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K Tory

Showing results (51-60 of 57) with videos related to

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Journal of Medical Genetics|February 1, 1993
Detailed genetic mapping of the von Hippel-Lindau disease tumour suppressor geneF M Richards, E R Maher, F Latif, et al.
Human Genetics|January 1, 1994
Molecular genetic investigations of the mechanism of tumourigenesis in von Hippel-Lindau disease: analysis of allele loss in VHL tumoursP A Crossey, K Foster, F M Richards, et al.
Human Molecular Genetics|March 1, 1993
Genetic linkage between von Hippel-Lindau disease and three microsatellite polymorphisms refines the localisation of the VHL locusP A Crossey, E R Maher, M H Jones, et al.
Genes, Chromosomes & Cancer|September 1, 1992
Molecular characterization of a large homozygous deletion in the small cell lung cancer cell line U2020: a strategy for cloning the putative tumor suppressor geneF Latif, K Tory, W S Modi, et al.
FEBS Letters|January 15, 1998
NotI linking/jumping clones of human chromosome 3: mapping of the TFRC, RAB7 and HAUSP genes to regions rearranged in leukemia and deleted in solid tumorsV I Kashuba, R Z Gizatullin, A I Protopopov, et al.
Journal of Medical Genetics|June 11, 2009
Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11)E A Otto, K Tory, M Attanasio, et al.
Acta Ophthalmologica|February 3, 2026
Aniridia-associated keratopathy: Clinical and molecular mechanisms of disease progression and emerging therapeutic targetsN Szentmáry, S Suiwal, M Amini, et al.
Pageof 6

Showing results (51-60 of 57) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 57 results.
Journal of Medical Genetics|February 1, 1993
Detailed genetic mapping of the von Hippel-Lindau disease tumour suppressor geneF M Richards, E R Maher, F Latif, et al.
Human Genetics|January 1, 1994
Molecular genetic investigations of the mechanism of tumourigenesis in von Hippel-Lindau disease: analysis of allele loss in VHL tumoursP A Crossey, K Foster, F M Richards, et al.
Human Molecular Genetics|March 1, 1993
Genetic linkage between von Hippel-Lindau disease and three microsatellite polymorphisms refines the localisation of the VHL locusP A Crossey, E R Maher, M H Jones, et al.
Genes, Chromosomes & Cancer|September 1, 1992
Molecular characterization of a large homozygous deletion in the small cell lung cancer cell line U2020: a strategy for cloning the putative tumor suppressor geneF Latif, K Tory, W S Modi, et al.
FEBS Letters|January 15, 1998
NotI linking/jumping clones of human chromosome 3: mapping of the TFRC, RAB7 and HAUSP genes to regions rearranged in leukemia and deleted in solid tumorsV I Kashuba, R Z Gizatullin, A I Protopopov, et al.
Journal of Medical Genetics|June 11, 2009
Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11)E A Otto, K Tory, M Attanasio, et al.
Acta Ophthalmologica|February 3, 2026
Aniridia-associated keratopathy: Clinical and molecular mechanisms of disease progression and emerging therapeutic targetsN Szentmáry, S Suiwal, M Amini, et al.
Pageof 6