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Showing results (1051-1060 of 1,064) with videos related to
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Science (New York, N.Y.)
|
May 20, 2000
Galileo at Io: results from high-resolution imaging
A S McEwen, M J Belton, H H Breneman, et al.
Human Mutation
|
July 22, 2014
Mutation of POC1B in a severe syndromic retinal ciliopathy
Bodo B Beck, Jennifer B Phillips, Malte P Bartram, et al.
The Medical Journal of Australia
|
February 24, 2022
COVID-19 vaccination in children and adolescents aged 5 years and older undergoing treatment for cancer and non-malignant haematological conditions: Australian and New Zealand Children's Haematology/Oncology Group consensus statement
Eliska Furlong, Rishi S Kotecha, Rachel Conyers, et al.
Science Robotics
|
May 21, 2025
Autonomous surface sampling for the Europa Lander mission concept
J J Bowkett, S A Chien, Y Marchetti, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 11, 2021
Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11
Thomas A Ravenscroft, Jennifer B Phillips, Elizabeth Fieg, et al.
Genomics
|
July 20, 2005
A physical map of the genome of Atlantic salmon, Salmo salar
Siemon H S Ng, Carlo G Artieri, Ian E Bosdet, et al.
Ecology Letters
|
August 19, 2025
Pollinator-Promoting Interventions in European Urban Habitats-A Synthesis
Gabriella Süle, András Báldi, David Kleijn, et al.
Nature
|
May 24, 2023
A small-molecule PI3Kα activator for cardioprotection and neuroregeneration
Grace Q Gong, Benoit Bilanges, Ben Allsop, et al.
American Journal of Human Genetics
|
November 24, 2020
BICRA, a SWI/SNF Complex Member, Is Associated with BAF-Disorder Related Phenotypes in Humans and Model Organisms
Scott Barish, Tahsin Stefan Barakat, Brittany C Michel, et al.
American Journal of Human Genetics
|
October 6, 2018
A Recurrent De Novo Heterozygous COG4 Substitution Leads to Saul-Wilson Syndrome, Disrupted Vesicular Trafficking, and Altered Proteoglycan Glycosylation
Carlos R Ferreira, Zhi-Jie Xia, Aurélie Clément, et al.
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of 107
Search research articles
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Showing results (1051-1060 of 1,064) with videos related to
Sort By:
Page
of 107
Science (New York, N.Y.)
|
May 20, 2000
Galileo at Io: results from high-resolution imaging
A S McEwen, M J Belton, H H Breneman, et al.
Human Mutation
|
July 22, 2014
Mutation of POC1B in a severe syndromic retinal ciliopathy
Bodo B Beck, Jennifer B Phillips, Malte P Bartram, et al.
The Medical Journal of Australia
|
February 24, 2022
COVID-19 vaccination in children and adolescents aged 5 years and older undergoing treatment for cancer and non-malignant haematological conditions: Australian and New Zealand Children's Haematology/Oncology Group consensus statement
Eliska Furlong, Rishi S Kotecha, Rachel Conyers, et al.
Science Robotics
|
May 21, 2025
Autonomous surface sampling for the Europa Lander mission concept
J J Bowkett, S A Chien, Y Marchetti, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 11, 2021
Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11
Thomas A Ravenscroft, Jennifer B Phillips, Elizabeth Fieg, et al.
Genomics
|
July 20, 2005
A physical map of the genome of Atlantic salmon, Salmo salar
Siemon H S Ng, Carlo G Artieri, Ian E Bosdet, et al.
Ecology Letters
|
August 19, 2025
Pollinator-Promoting Interventions in European Urban Habitats-A Synthesis
Gabriella Süle, András Báldi, David Kleijn, et al.
Nature
|
May 24, 2023
A small-molecule PI3Kα activator for cardioprotection and neuroregeneration
Grace Q Gong, Benoit Bilanges, Ben Allsop, et al.
American Journal of Human Genetics
|
November 24, 2020
BICRA, a SWI/SNF Complex Member, Is Associated with BAF-Disorder Related Phenotypes in Humans and Model Organisms
Scott Barish, Tahsin Stefan Barakat, Brittany C Michel, et al.
American Journal of Human Genetics
|
October 6, 2018
A Recurrent De Novo Heterozygous COG4 Substitution Leads to Saul-Wilson Syndrome, Disrupted Vesicular Trafficking, and Altered Proteoglycan Glycosylation
Carlos R Ferreira, Zhi-Jie Xia, Aurélie Clément, et al.
Page
of 107