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C Murray

Showing results (1241-1250 of 1,465) with videos related to

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Plos One|August 13, 2013
A mutation in mouse Pak1ip1 causes orofacial clefting while human PAK1IP1 maps to 6p24 translocation breaking points associated with orofacial cleftingAdam P Ross, M Adela Mansilla, Youngshik Choe, et al.
Journal of Medical Genetics|April 14, 2012
Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphaloceleUppala Radhakrishna, Swapan K Nath, Ken McElreavey, et al.
Cell|October 20, 2018
Targeting Processive Transcription Elongation via SEC Disruption for MYC-Induced Cancer TherapyKaiwei Liang, Edwin R Smith, Yuki Aoi, et al.
Genetic Epidemiology|December 3, 2016
Whole exome association of rare deletions in multiplex oral cleft familiesJack Fu, Terri H Beaty, Alan F Scott, et al.
RMD Open|November 1, 2023
Improved lung cancer clinical outcomes in patients with autoimmune rheumatic diseasesPaola Ghanem, Joseph C Murray, Kristen A Marrone, et al.
Journal of the American College of Nutrition|November 3, 2010
The effect of increasing consumption of pulses and wholegrains in obese people: a randomized controlled trialBernard J Venn, Tracy Perry, Tim J Green, et al.
Plos One|April 25, 2013
X-chromosomal maternal and fetal SNPs and the risk of spontaneous preterm delivery in a Danish/Norwegian genome-wide association studySolveig Myking, Heather A Boyd, Ronny Myhre, et al.
American Journal of Human Genetics|December 27, 2011
Exome sequence identifies RIPK4 as the Bartsocas-Papas syndrome locusKaren Mitchell, James O'Sullivan, Caterina Missero, et al.
HGG Advances|April 5, 2021
The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lipSarah W Curtis, Daniel Chang, Myoung Keun Lee, et al.
American Journal of Medical Genetics. Part A|January 21, 2016
Evaluation of proton-coupled folate transporter (SLC46A1) polymorphisms as risk factors for neural tube defects and oral cleftsJulia E VanderMeer, Tonia C Carter, Faith Pangilinan, et al.
Pageof 147

Showing results (1241-1250 of 1,465) with videos related to

Sort By:
Pageof 147
Plos One|August 13, 2013
A mutation in mouse Pak1ip1 causes orofacial clefting while human PAK1IP1 maps to 6p24 translocation breaking points associated with orofacial cleftingAdam P Ross, M Adela Mansilla, Youngshik Choe, et al.
Journal of Medical Genetics|April 14, 2012
Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphaloceleUppala Radhakrishna, Swapan K Nath, Ken McElreavey, et al.
Cell|October 20, 2018
Targeting Processive Transcription Elongation via SEC Disruption for MYC-Induced Cancer TherapyKaiwei Liang, Edwin R Smith, Yuki Aoi, et al.
Genetic Epidemiology|December 3, 2016
Whole exome association of rare deletions in multiplex oral cleft familiesJack Fu, Terri H Beaty, Alan F Scott, et al.
RMD Open|November 1, 2023
Improved lung cancer clinical outcomes in patients with autoimmune rheumatic diseasesPaola Ghanem, Joseph C Murray, Kristen A Marrone, et al.
Journal of the American College of Nutrition|November 3, 2010
The effect of increasing consumption of pulses and wholegrains in obese people: a randomized controlled trialBernard J Venn, Tracy Perry, Tim J Green, et al.
Plos One|April 25, 2013
X-chromosomal maternal and fetal SNPs and the risk of spontaneous preterm delivery in a Danish/Norwegian genome-wide association studySolveig Myking, Heather A Boyd, Ronny Myhre, et al.
American Journal of Human Genetics|December 27, 2011
Exome sequence identifies RIPK4 as the Bartsocas-Papas syndrome locusKaren Mitchell, James O'Sullivan, Caterina Missero, et al.
HGG Advances|April 5, 2021
The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lipSarah W Curtis, Daniel Chang, Myoung Keun Lee, et al.
American Journal of Medical Genetics. Part A|January 21, 2016
Evaluation of proton-coupled folate transporter (SLC46A1) polymorphisms as risk factors for neural tube defects and oral cleftsJulia E VanderMeer, Tonia C Carter, Faith Pangilinan, et al.
Pageof 147