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Genome Research
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January 17, 2003
Pericentromeric duplications in the laboratory mouse
James W Thomas, Mary G Schueler, Tyrone J Summers, et al.
American Journal of Human Genetics
|
December 31, 2005
Mutations in TRIOBP, which encodes a putative cytoskeletal-organizing protein, are associated with nonsyndromic recessive deafness
Saima Riazuddin, Shaheen N Khan, Zubair M Ahmed, et al.
Genome Research
|
January 10, 2002
Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome
Udaya DeSilva, Laura Elnitski, Jacquelyn R Idol, et al.
BMC Genomics
|
March 18, 2014
Identification of candidate genes involved in coronary artery calcification by transcriptome sequencing of cell lines
Shurjo K Sen, Jennifer J Barb, Praveen F Cherukuri, et al.
Nature Genetics
|
August 28, 2014
Data use under the NIH GWAS data sharing policy and future directions
Dina N Paltoo, Laura Lyman Rodriguez, Michael Feolo, et al.
Cell
|
July 22, 2025
Human-specific gene expansions contribute to brain evolution
Daniela C Soto, José M Uribe-Salazar, Gulhan Kaya, et al.
Biorxiv : the Preprint Server for Biology
|
October 10, 2024
Gene expansions contributing to human brain evolution
Daniela C Soto, José M Uribe-Salazar, Gulhan Kaya, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 6, 2012
Specific inactivation of two immunomodulatory SIGLEC genes during human evolution
Xiaoxia Wang, Nivedita Mitra, Ismael Secundino, et al.
Genomics
|
August 6, 2002
Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins
Razia Sultana, Chang-En Yu, Jun Yu, et al.
BMC Genomics
|
July 18, 2009
The value of avian genomics to the conservation of wildlife
Michael N Romanov, Elaina M Tuttle, Marlys L Houck, et al.
Page
of 18
Search research articles
Search
Showing results (131-140 of 175) with videos related to
Sort By:
Page
of 18
Genome Research
|
January 17, 2003
Pericentromeric duplications in the laboratory mouse
James W Thomas, Mary G Schueler, Tyrone J Summers, et al.
American Journal of Human Genetics
|
December 31, 2005
Mutations in TRIOBP, which encodes a putative cytoskeletal-organizing protein, are associated with nonsyndromic recessive deafness
Saima Riazuddin, Shaheen N Khan, Zubair M Ahmed, et al.
Genome Research
|
January 10, 2002
Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome
Udaya DeSilva, Laura Elnitski, Jacquelyn R Idol, et al.
BMC Genomics
|
March 18, 2014
Identification of candidate genes involved in coronary artery calcification by transcriptome sequencing of cell lines
Shurjo K Sen, Jennifer J Barb, Praveen F Cherukuri, et al.
Nature Genetics
|
August 28, 2014
Data use under the NIH GWAS data sharing policy and future directions
Dina N Paltoo, Laura Lyman Rodriguez, Michael Feolo, et al.
Cell
|
July 22, 2025
Human-specific gene expansions contribute to brain evolution
Daniela C Soto, José M Uribe-Salazar, Gulhan Kaya, et al.
Biorxiv : the Preprint Server for Biology
|
October 10, 2024
Gene expansions contributing to human brain evolution
Daniela C Soto, José M Uribe-Salazar, Gulhan Kaya, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 6, 2012
Specific inactivation of two immunomodulatory SIGLEC genes during human evolution
Xiaoxia Wang, Nivedita Mitra, Ismael Secundino, et al.
Genomics
|
August 6, 2002
Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins
Razia Sultana, Chang-En Yu, Jun Yu, et al.
BMC Genomics
|
July 18, 2009
The value of avian genomics to the conservation of wildlife
Michael N Romanov, Elaina M Tuttle, Marlys L Houck, et al.
Page
of 18