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Showing results (71-80 of 150) with videos related to

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Mechanisms of Development|September 24, 1999
Dickkopf genes are co-ordinately expressed in mesodermal lineagesA P Monaghan, P Kioschis, W Wu, et al.
Genetic Counseling (Geneva, Switzerland)|August 9, 2001
One novel and two recurrent missense DKC1 mutations in patients with dyskeratosis congenita (DKC)N S Heiss, A Mégarbané, S M Klauck, et al.
Human Molecular Genetics|November 1, 1994
Rapid identification of gene sequences for transcriptional map assembly by direct cDNA screening of genomic reference librariesB J Lawrence, W Schwabe, P Kioschis, et al.
Molecular Psychiatry|July 1, 1996
Point mutation analysis of the FMR-1 gene in autismJ B Vincent, D S Konecki, E Munstermann, et al.
Gene|June 19, 2001
RAI1 is a novel polyglutamine encoding gene that is deleted in Smith-Magenis syndrome patientsP Seranski, C Hoff, U Radelof, et al.
Verhandlungen Der Deutschen Gesellschaft Fur Pathologie|March 22, 2003
Transcription profiling of renal cell carcinomaW Huber, J M Boer, A von Heydebreck, et al.
Nature Genetics|September 1, 1997
DMBT1, a new member of the SRCR superfamily, on chromosome 10q25.3-26.1 is deleted in malignant brain tumoursJ Mollenhauer, S Wiemann, W Scheurlen, et al.
Human Genetics|August 1, 1996
X-linked myotubular myopathy: refinement of the gene to a 280-kb region with new and highly informative microsatellite markersL J Hu, J Laporte, P Kioschis, et al.
The Journal of Biological Chemistry|July 25, 1998
The human glycine receptor subunit alpha3. Glra3 gene structure, chromosomal localization, and functional characterization of alternative transcriptsZ Nikolic, B Laube, R G Weber, et al.
Genomics|July 1, 1994
Genomic organization of the adrenoleukodystrophy geneC O Sarde, J Mosser, P Kioschis, et al.
Pageof 15

Showing results (71-80 of 150) with videos related to

Sort By:
Pageof 15
Mechanisms of Development|September 24, 1999
Dickkopf genes are co-ordinately expressed in mesodermal lineagesA P Monaghan, P Kioschis, W Wu, et al.
Genetic Counseling (Geneva, Switzerland)|August 9, 2001
One novel and two recurrent missense DKC1 mutations in patients with dyskeratosis congenita (DKC)N S Heiss, A Mégarbané, S M Klauck, et al.
Human Molecular Genetics|November 1, 1994
Rapid identification of gene sequences for transcriptional map assembly by direct cDNA screening of genomic reference librariesB J Lawrence, W Schwabe, P Kioschis, et al.
Molecular Psychiatry|July 1, 1996
Point mutation analysis of the FMR-1 gene in autismJ B Vincent, D S Konecki, E Munstermann, et al.
Gene|June 19, 2001
RAI1 is a novel polyglutamine encoding gene that is deleted in Smith-Magenis syndrome patientsP Seranski, C Hoff, U Radelof, et al.
Verhandlungen Der Deutschen Gesellschaft Fur Pathologie|March 22, 2003
Transcription profiling of renal cell carcinomaW Huber, J M Boer, A von Heydebreck, et al.
Nature Genetics|September 1, 1997
DMBT1, a new member of the SRCR superfamily, on chromosome 10q25.3-26.1 is deleted in malignant brain tumoursJ Mollenhauer, S Wiemann, W Scheurlen, et al.
Human Genetics|August 1, 1996
X-linked myotubular myopathy: refinement of the gene to a 280-kb region with new and highly informative microsatellite markersL J Hu, J Laporte, P Kioschis, et al.
The Journal of Biological Chemistry|July 25, 1998
The human glycine receptor subunit alpha3. Glra3 gene structure, chromosomal localization, and functional characterization of alternative transcriptsZ Nikolic, B Laube, R G Weber, et al.
Genomics|July 1, 1994
Genomic organization of the adrenoleukodystrophy geneC O Sarde, J Mosser, P Kioschis, et al.
Pageof 15