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N Udar

Showing results (11-20 of 20) with videos related to

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American Journal of Human Genetics|July 1, 1996
Ataxia-telangiectasia: mutations in ATM cDNA detected by protein-truncation screeningM Telatar, Z Wang, N Udar, et al.
Cornea|May 5, 2009
Hydrogen peroxide causes mitochondrial DNA damage in corneal epithelial cellsShari R Atilano, Marilyn Chwa, Dae W Kim, et al.
Genetic Testing|January 1, 1997
An allelic variant at the ATM locus is implicated in breast cancer susceptibilityG P Larson, G Zhang, S Ding, et al.
Genomics|June 15, 1997
A transcript map encompassing the multiple endocrine neoplasia type-1 (MEN1) locus on chromosome 11q13M Sawicki, E Arnold, S Ebrahimi, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 1, 1997
CAND3: a ubiquitously expressed gene immediately adjacent and in opposite transcriptional orientation to the ATM gene at 11q23.1X Chen, L Yang, N Udar, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 13, 2016
CAND3: A ubiquitously expressed gene immediately adjacent and in opposite transcriptional orientation to the ATM gene at 1lq23.1X Chen, L Yang, N Udar, et al.
Molecular Vision|January 5, 2000
North Carolina macular dystrophy (MCDR1) locus: a fine resolution genetic map and haplotype analysisK W Small, N Udar, S Yelchits, et al.
American Journal of Human Genetics|March 7, 1998
Ataxia-telangiectasia: identification and detection of founder-effect mutations in the ATM gene in ethnic populationsM Telatar, S Teraoka, Z Wang, et al.
International Journal of Radiation Biology|December 1, 1994
Genetic haplotyping of ataxia-telangiectasia families localizes the major gene to an approximately 850 kb region on chromosome 11q23.1R A Gatti, E Lange, G Rotman, et al.
Human Molecular Genetics|July 27, 2001
Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype--phenotype correlationE De Baere, M J Dixon, K W Small, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
American Journal of Human Genetics|July 1, 1996
Ataxia-telangiectasia: mutations in ATM cDNA detected by protein-truncation screeningM Telatar, Z Wang, N Udar, et al.
Cornea|May 5, 2009
Hydrogen peroxide causes mitochondrial DNA damage in corneal epithelial cellsShari R Atilano, Marilyn Chwa, Dae W Kim, et al.
Genetic Testing|January 1, 1997
An allelic variant at the ATM locus is implicated in breast cancer susceptibilityG P Larson, G Zhang, S Ding, et al.
Genomics|June 15, 1997
A transcript map encompassing the multiple endocrine neoplasia type-1 (MEN1) locus on chromosome 11q13M Sawicki, E Arnold, S Ebrahimi, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 1, 1997
CAND3: a ubiquitously expressed gene immediately adjacent and in opposite transcriptional orientation to the ATM gene at 11q23.1X Chen, L Yang, N Udar, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 13, 2016
CAND3: A ubiquitously expressed gene immediately adjacent and in opposite transcriptional orientation to the ATM gene at 1lq23.1X Chen, L Yang, N Udar, et al.
Molecular Vision|January 5, 2000
North Carolina macular dystrophy (MCDR1) locus: a fine resolution genetic map and haplotype analysisK W Small, N Udar, S Yelchits, et al.
American Journal of Human Genetics|March 7, 1998
Ataxia-telangiectasia: identification and detection of founder-effect mutations in the ATM gene in ethnic populationsM Telatar, S Teraoka, Z Wang, et al.
International Journal of Radiation Biology|December 1, 1994
Genetic haplotyping of ataxia-telangiectasia families localizes the major gene to an approximately 850 kb region on chromosome 11q23.1R A Gatti, E Lange, G Rotman, et al.
Human Molecular Genetics|July 27, 2001
Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype--phenotype correlationE De Baere, M J Dixon, K W Small, et al.
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