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N Katsanis

Showing results (1-10 of 29) with videos related to

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Cellular and Molecular Life Sciences : CMLS|June 1, 2005
Microtubule transport defects in neurological and ciliary diseaseJ M Gerdes, N Katsanis
Genomics|February 28, 1998
A novel C-terminal binding protein (CTBP2) is closely related to CTBP1, an adenovirus E1A-binding protein, and maps to human chromosome 21q21.3N Katsanis, E M Fisher
Human Genetics|October 1, 1996
The gene encoding the p60 subunit of chromatin assembly factor I (CAF1P60) maps to human chromosome 21q22.2, a region associated with some of the major features of Down syndromeN Katsanis, E M Fisher
Genomics|August 7, 1998
Identification, expression, and chromosomal localization of ubiquitin conjugating enzyme 7 (UBE2G2), a human homologue of the Saccharomyces cerevisiae ubc7 geneN Katsanis, E M Fisher
Genomics|July 1, 1996
Paralogy mapping: identification of a region in the human MHC triplicated onto human chromosomes 1 and 9 allows the prediction and isolation of novel PBX and NOTCH lociN Katsanis, J Fitzgibbon, E M Fisher
Nature Genetics|August 31, 2001
An evaluation of the draft human genome sequenceN Katsanis, K C Worley, J R Lupski
Human Genetics|September 1, 1997
Mapping of a novel SH3 domain protein and two proteins of unknown function to human chromosome 21N Katsanis, J A Beck, E M Fisher
Human Molecular Genetics|October 24, 2001
Exploring the molecular basis of Bardet-Biedl syndromeN Katsanis, J R Lupski, P L Beales
Human Genetics|September 12, 2000
Isolation of a paralog of the Doyne honeycomb retinal dystrophy gene from the multiple retinopathy critical region on 11q13N Katsanis, S Venable, J R Smith, et al.
Clinical Chemistry|April 28, 2001
New polymorphic short tandem repeats for PCR-based Charcot-Marie-Tooth disease type 1A duplication diagnosisJ L Badano, K Inoue, N Katsanis, et al.
Pageof 3

Showing results (1-10 of 29) with videos related to

Sort By:
Pageof 3
Cellular and Molecular Life Sciences : CMLS|June 1, 2005
Microtubule transport defects in neurological and ciliary diseaseJ M Gerdes, N Katsanis
Genomics|February 28, 1998
A novel C-terminal binding protein (CTBP2) is closely related to CTBP1, an adenovirus E1A-binding protein, and maps to human chromosome 21q21.3N Katsanis, E M Fisher
Human Genetics|October 1, 1996
The gene encoding the p60 subunit of chromatin assembly factor I (CAF1P60) maps to human chromosome 21q22.2, a region associated with some of the major features of Down syndromeN Katsanis, E M Fisher
Genomics|August 7, 1998
Identification, expression, and chromosomal localization of ubiquitin conjugating enzyme 7 (UBE2G2), a human homologue of the Saccharomyces cerevisiae ubc7 geneN Katsanis, E M Fisher
Genomics|July 1, 1996
Paralogy mapping: identification of a region in the human MHC triplicated onto human chromosomes 1 and 9 allows the prediction and isolation of novel PBX and NOTCH lociN Katsanis, J Fitzgibbon, E M Fisher
Nature Genetics|August 31, 2001
An evaluation of the draft human genome sequenceN Katsanis, K C Worley, J R Lupski
Human Genetics|September 1, 1997
Mapping of a novel SH3 domain protein and two proteins of unknown function to human chromosome 21N Katsanis, J A Beck, E M Fisher
Human Molecular Genetics|October 24, 2001
Exploring the molecular basis of Bardet-Biedl syndromeN Katsanis, J R Lupski, P L Beales
Human Genetics|September 12, 2000
Isolation of a paralog of the Doyne honeycomb retinal dystrophy gene from the multiple retinopathy critical region on 11q13N Katsanis, S Venable, J R Smith, et al.
Clinical Chemistry|April 28, 2001
New polymorphic short tandem repeats for PCR-based Charcot-Marie-Tooth disease type 1A duplication diagnosisJ L Badano, K Inoue, N Katsanis, et al.
Pageof 3