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Mark Lathrop

Showing results (61-70 of 443) with videos related to

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European Journal of Human Genetics : EJHG|January 31, 2008
The exon 1-8C/G SNP in the PSMA6 gene contributes only a small amount to the burden of myocardial infarction in 6946 cases and 2720 controls from a United Kingdom populationDerrick A Bennett, Peng Xu, Robert Clarke, et al.
BMC Genomics|May 29, 2009
Genetic analysis of an F(2) intercross between two chicken lines divergently selected for body-weightPer Wahlberg, Orjan Carlborg, Mario Foglio, et al.
The European Respiratory Journal|July 18, 2020
The undiagnosed disease burden associated with alpha-1 antitrypsin deficiency genotypesTomoko Nakanishi, Vincenzo Forgetta, Tomohiro Handa, et al.
JCO Precision Oncology|August 1, 2024
Germline Susceptibility to Renal Cell Carcinoma and Implications for Genetic ScreeningKate I Glennon, Mikiko Endo, Yoshiaki Usui, et al.
The American Journal of Clinical Nutrition|July 10, 2015
Neuropeptide Y genotype, central obesity, and abdominal fat distribution: the POUNDS LOST trialXiaochen Lin, Qibin Qi, Yan Zheng, et al.
Blood|August 23, 2007
The HBS1L-MYB intergenic region on chromosome 6q23.3 influences erythrocyte, platelet, and monocyte counts in humansStephan Menzel, Jie Jiang, Nicholas Silver, et al.
Annals of Hematology|September 1, 2005
Genomewide linkage analysis of soluble transferrin receptor plasma levelsAngel F Remacha, Joan C Souto, José Manuel Soria, et al.
European Journal of Human Genetics : EJHG|April 26, 2002
DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34Mirna Mustapha, Eliane Chouery, Sébastien Chardenoux, et al.
Human Genetics|December 17, 2002
A novel locus for autosomal dominant nonsyndromic hearing loss (DFNA44) maps to chromosome 3q28-29Silvia Modamio-Høybjør, Miguel Angel Moreno-Pelayo, Angeles Mencía, et al.
Journal of Human Genetics|July 8, 2011
A polymorphism of the POLG2 gene is genetically associated with the invasiveness of urinary bladder cancer in Japanese malesChanavee Ratanajaraya, Hiroyuki Nishiyama, Meiko Takahashi, et al.
Pageof 45

Showing results (61-70 of 443) with videos related to

Sort By:
Pageof 45
European Journal of Human Genetics : EJHG|January 31, 2008
The exon 1-8C/G SNP in the PSMA6 gene contributes only a small amount to the burden of myocardial infarction in 6946 cases and 2720 controls from a United Kingdom populationDerrick A Bennett, Peng Xu, Robert Clarke, et al.
BMC Genomics|May 29, 2009
Genetic analysis of an F(2) intercross between two chicken lines divergently selected for body-weightPer Wahlberg, Orjan Carlborg, Mario Foglio, et al.
The European Respiratory Journal|July 18, 2020
The undiagnosed disease burden associated with alpha-1 antitrypsin deficiency genotypesTomoko Nakanishi, Vincenzo Forgetta, Tomohiro Handa, et al.
JCO Precision Oncology|August 1, 2024
Germline Susceptibility to Renal Cell Carcinoma and Implications for Genetic ScreeningKate I Glennon, Mikiko Endo, Yoshiaki Usui, et al.
The American Journal of Clinical Nutrition|July 10, 2015
Neuropeptide Y genotype, central obesity, and abdominal fat distribution: the POUNDS LOST trialXiaochen Lin, Qibin Qi, Yan Zheng, et al.
Blood|August 23, 2007
The HBS1L-MYB intergenic region on chromosome 6q23.3 influences erythrocyte, platelet, and monocyte counts in humansStephan Menzel, Jie Jiang, Nicholas Silver, et al.
Annals of Hematology|September 1, 2005
Genomewide linkage analysis of soluble transferrin receptor plasma levelsAngel F Remacha, Joan C Souto, José Manuel Soria, et al.
European Journal of Human Genetics : EJHG|April 26, 2002
DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34Mirna Mustapha, Eliane Chouery, Sébastien Chardenoux, et al.
Human Genetics|December 17, 2002
A novel locus for autosomal dominant nonsyndromic hearing loss (DFNA44) maps to chromosome 3q28-29Silvia Modamio-Høybjør, Miguel Angel Moreno-Pelayo, Angeles Mencía, et al.
Journal of Human Genetics|July 8, 2011
A polymorphism of the POLG2 gene is genetically associated with the invasiveness of urinary bladder cancer in Japanese malesChanavee Ratanajaraya, Hiroyuki Nishiyama, Meiko Takahashi, et al.
Pageof 45