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Science (New York, N.Y.)
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February 12, 2005
Comparison of fine-scale recombination rates in humans and chimpanzees
Wendy Winckler, Simon R Myers, Daniel J Richter, et al.
Nature Genetics
|
February 10, 2006
Common deletion polymorphisms in the human genome
Steven A McCarroll, Tracy N Hadnott, George H Perry, et al.
Population Health Management
|
February 3, 2023
Clinical and Cost Benefits of Anti-Obesity Medication for US Veterans Participating in the MOVE! Weight Management Program
W Timothy Garvey, Mu Cheng, Abhilasha Ramasamy, et al.
Frontiers in Cell and Developmental Biology
|
February 28, 2025
CFAP410 has a bimodular architecture with a conserved surface patch on its N-terminal leucine-rich repeat motif for binding interaction partners
Alexander Stadler, Heloisa B Gabriel, Laryssa V De Liz, et al.
Molecular Psychiatry
|
July 26, 2002
Family-based association study of 76 candidate genes in bipolar disorder: BDNF is a potential risk locus. Brain-derived neutrophic factor
P Sklar, S B Gabriel, M G McInnis, et al.
Nature Genetics
|
April 16, 2002
Segregation at three loci explains familial and population risk in Hirschsprung disease
Stacey B Gabriel, Rémi Salomon, Anna Pelet, et al.
Plos Genetics
|
April 19, 2012
Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism
Maria H Chahrour, Timothy W Yu, Elaine T Lim, et al.
Cancer Discovery
|
May 16, 2012
High-throughput detection of actionable genomic alterations in clinical tumor samples by targeted, massively parallel sequencing
Nikhil Wagle, Michael F Berger, Matthew J Davis, et al.
Malaria Journal
|
June 6, 2013
Cloning and characterization of bifunctional enzyme farnesyl diphosphate/geranylgeranyl diphosphate synthase from Plasmodium falciparum
Fabiana M Jordão, Heloisa B Gabriel, João M P Alves, et al.
Human Molecular Genetics
|
January 8, 2011
Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13
Minal Çalışkan, Jessica X Chong, Lawrence Uricchio, et al.
Page
of 35
Search research articles
Search
Showing results (201-210 of 347) with videos related to
Sort By:
Page
of 35
Science (New York, N.Y.)
|
February 12, 2005
Comparison of fine-scale recombination rates in humans and chimpanzees
Wendy Winckler, Simon R Myers, Daniel J Richter, et al.
Nature Genetics
|
February 10, 2006
Common deletion polymorphisms in the human genome
Steven A McCarroll, Tracy N Hadnott, George H Perry, et al.
Population Health Management
|
February 3, 2023
Clinical and Cost Benefits of Anti-Obesity Medication for US Veterans Participating in the MOVE! Weight Management Program
W Timothy Garvey, Mu Cheng, Abhilasha Ramasamy, et al.
Frontiers in Cell and Developmental Biology
|
February 28, 2025
CFAP410 has a bimodular architecture with a conserved surface patch on its N-terminal leucine-rich repeat motif for binding interaction partners
Alexander Stadler, Heloisa B Gabriel, Laryssa V De Liz, et al.
Molecular Psychiatry
|
July 26, 2002
Family-based association study of 76 candidate genes in bipolar disorder: BDNF is a potential risk locus. Brain-derived neutrophic factor
P Sklar, S B Gabriel, M G McInnis, et al.
Nature Genetics
|
April 16, 2002
Segregation at three loci explains familial and population risk in Hirschsprung disease
Stacey B Gabriel, Rémi Salomon, Anna Pelet, et al.
Plos Genetics
|
April 19, 2012
Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism
Maria H Chahrour, Timothy W Yu, Elaine T Lim, et al.
Cancer Discovery
|
May 16, 2012
High-throughput detection of actionable genomic alterations in clinical tumor samples by targeted, massively parallel sequencing
Nikhil Wagle, Michael F Berger, Matthew J Davis, et al.
Malaria Journal
|
June 6, 2013
Cloning and characterization of bifunctional enzyme farnesyl diphosphate/geranylgeranyl diphosphate synthase from Plasmodium falciparum
Fabiana M Jordão, Heloisa B Gabriel, João M P Alves, et al.
Human Molecular Genetics
|
January 8, 2011
Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13
Minal Çalışkan, Jessica X Chong, Lawrence Uricchio, et al.
Page
of 35