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P Kioschis

Showing results (31-40 of 37) with videos related to

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Genomics|July 15, 1996
The genomic organization of a human creatine transporter (CRTR) gene located in Xq28N Sandoval, D Bauer, V Brenner, et al.
Genomics|May 1, 1996
A 900-kb cosmid contig and 10 new transcripts within the candidate region for myotubular myopathy (MTM1)P Kioschis, U C Rogner, E Pick, et al.
Human Molecular Genetics|January 1, 1996
Deletions in Xq28 in two boys with myotubular myopathy and abnormal genital development define a new contiguous gene syndrome in a 430 kb regionL J Hu, J Laporte, W Kress, et al.
Genomics|November 26, 1998
Genomic organization of a 225-kb region in Xq28 containing the gene for X-linked myotubular myopathy (MTM1) and a related gene (MTMR1)P Kioschis, S Wiemann, N S Heiss, et al.
Human Molecular Genetics|February 13, 2001
A translocation breakpoint cluster disrupts the newly defined 3' end of the SNURF-SNRPN transcription unit on chromosome 15J Wirth, E Back, A Hüttenhofer, et al.
Nature|June 6, 2000
Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) ConsortiumA Smahi, G Courtois, P Vabres, et al.
Genome Research|June 16, 2000
Comparative genome sequence analysis of the Bpa/Str region in mouse and ManA M Mallon, M Platzer, R Bate, et al.
Pageof 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Genomics|July 15, 1996
The genomic organization of a human creatine transporter (CRTR) gene located in Xq28N Sandoval, D Bauer, V Brenner, et al.
Genomics|May 1, 1996
A 900-kb cosmid contig and 10 new transcripts within the candidate region for myotubular myopathy (MTM1)P Kioschis, U C Rogner, E Pick, et al.
Human Molecular Genetics|January 1, 1996
Deletions in Xq28 in two boys with myotubular myopathy and abnormal genital development define a new contiguous gene syndrome in a 430 kb regionL J Hu, J Laporte, W Kress, et al.
Genomics|November 26, 1998
Genomic organization of a 225-kb region in Xq28 containing the gene for X-linked myotubular myopathy (MTM1) and a related gene (MTMR1)P Kioschis, S Wiemann, N S Heiss, et al.
Human Molecular Genetics|February 13, 2001
A translocation breakpoint cluster disrupts the newly defined 3' end of the SNURF-SNRPN transcription unit on chromosome 15J Wirth, E Back, A Hüttenhofer, et al.
Nature|June 6, 2000
Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) ConsortiumA Smahi, G Courtois, P Vabres, et al.
Genome Research|June 16, 2000
Comparative genome sequence analysis of the Bpa/Str region in mouse and ManA M Mallon, M Platzer, R Bate, et al.
Pageof 4