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P Sistonen

Showing results (81-90 of 110) with videos related to

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Cancer Research|August 15, 1991
Evidence supporting exclusion of the DCC gene and a portion of chromosome 18q as the locus for susceptibility to hereditary nonpolyposis colorectal carcinoma in five kindredsP Peltomäki, P Sistonen, J P Mecklin, et al.
American Journal of Human Genetics|April 1, 1997
Assignment of the mulibrey nanism gene to 17q by linkage and linkage-disequilibrium analysisK Avela, M Lipsanen-Nyman, J Perheentupa, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in ScandinaviaJ Jonasson, V Juvonen, P Sistonen, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 21, 1994
Close linkage to chromosome 3p and conservation of ancestral founding haplotype in hereditary nonpolyposis colorectal cancer familiesM Nyström-Lahti, P Sistonen, J P Mecklin, et al.
The American Journal of Pathology|September 11, 2001
Familial cutaneous leiomyomatosis is a two-hit condition associated with renal cell cancer of characteristic histopathologyM Kiuru, V Launonen, M Hietala, et al.
Human Molecular Genetics|November 1, 1994
Three dinucleotide repeat polymorphisms proximal to the D2S123 locusF S Leach, N C Nicolaides, P Sistonen, et al.
Gut|June 22, 2002
Frequent loss of SMAD4/DPC4 protein in colorectal cancersR Salovaara, S Roth, A Loukola, et al.
Cell|December 17, 1993
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancerF S Leach, N C Nicolaides, N Papadopoulos, et al.
American Journal of Human Genetics|October 1, 1994
Mismatch repair genes on chromosomes 2p and 3p account for a major share of hereditary nonpolyposis colorectal cancer families evaluable by linkageM Nyström-Lahti, R Parsons, P Sistonen, et al.
Science (New York, N.Y.)|May 7, 1993
Clues to the pathogenesis of familial colorectal cancerL A Aaltonen, P Peltomäki, F S Leach, et al.
Pageof 11

Showing results (81-90 of 110) with videos related to

Sort By:
Pageof 11
Cancer Research|August 15, 1991
Evidence supporting exclusion of the DCC gene and a portion of chromosome 18q as the locus for susceptibility to hereditary nonpolyposis colorectal carcinoma in five kindredsP Peltomäki, P Sistonen, J P Mecklin, et al.
American Journal of Human Genetics|April 1, 1997
Assignment of the mulibrey nanism gene to 17q by linkage and linkage-disequilibrium analysisK Avela, M Lipsanen-Nyman, J Perheentupa, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in ScandinaviaJ Jonasson, V Juvonen, P Sistonen, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 21, 1994
Close linkage to chromosome 3p and conservation of ancestral founding haplotype in hereditary nonpolyposis colorectal cancer familiesM Nyström-Lahti, P Sistonen, J P Mecklin, et al.
The American Journal of Pathology|September 11, 2001
Familial cutaneous leiomyomatosis is a two-hit condition associated with renal cell cancer of characteristic histopathologyM Kiuru, V Launonen, M Hietala, et al.
Human Molecular Genetics|November 1, 1994
Three dinucleotide repeat polymorphisms proximal to the D2S123 locusF S Leach, N C Nicolaides, P Sistonen, et al.
Gut|June 22, 2002
Frequent loss of SMAD4/DPC4 protein in colorectal cancersR Salovaara, S Roth, A Loukola, et al.
Cell|December 17, 1993
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancerF S Leach, N C Nicolaides, N Papadopoulos, et al.
American Journal of Human Genetics|October 1, 1994
Mismatch repair genes on chromosomes 2p and 3p account for a major share of hereditary nonpolyposis colorectal cancer families evaluable by linkageM Nyström-Lahti, R Parsons, P Sistonen, et al.
Science (New York, N.Y.)|May 7, 1993
Clues to the pathogenesis of familial colorectal cancerL A Aaltonen, P Peltomäki, F S Leach, et al.
Pageof 11