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J Plaschke

Showing results (11-20 of 21) with videos related to

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Genetics|August 5, 1998
A microsatellite map of wheatM S Röder, V Korzun, K Wendehake, et al.
International Journal of Colorectal Disease|January 5, 2002
Combined molecular and clinical approach for decision making for surgery in HNPCC patients: a report on three cases in two familiesS R Pistorius, M Nagel, S Kruger, et al.
Molecular & General Genetics : MGG|February 6, 1995
Abundance, variability and chromosomal location of microsatellites in wheatM S Röder, J Plaschke, S U König, et al.
Cancer Research|July 1, 1997
The putative tumor suppressor gene FHIT at 3p14.2 is rarely affected by loss of heterozygosity in primary human brain tumorsS Frank, J Müller, J Plaschke, et al.
International Journal of Cancer|March 4, 2000
Sequence analysis of the mismatch repair gene hMSH6 in the germline of patients with familial and sporadic colorectal cancerJ Plaschke, C Kruppa, R Tischler, et al.
European Journal of Cancer (Oxford, England : 1990)|February 21, 1998
An intronic germline transition in the HNPCC gene hMSH2 is associated with sporadic colorectal cancerC Goessl, J Plaschke, S Pistorius, et al.
International Journal of Colorectal Disease|January 11, 2001
Clinical consequences of molecular diagnosis in families with mismatch repair gene germline mutationsS R Pistorius, C Kruppa, S Haas, et al.
Journal of Medical Genetics|October 4, 2005
The p53 codon 72 variation is associated with the age of onset of hereditary non-polyposis colorectal cancer (HNPCC)S Krüger, A Bier, C Engel, et al.
Der Pathologe|May 13, 2004
[Molecular pathology in hereditary colorectal cancer. Recommendations of the Collaborative German Study Group on hereditary colorectal cancer funded by the German Cancer Aid (Deutsche Krebshilfe)]J Rüschoff, B Roggendorf, F Brasch, et al.
Journal of Biochemical and Biophysical Methods|February 17, 2001
DHPLC mutation analysis of the hereditary nonpolyposis colon cancer (HNPCC) genes hMLH1 and hMSH2E Holinski-Feder, Y Müller-Koch, W Friedl, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Genetics|August 5, 1998
A microsatellite map of wheatM S Röder, V Korzun, K Wendehake, et al.
International Journal of Colorectal Disease|January 5, 2002
Combined molecular and clinical approach for decision making for surgery in HNPCC patients: a report on three cases in two familiesS R Pistorius, M Nagel, S Kruger, et al.
Molecular & General Genetics : MGG|February 6, 1995
Abundance, variability and chromosomal location of microsatellites in wheatM S Röder, J Plaschke, S U König, et al.
Cancer Research|July 1, 1997
The putative tumor suppressor gene FHIT at 3p14.2 is rarely affected by loss of heterozygosity in primary human brain tumorsS Frank, J Müller, J Plaschke, et al.
International Journal of Cancer|March 4, 2000
Sequence analysis of the mismatch repair gene hMSH6 in the germline of patients with familial and sporadic colorectal cancerJ Plaschke, C Kruppa, R Tischler, et al.
European Journal of Cancer (Oxford, England : 1990)|February 21, 1998
An intronic germline transition in the HNPCC gene hMSH2 is associated with sporadic colorectal cancerC Goessl, J Plaschke, S Pistorius, et al.
International Journal of Colorectal Disease|January 11, 2001
Clinical consequences of molecular diagnosis in families with mismatch repair gene germline mutationsS R Pistorius, C Kruppa, S Haas, et al.
Journal of Medical Genetics|October 4, 2005
The p53 codon 72 variation is associated with the age of onset of hereditary non-polyposis colorectal cancer (HNPCC)S Krüger, A Bier, C Engel, et al.
Der Pathologe|May 13, 2004
[Molecular pathology in hereditary colorectal cancer. Recommendations of the Collaborative German Study Group on hereditary colorectal cancer funded by the German Cancer Aid (Deutsche Krebshilfe)]J Rüschoff, B Roggendorf, F Brasch, et al.
Journal of Biochemical and Biophysical Methods|February 17, 2001
DHPLC mutation analysis of the hereditary nonpolyposis colon cancer (HNPCC) genes hMLH1 and hMSH2E Holinski-Feder, Y Müller-Koch, W Friedl, et al.
Pageof 3