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K Neale

Showing results (31-40 of 40) with videos related to

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Gut|August 14, 1999
Screening SMAD1, SMAD2, SMAD3, and SMAD5 for germline mutations in juvenile polyposis syndromeS Bevan, K Woodford-Richens, P Rozen, et al.
Human Molecular Genetics|January 15, 1999
Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancerA Ylikorkala, E Avizienyte, I P Tomlinson, et al.
Human Molecular Genetics|November 13, 1998
Mutations in DPC4 (SMAD4) cause juvenile polyposis syndrome, but only account for a minority of casesR Houlston, S Bevan, A Williams, et al.
Journal of Medical Genetics|February 25, 1998
Peutz-Jeghers disease: most, but not all, families are compatible with linkage to 19p13.3S Olschwang, D Markie, S Seal, et al.
Gut|February 8, 2006
Disease severity and genetic pathways in attenuated familial adenomatous polyposis vary greatly but depend on the site of the germline mutationO M Sieber, S Segditsas, A L Knudsen, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 28, 2002
Whole-gene APC deletions cause classical familial adenomatous polyposis, but not attenuated polyposis or "multiple" colorectal adenomasO M Sieber, H Lamlum, M D Crabtree, et al.
Cancer Research|November 26, 1997
Exclusion of PTEN and 10q22-24 as the susceptibility locus for juvenile polyposis syndromeD J Marsh, S Roth, K L Lunetta, et al.
British Journal of Cancer|July 17, 2003
Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndromeW Lim, N Hearle, B Shah, et al.
Gut|April 15, 2000
Analysis of genetic and phenotypic heterogeneity in juvenile polyposisK Woodford-Richens, S Bevan, M Churchman, et al.
American Journal of Human Genetics|September 6, 2001
Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromesX P Zhou, K Woodford-Richens, R Lehtonen, et al.
Pageof 4

Showing results (31-40 of 40) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
Gut|August 14, 1999
Screening SMAD1, SMAD2, SMAD3, and SMAD5 for germline mutations in juvenile polyposis syndromeS Bevan, K Woodford-Richens, P Rozen, et al.
Human Molecular Genetics|January 15, 1999
Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancerA Ylikorkala, E Avizienyte, I P Tomlinson, et al.
Human Molecular Genetics|November 13, 1998
Mutations in DPC4 (SMAD4) cause juvenile polyposis syndrome, but only account for a minority of casesR Houlston, S Bevan, A Williams, et al.
Journal of Medical Genetics|February 25, 1998
Peutz-Jeghers disease: most, but not all, families are compatible with linkage to 19p13.3S Olschwang, D Markie, S Seal, et al.
Gut|February 8, 2006
Disease severity and genetic pathways in attenuated familial adenomatous polyposis vary greatly but depend on the site of the germline mutationO M Sieber, S Segditsas, A L Knudsen, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 28, 2002
Whole-gene APC deletions cause classical familial adenomatous polyposis, but not attenuated polyposis or "multiple" colorectal adenomasO M Sieber, H Lamlum, M D Crabtree, et al.
Cancer Research|November 26, 1997
Exclusion of PTEN and 10q22-24 as the susceptibility locus for juvenile polyposis syndromeD J Marsh, S Roth, K L Lunetta, et al.
British Journal of Cancer|July 17, 2003
Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndromeW Lim, N Hearle, B Shah, et al.
Gut|April 15, 2000
Analysis of genetic and phenotypic heterogeneity in juvenile polyposisK Woodford-Richens, S Bevan, M Churchman, et al.
American Journal of Human Genetics|September 6, 2001
Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromesX P Zhou, K Woodford-Richens, R Lehtonen, et al.
Pageof 4