, D Ault, et al.
Human Mutation|November 26, 1998
Improved detection of germline mutations in the von Hippel-Lindau disease tumor suppressor geneC Stolle, G Glenn, B Zbar, et al.
Pageof 7