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K-H Grzeschik

Showing results (51-60 of 162) with videos related to

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Human Genetics|December 1, 1989
The gene encoding the human preproacrosin (ACR) maps to the q13-qter region on chromosome 22I M Adham, K H Grzeschik, A H Geurts van Kessel, et al.
The Journal of Biological Chemistry|October 5, 1989
Cytovillin, a microvillar Mr 75,000 protein. cDNA sequence, prokaryotic expression, and chromosomal localizationO Turunen, R Winqvist, R Pakkanen, et al.
American Journal of Medical Genetics|March 4, 2000
Boy with syndactylies, macrocephaly, and severe skeletal dysplasia: not a new syndrome, but two dominant mutations (GLI3 E543X and COL2A1 G973R) in the same individualD Sobetzko, G Eich, M Kalff-Suske, et al.
European Journal of Biochemistry|July 1, 1989
The human lysozyme gene. Sequence organization and chromosomal localizationC W Peters, U Kruse, R Pollwein, et al.
Annales De Genetique|January 1, 1980
Assignment of the gene coding for human catalase to the short arm of chromosome 11P Wieacker, C R Mueller, A Mayerova, et al.
Cell Motility and the Cytoskeleton|November 15, 2007
Novel interaction partners of Bardet-Biedl syndrome proteinsF Oeffner, C Moch, A Neundorf, et al.
Human Genetics|June 1, 1992
Simple repeat sequences on the human Y chromosome are equally polymorphic as their autosomal counterpartsL Roewer, J Arnemann, N K Spurr, et al.
Human Genetics|October 1, 1990
The gene for 17 beta-hydroxysteroid dehydrogenase maps to human chromosome 17, bands q12-q21, and shows an RFLP with ScaIR Winqvist, H Peltoketo, V Isomaa, et al.
American Journal of Medical Genetics|November 1, 1988
Two mosaic cases with nonfluorescent Y chromosome analysed with Y-specific DNA probesB Kałuzewski, L Jakubowski, M Debiec-Rychter, et al.
Oncogene|December 1, 1991
Evidence for human DNA-mediated transfer of the suppressed phenotype into malignant Chinese hamster cellsR Schäfer, A C Nirkko, P M Ambühl, et al.
Pageof 17

Showing results (51-60 of 162) with videos related to

Sort By:
Pageof 17
Human Genetics|December 1, 1989
The gene encoding the human preproacrosin (ACR) maps to the q13-qter region on chromosome 22I M Adham, K H Grzeschik, A H Geurts van Kessel, et al.
The Journal of Biological Chemistry|October 5, 1989
Cytovillin, a microvillar Mr 75,000 protein. cDNA sequence, prokaryotic expression, and chromosomal localizationO Turunen, R Winqvist, R Pakkanen, et al.
American Journal of Medical Genetics|March 4, 2000
Boy with syndactylies, macrocephaly, and severe skeletal dysplasia: not a new syndrome, but two dominant mutations (GLI3 E543X and COL2A1 G973R) in the same individualD Sobetzko, G Eich, M Kalff-Suske, et al.
European Journal of Biochemistry|July 1, 1989
The human lysozyme gene. Sequence organization and chromosomal localizationC W Peters, U Kruse, R Pollwein, et al.
Annales De Genetique|January 1, 1980
Assignment of the gene coding for human catalase to the short arm of chromosome 11P Wieacker, C R Mueller, A Mayerova, et al.
Cell Motility and the Cytoskeleton|November 15, 2007
Novel interaction partners of Bardet-Biedl syndrome proteinsF Oeffner, C Moch, A Neundorf, et al.
Human Genetics|June 1, 1992
Simple repeat sequences on the human Y chromosome are equally polymorphic as their autosomal counterpartsL Roewer, J Arnemann, N K Spurr, et al.
Human Genetics|October 1, 1990
The gene for 17 beta-hydroxysteroid dehydrogenase maps to human chromosome 17, bands q12-q21, and shows an RFLP with ScaIR Winqvist, H Peltoketo, V Isomaa, et al.
American Journal of Medical Genetics|November 1, 1988
Two mosaic cases with nonfluorescent Y chromosome analysed with Y-specific DNA probesB Kałuzewski, L Jakubowski, M Debiec-Rychter, et al.
Oncogene|December 1, 1991
Evidence for human DNA-mediated transfer of the suppressed phenotype into malignant Chinese hamster cellsR Schäfer, A C Nirkko, P M Ambühl, et al.
Pageof 17