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Mathew T Pletcher

Showing results (31-40 of 37) with videos related to

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Nature Reviews. Drug Discovery|May 18, 2021
Clinical trial strategies for rare neurodevelopmental disorders: challenges and opportunitiesMichelle L Krishnan, Elizabeth Berry-Kravis, Jamie K Capal, et al.
Nature Genetics|February 16, 2005
Uncovering regulatory pathways that affect hematopoietic stem cell function using 'genetical genomics'Leonid Bystrykh, Ellen Weersing, Bert Dontje, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 4, 2003
Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouseTim Wiltshire, Mathew T Pletcher, Serge Batalov, et al.
Elife|April 13, 2013
Usf1, a suppressor of the circadian Clock mutant, reveals the nature of the DNA-binding of the CLOCK:BMAL1 complex in miceKazuhiro Shimomura, Vivek Kumar, Nobuya Koike, et al.
Visual Neuroscience|April 14, 2007
Generation, identification and functional characterization of the nob4 mutation of Grm6 in the mouseLawrence H Pinto, Martha H Vitaterna, Kazuhiro Shimomura, et al.
Investigative Ophthalmology & Visual Science|March 28, 2015
Identification of a Novel Mucin Gene HCG22 Associated With Steroid-Induced Ocular HypertensionShinwu Jeong, Nitin Patel, Christopher K Edlund, et al.
Nature Neuroscience|March 7, 2017
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorderRyan K C Yuen, Daniele Merico, Matt Bookman, et al.
Pageof 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Nature Reviews. Drug Discovery|May 18, 2021
Clinical trial strategies for rare neurodevelopmental disorders: challenges and opportunitiesMichelle L Krishnan, Elizabeth Berry-Kravis, Jamie K Capal, et al.
Nature Genetics|February 16, 2005
Uncovering regulatory pathways that affect hematopoietic stem cell function using 'genetical genomics'Leonid Bystrykh, Ellen Weersing, Bert Dontje, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 4, 2003
Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouseTim Wiltshire, Mathew T Pletcher, Serge Batalov, et al.
Elife|April 13, 2013
Usf1, a suppressor of the circadian Clock mutant, reveals the nature of the DNA-binding of the CLOCK:BMAL1 complex in miceKazuhiro Shimomura, Vivek Kumar, Nobuya Koike, et al.
Visual Neuroscience|April 14, 2007
Generation, identification and functional characterization of the nob4 mutation of Grm6 in the mouseLawrence H Pinto, Martha H Vitaterna, Kazuhiro Shimomura, et al.
Investigative Ophthalmology & Visual Science|March 28, 2015
Identification of a Novel Mucin Gene HCG22 Associated With Steroid-Induced Ocular HypertensionShinwu Jeong, Nitin Patel, Christopher K Edlund, et al.
Nature Neuroscience|March 7, 2017
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorderRyan K C Yuen, Daniele Merico, Matt Bookman, et al.
Pageof 4