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Mutation Research
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February 15, 2005
Detection and frequency estimation of rare variants in pools of genomic DNA from large populations using mutational spectrometry
Xiao-Cheng Li-Sucholeiki, Aoy Tomita-Mitchell, Kevin Arnold, et al.
Human Genomics
|
December 17, 2004
Development of an integrated genome informatics, data management and workflow infrastructure: a toolbox for the study of complex disease genetics
Oliver S Burren, Barry C Healy, Alex C Lam, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
February 16, 2000
Phase I and pharmacokinetic study of farnesyl protein transferase inhibitor R115777 in advanced cancer
J Zujewski, I D Horak, C J Bol, et al.
Human Molecular Genetics
|
July 1, 1996
The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 diabetes. Belgian Diabetes Registry
L Nisticò, R Buzzetti, L E Pritchard, et al.
Diabetes
|
September 28, 2004
Analysis of the vitamin D receptor gene sequence variants in type 1 diabetes
Sergey Nejentsev, Jason D Cooper, Lisa Godfrey, et al.
Nature Genetics
|
October 18, 2005
Population structure, differential bias and genomic control in a large-scale, case-control association study
David G Clayton, Neil M Walker, Deborah J Smyth, et al.
Nature Genetics
|
October 5, 2001
Haplotype tagging for the identification of common disease genes
G C Johnson, L Esposito, B J Barratt, et al.
Nature Genetics
|
November 3, 2019
The impact of proinflammatory cytokines on the β-cell regulatory landscape provides insights into the genetics of type 1 diabetes
Mireia Ramos-Rodríguez, Helena Raurell-Vila, Maikel L Colli, et al.
Nature Genetics
|
November 5, 2021
Identification of LZTFL1 as a candidate effector gene at a COVID-19 risk locus
Damien J Downes, Amy R Cross, Peng Hua, et al.
Plos Genetics
|
January 28, 2006
Genetic analysis of completely sequenced disease-associated MHC haplotypes identifies shuffling of segments in recent human history
James A Traherne, Roger Horton, Anne N Roberts, et al.
Page
of 90
Search research articles
Search
Showing results (831-840 of 895) with videos related to
Sort By:
Page
of 90
Mutation Research
|
February 15, 2005
Detection and frequency estimation of rare variants in pools of genomic DNA from large populations using mutational spectrometry
Xiao-Cheng Li-Sucholeiki, Aoy Tomita-Mitchell, Kevin Arnold, et al.
Human Genomics
|
December 17, 2004
Development of an integrated genome informatics, data management and workflow infrastructure: a toolbox for the study of complex disease genetics
Oliver S Burren, Barry C Healy, Alex C Lam, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
February 16, 2000
Phase I and pharmacokinetic study of farnesyl protein transferase inhibitor R115777 in advanced cancer
J Zujewski, I D Horak, C J Bol, et al.
Human Molecular Genetics
|
July 1, 1996
The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 diabetes. Belgian Diabetes Registry
L Nisticò, R Buzzetti, L E Pritchard, et al.
Diabetes
|
September 28, 2004
Analysis of the vitamin D receptor gene sequence variants in type 1 diabetes
Sergey Nejentsev, Jason D Cooper, Lisa Godfrey, et al.
Nature Genetics
|
October 18, 2005
Population structure, differential bias and genomic control in a large-scale, case-control association study
David G Clayton, Neil M Walker, Deborah J Smyth, et al.
Nature Genetics
|
October 5, 2001
Haplotype tagging for the identification of common disease genes
G C Johnson, L Esposito, B J Barratt, et al.
Nature Genetics
|
November 3, 2019
The impact of proinflammatory cytokines on the β-cell regulatory landscape provides insights into the genetics of type 1 diabetes
Mireia Ramos-Rodríguez, Helena Raurell-Vila, Maikel L Colli, et al.
Nature Genetics
|
November 5, 2021
Identification of LZTFL1 as a candidate effector gene at a COVID-19 risk locus
Damien J Downes, Amy R Cross, Peng Hua, et al.
Plos Genetics
|
January 28, 2006
Genetic analysis of completely sequenced disease-associated MHC haplotypes identifies shuffling of segments in recent human history
James A Traherne, Roger Horton, Anne N Roberts, et al.
Page
of 90