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Kate T Montgomery

Showing results (1-10 of 8) with videos related to

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Current Protocols in Human Genetics|October 31, 2008
PolyPhred analysis software for mutation detection from fluorescence-based sequence dataKate T Montgomery, Oleg Iartchouck, Li Li, et al.
Current Protocols in Human Genetics|April 23, 2008
Mutation detection using automated fluorescence-based sequencingKate T Montgomery, Oleg Iartchouck, Li Li, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|June 25, 2008
Evaluation of the Golgi trafficking protein VPS54 (wobbler) as a candidate for ALSMiriam H Meisler, Carsten Russ, Kate T Montgomery, et al.
Nature Genetics|December 5, 2006
Germline gain-of-function mutations in SOS1 cause Noonan syndromeAmy E Roberts, Toshiyuki Araki, Kenneth D Swanson, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 25, 2005
Genomic characterization of non-O1, non-O139 Vibrio cholerae reveals genes for a type III secretion systemMichelle Dziejman, Davide Serruto, Vincent C Tam, et al.
Blood|February 11, 2016
Clinical and laboratory variability in a cohort of patients diagnosed with type 1 VWD in the United StatesVeronica H Flood, Pamela A Christopherson, Joan Cox Gill, et al.
Nature|December 6, 2002
Initial sequencing and comparative analysis of the mouse genome, Robert H Waterston, Kerstin Lindblad-Toh, et al.
Nature|March 17, 2006
The finished DNA sequence of human chromosome 12Steven E Scherer, Donna M Muzny, Christian J Buhay, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Current Protocols in Human Genetics|October 31, 2008
PolyPhred analysis software for mutation detection from fluorescence-based sequence dataKate T Montgomery, Oleg Iartchouck, Li Li, et al.
Current Protocols in Human Genetics|April 23, 2008
Mutation detection using automated fluorescence-based sequencingKate T Montgomery, Oleg Iartchouck, Li Li, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|June 25, 2008
Evaluation of the Golgi trafficking protein VPS54 (wobbler) as a candidate for ALSMiriam H Meisler, Carsten Russ, Kate T Montgomery, et al.
Nature Genetics|December 5, 2006
Germline gain-of-function mutations in SOS1 cause Noonan syndromeAmy E Roberts, Toshiyuki Araki, Kenneth D Swanson, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 25, 2005
Genomic characterization of non-O1, non-O139 Vibrio cholerae reveals genes for a type III secretion systemMichelle Dziejman, Davide Serruto, Vincent C Tam, et al.
Blood|February 11, 2016
Clinical and laboratory variability in a cohort of patients diagnosed with type 1 VWD in the United StatesVeronica H Flood, Pamela A Christopherson, Joan Cox Gill, et al.
Nature|December 6, 2002
Initial sequencing and comparative analysis of the mouse genome, Robert H Waterston, Kerstin Lindblad-Toh, et al.
Nature|March 17, 2006
The finished DNA sequence of human chromosome 12Steven E Scherer, Donna M Muzny, Christian J Buhay, et al.
Pageof 1