Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

J W Touchman

Showing results (1-10 of 17) with videos related to

Pageof 2
Sort By:
Genome Research|February 19, 1999
An effective approach for analyzing "prefinished" genomic sequence dataP M Kuehl, J M Weisemann, J W Touchman, et al.
Blood|February 9, 2000
Analysis of expressed immunoglobulin heavy chain genes in familial B-CLLA Sakai, G E Marti, N Caporaso, et al.
Journal of Virology|December 1, 1995
Branchpoint and polypyrimidine tract mutations mediating the loss and partial recovery of the Moloney murine sarcoma virus MuSVts110 thermosensitive splicing phenotypeJ W Touchman, I D'Souza, C A Heckman, et al.
Molecular Genetics and Metabolism|March 9, 1999
Identification and detection of the common 65-kb deletion breakpoint in the nephropathic cystinosis gene (CTNS)Y Anikster, C Lucero, J W Touchman, et al.
Genome Research|January 13, 2001
Human and mouse alpha-synuclein genes: comparative genomic sequence analysis and identification of a novel gene regulatory elementJ W Touchman, A Dehejia, O Chiba-Falek, et al.
Genome Research|March 1, 1997
2006 expressed-sequence tags derived from human chromosome 7-enriched cDNA librariesJ W Touchman, G G Bouffard, L A Weintraub, et al.
Genome Research|February 15, 2000
The genomic region encompassing the nephropathic cystinosis gene (CTNS): complete sequencing of a 200-kb segment and discovery of a novel gene within the common cystinosis-causing deletionJ W Touchman, Y Anikster, N L Dietrich, et al.
Nature Genetics|July 17, 2001
Mutation of a new gene causes a unique form of Hermansky-Pudlak syndrome in a genetic isolate of central Puerto RicoY Anikster, M Huizing, J White, et al.
Science (New York, N.Y.)|June 20, 1998
Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3A Wang, Y Liang, R A Fridell, et al.
Science (New York, N.Y.)|June 20, 1998
Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgeneF J Probst, R A Fridell, Y Raphael, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Genome Research|February 19, 1999
An effective approach for analyzing "prefinished" genomic sequence dataP M Kuehl, J M Weisemann, J W Touchman, et al.
Blood|February 9, 2000
Analysis of expressed immunoglobulin heavy chain genes in familial B-CLLA Sakai, G E Marti, N Caporaso, et al.
Journal of Virology|December 1, 1995
Branchpoint and polypyrimidine tract mutations mediating the loss and partial recovery of the Moloney murine sarcoma virus MuSVts110 thermosensitive splicing phenotypeJ W Touchman, I D'Souza, C A Heckman, et al.
Molecular Genetics and Metabolism|March 9, 1999
Identification and detection of the common 65-kb deletion breakpoint in the nephropathic cystinosis gene (CTNS)Y Anikster, C Lucero, J W Touchman, et al.
Genome Research|January 13, 2001
Human and mouse alpha-synuclein genes: comparative genomic sequence analysis and identification of a novel gene regulatory elementJ W Touchman, A Dehejia, O Chiba-Falek, et al.
Genome Research|March 1, 1997
2006 expressed-sequence tags derived from human chromosome 7-enriched cDNA librariesJ W Touchman, G G Bouffard, L A Weintraub, et al.
Genome Research|February 15, 2000
The genomic region encompassing the nephropathic cystinosis gene (CTNS): complete sequencing of a 200-kb segment and discovery of a novel gene within the common cystinosis-causing deletionJ W Touchman, Y Anikster, N L Dietrich, et al.
Nature Genetics|July 17, 2001
Mutation of a new gene causes a unique form of Hermansky-Pudlak syndrome in a genetic isolate of central Puerto RicoY Anikster, M Huizing, J White, et al.
Science (New York, N.Y.)|June 20, 1998
Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3A Wang, Y Liang, R A Fridell, et al.
Science (New York, N.Y.)|June 20, 1998
Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgeneF J Probst, R A Fridell, Y Raphael, et al.
Pageof 2