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H G Nothwang

Showing results (21-30 of 32) with videos related to

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FEBS Letters|March 23, 1992
Structure and RNA content of the prosomesO Coux, H G Nothwang, K Scherrer, et al.
Science (New York, N.Y.)|August 26, 1994
cDNA cloning and interferon gamma down-regulation of proteasomal subunits X and YK Akiyama, K Yokota, S Kagawa, et al.
HNO|April 10, 2019
[Scanning laser optical tomography in a neuropathic mouse model : Visualization of structural changes. German version]J Schulze, L Nolte, S Lyutenski, et al.
HNO|May 9, 2019
Scanning laser optical tomography in a neuropathic mouse model : Visualization of structural changesJ Schulze, L Nolte, S Lyutenski, et al.
Pediatric Nephrology (Berlin, Germany)|March 21, 1998
Lack of large, homozygous deletions of the nephronophthisis 1 region in Joubert syndrome type B. APN Study Group. Arbeitsgemeinschaft für Pädiatrische NephrologieF Hildebrandt, H G Nothwang, U Vossmerbäumer, et al.
Genomics|May 1, 1997
Molecular cloning of the interleukin-1 gene cluster: construction of an integrated YAC/PAC contig and a partial transcriptional map in the region of chromosome 2q13H G Nothwang, B Strahm, D Denich, et al.
Journal of Medical Genetics|May 5, 1999
Systematic characterisation of disease associated balanced chromosome rearrangements by FISH: cytogenetically and genetically anchored YACs identify microdeletions and candidate regions for mental retardation genesJ Wirth, H G Nothwang, S van der Maarel, 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 Genetics|January 4, 2001
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1DH Bolz, B von Brederlow, A Ramírez, et al.
Cytogenetics and Cell Genetics|November 4, 2000
Molecular cloning of Xp11 breakpoints in two unrelated mentally retarded females with X;autosome translocationsH G Nothwang, A Schröer, S van der Maarel, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
FEBS Letters|March 23, 1992
Structure and RNA content of the prosomesO Coux, H G Nothwang, K Scherrer, et al.
Science (New York, N.Y.)|August 26, 1994
cDNA cloning and interferon gamma down-regulation of proteasomal subunits X and YK Akiyama, K Yokota, S Kagawa, et al.
HNO|April 10, 2019
[Scanning laser optical tomography in a neuropathic mouse model : Visualization of structural changes. German version]J Schulze, L Nolte, S Lyutenski, et al.
HNO|May 9, 2019
Scanning laser optical tomography in a neuropathic mouse model : Visualization of structural changesJ Schulze, L Nolte, S Lyutenski, et al.
Pediatric Nephrology (Berlin, Germany)|March 21, 1998
Lack of large, homozygous deletions of the nephronophthisis 1 region in Joubert syndrome type B. APN Study Group. Arbeitsgemeinschaft für Pädiatrische NephrologieF Hildebrandt, H G Nothwang, U Vossmerbäumer, et al.
Genomics|May 1, 1997
Molecular cloning of the interleukin-1 gene cluster: construction of an integrated YAC/PAC contig and a partial transcriptional map in the region of chromosome 2q13H G Nothwang, B Strahm, D Denich, et al.
Journal of Medical Genetics|May 5, 1999
Systematic characterisation of disease associated balanced chromosome rearrangements by FISH: cytogenetically and genetically anchored YACs identify microdeletions and candidate regions for mental retardation genesJ Wirth, H G Nothwang, S van der Maarel, 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 Genetics|January 4, 2001
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1DH Bolz, B von Brederlow, A Ramírez, et al.
Cytogenetics and Cell Genetics|November 4, 2000
Molecular cloning of Xp11 breakpoints in two unrelated mentally retarded females with X;autosome translocationsH G Nothwang, A Schröer, S van der Maarel, et al.
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