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Blood
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May 6, 2009
Genetic variation in caspase genes and risk of non-Hodgkin lymphoma: a pooled analysis of 3 population-based case-control studies
Qing Lan, Lindsay M Morton, Bruce Armstrong, et al.
Human Molecular Genetics
|
October 17, 2017
Rare germline variants in known melanoma susceptibility genes in familial melanoma
Alisa M Goldstein, Yanzi Xiao, Joshua Sampson, et al.
European Journal of Haematology
|
January 23, 2015
Genetic susceptibility to diffuse large B-cell lymphoma in a pooled study of three Eastern Asian populations
Bryan A Bassig, James R Cerhan, Wing-Yan Au, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology
|
May 28, 2005
Association of multiple DRD2 polymorphisms with anorexia nervosa
Andrew W Bergen, Meredith Yeager, Robert A Welch, et al.
Plos One
|
April 25, 2009
Common gene variants in the tumor necrosis factor (TNF) and TNF receptor superfamilies and NF-kB transcription factors and non-Hodgkin lymphoma risk
Sophia S Wang, Mark P Purdue, James R Cerhan, et al.
Plos One
|
July 30, 2011
Comprehensive analysis of 5-aminolevulinic acid dehydrogenase (ALAD) variants and renal cell carcinoma risk among individuals exposed to lead
Dana M van Bemmel, Paolo Boffetta, Linda M Liao, et al.
Medrxiv : the Preprint Server for Health Sciences
|
September 4, 2023
Insights into the Mechanisms and Structure of Breakage-Fusion-Bridge Cycles in Cervical Cancer using Long-Read Sequencing
Isabel Rodriguez, Nicole M Rossi, Ayse Keskus, et al.
Papillomavirus Research (Amsterdam, Netherlands)
|
December 9, 2015
Deep sequencing of HPV16 genomes: A new high-throughput tool for exploring the carcinogenicity and natural history of HPV16 infection
Michael Cullen, Joseph F Boland, Mark Schiffman, et al.
Cancer Research
|
October 8, 2009
Apolipoprotein E/C1 locus variants modify renal cell carcinoma risk
Lee E Moore, Paul Brennan, Sara Karami, et al.
Plos Genetics
|
September 7, 2013
A recessive founder mutation in regulator of telomere elongation helicase 1, RTEL1, underlies severe immunodeficiency and features of Hoyeraal Hreidarsson syndrome
Bari J Ballew, Vijai Joseph, Saurav De, et al.
Page
of 40
Search research articles
Search
Showing results (231-240 of 398) with videos related to
Sort By:
Page
of 40
Blood
|
May 6, 2009
Genetic variation in caspase genes and risk of non-Hodgkin lymphoma: a pooled analysis of 3 population-based case-control studies
Qing Lan, Lindsay M Morton, Bruce Armstrong, et al.
Human Molecular Genetics
|
October 17, 2017
Rare germline variants in known melanoma susceptibility genes in familial melanoma
Alisa M Goldstein, Yanzi Xiao, Joshua Sampson, et al.
European Journal of Haematology
|
January 23, 2015
Genetic susceptibility to diffuse large B-cell lymphoma in a pooled study of three Eastern Asian populations
Bryan A Bassig, James R Cerhan, Wing-Yan Au, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology
|
May 28, 2005
Association of multiple DRD2 polymorphisms with anorexia nervosa
Andrew W Bergen, Meredith Yeager, Robert A Welch, et al.
Plos One
|
April 25, 2009
Common gene variants in the tumor necrosis factor (TNF) and TNF receptor superfamilies and NF-kB transcription factors and non-Hodgkin lymphoma risk
Sophia S Wang, Mark P Purdue, James R Cerhan, et al.
Plos One
|
July 30, 2011
Comprehensive analysis of 5-aminolevulinic acid dehydrogenase (ALAD) variants and renal cell carcinoma risk among individuals exposed to lead
Dana M van Bemmel, Paolo Boffetta, Linda M Liao, et al.
Medrxiv : the Preprint Server for Health Sciences
|
September 4, 2023
Insights into the Mechanisms and Structure of Breakage-Fusion-Bridge Cycles in Cervical Cancer using Long-Read Sequencing
Isabel Rodriguez, Nicole M Rossi, Ayse Keskus, et al.
Papillomavirus Research (Amsterdam, Netherlands)
|
December 9, 2015
Deep sequencing of HPV16 genomes: A new high-throughput tool for exploring the carcinogenicity and natural history of HPV16 infection
Michael Cullen, Joseph F Boland, Mark Schiffman, et al.
Cancer Research
|
October 8, 2009
Apolipoprotein E/C1 locus variants modify renal cell carcinoma risk
Lee E Moore, Paul Brennan, Sara Karami, et al.
Plos Genetics
|
September 7, 2013
A recessive founder mutation in regulator of telomere elongation helicase 1, RTEL1, underlies severe immunodeficiency and features of Hoyeraal Hreidarsson syndrome
Bari J Ballew, Vijai Joseph, Saurav De, et al.
Page
of 40