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W G Ballhausen

Showing results (11-20 of 35) with videos related to

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International Journal of Cancer|November 3, 1995
Multiple APC messenger RNA isoforms encoding exon 15 short open reading frames are expressed in the context of a novel exon 10A-derived sequenceZ Sulekova, J Reina-Sanchez, W G Ballhausen
Gastroenterology|March 1, 1997
Childhood hepatocellular adenoma in familial adenomatous polyposis: mutations in adenomatous polyposis coli gene and p53S Bala, P H Wünsch, W G Ballhausen
Human Genetics|October 1, 1996
Mosaicism of a microdeletion of 486 bp involving the CGG repeat of the FMR1 gene due to misalignment of GTT tandem repeats at chi-like elements flanking both breakpoints and a full mutationB Schmucker, W G Ballhausen, R A Pfeiffer
Anticancer Research|March 1, 1992
The human lck cDNA clone YT16 is a transforming oncogeneK M Mayer, I J Ansotegui, W G Ballhausen
Biochimica Et Biophysica Acta|August 22, 1995
The human high mobility group (HMG)-box transcription factor TCF-1: novel isoforms due to alternative splicing and usage of a new exon IXAK Mayer, E Wolff, H Clevers, et al.
International Journal of Cancer|January 26, 1996
Immunochemical identification of novel high-molecular-weight protein isoforms of the adenomatous polyposis coli (APC) geneC Kraus, J Reina-Sanchez, Z Suleková, et al.
Anticancer Research|May 5, 1999
Exon 14-skipping of the adenomatous polyposis coli gene in purified epithelial cells of colonic mucosa and tumorsZ Sulekova, M Reymond, F Köckerling, et al.
Human Genetics|August 1, 1991
Detection of APC region-specific signals by nonisotopic chromosomal in situ suppression (CISS)-hybridization using a microdissection library as a probeU Trautmann, G Leuteritz, G Senger, et al.
Der Chirurg; Zeitschrift Fur Alle Gebiete Der Operativen Medizen|June 7, 2000
[Hereditary colonic carcinoma without polyposis (HNPCC) without satisfying the Amsterdam criteria]S Kastl, K Günther, S Merkel, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
RNA-based mutation screening in German families with Sjögren-Larsson syndromeC Kraus, C Braun-Quentin, W G Ballhausen, et al.
Pageof 4

Showing results (11-20 of 35) with videos related to

Sort By:
Pageof 4
International Journal of Cancer|November 3, 1995
Multiple APC messenger RNA isoforms encoding exon 15 short open reading frames are expressed in the context of a novel exon 10A-derived sequenceZ Sulekova, J Reina-Sanchez, W G Ballhausen
Gastroenterology|March 1, 1997
Childhood hepatocellular adenoma in familial adenomatous polyposis: mutations in adenomatous polyposis coli gene and p53S Bala, P H Wünsch, W G Ballhausen
Human Genetics|October 1, 1996
Mosaicism of a microdeletion of 486 bp involving the CGG repeat of the FMR1 gene due to misalignment of GTT tandem repeats at chi-like elements flanking both breakpoints and a full mutationB Schmucker, W G Ballhausen, R A Pfeiffer
Anticancer Research|March 1, 1992
The human lck cDNA clone YT16 is a transforming oncogeneK M Mayer, I J Ansotegui, W G Ballhausen
Biochimica Et Biophysica Acta|August 22, 1995
The human high mobility group (HMG)-box transcription factor TCF-1: novel isoforms due to alternative splicing and usage of a new exon IXAK Mayer, E Wolff, H Clevers, et al.
International Journal of Cancer|January 26, 1996
Immunochemical identification of novel high-molecular-weight protein isoforms of the adenomatous polyposis coli (APC) geneC Kraus, J Reina-Sanchez, Z Suleková, et al.
Anticancer Research|May 5, 1999
Exon 14-skipping of the adenomatous polyposis coli gene in purified epithelial cells of colonic mucosa and tumorsZ Sulekova, M Reymond, F Köckerling, et al.
Human Genetics|August 1, 1991
Detection of APC region-specific signals by nonisotopic chromosomal in situ suppression (CISS)-hybridization using a microdissection library as a probeU Trautmann, G Leuteritz, G Senger, et al.
Der Chirurg; Zeitschrift Fur Alle Gebiete Der Operativen Medizen|June 7, 2000
[Hereditary colonic carcinoma without polyposis (HNPCC) without satisfying the Amsterdam criteria]S Kastl, K Günther, S Merkel, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
RNA-based mutation screening in German families with Sjögren-Larsson syndromeC Kraus, C Braun-Quentin, W G Ballhausen, et al.
Pageof 4