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Nucleic Acids Research
|
November 19, 2015
WormBase 2016: expanding to enable helminth genomic research
Kevin L Howe, Bruce J Bolt, Scott Cain, et al.
Plos Genetics
|
November 7, 2023
Dominant negative variants in KIF5B cause osteogenesis imperfecta via down regulation of mTOR signaling
Ronit Marom, Bo Zhang, Megan E Washington, et al.
Genetics
|
February 8, 2022
WormBase in 2022-data, processes, and tools for analyzing Caenorhabditis elegans
Paul Davis, Magdalena Zarowiecki, Valerio Arnaboldi, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 17, 2025
Dominant negative ATP5F1A variants disrupt oxidative phosphorylation causing neurological disorders
Sara M Fielder, Marisa W Friederich, Daniella H Hock, et al.
EMBO Molecular Medicine
|
August 26, 2025
Dominant negative ATP5F1A variants disrupt oxidative phosphorylation causing neurological disorders
Sara M Fielder, Marisa W Friederich, Daniella H Hock, et al.
Human Molecular Genetics
|
August 8, 2023
Macrocephaly and developmental delay caused by missense variants in RAB5C
Klaas Koop, Weimin Yuan, Federico Tessadori, et al.
American Journal of Human Genetics
|
January 29, 2025
Sequence variants in HECTD1 result in a variable neurodevelopmental disorder
Gazelle Zerafati-Jahromi, Elias Oxman, Hieu D Hoang, et al.
Nature Communications
|
September 10, 2024
Variants in LRRC7 lead to intellectual disability, autism, aggression and abnormal eating behaviors
Jana Willim, Daniel Woike, Daniel Greene, et al.
Science (New York, N.Y.)
|
October 31, 2024
Brain malformations and seizures by impaired chaperonin function of TRiC
Florian Kraft, Piere Rodriguez-Aliaga, Weimin Yuan, et al.
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Search research articles
Search
Showing results (81-90 of 89) with videos related to
Sort By:
Page
of 9
You have reached the last page of results.
This site can display upto 89 results.
Nucleic Acids Research
|
November 19, 2015
WormBase 2016: expanding to enable helminth genomic research
Kevin L Howe, Bruce J Bolt, Scott Cain, et al.
Plos Genetics
|
November 7, 2023
Dominant negative variants in KIF5B cause osteogenesis imperfecta via down regulation of mTOR signaling
Ronit Marom, Bo Zhang, Megan E Washington, et al.
Genetics
|
February 8, 2022
WormBase in 2022-data, processes, and tools for analyzing Caenorhabditis elegans
Paul Davis, Magdalena Zarowiecki, Valerio Arnaboldi, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 17, 2025
Dominant negative ATP5F1A variants disrupt oxidative phosphorylation causing neurological disorders
Sara M Fielder, Marisa W Friederich, Daniella H Hock, et al.
EMBO Molecular Medicine
|
August 26, 2025
Dominant negative ATP5F1A variants disrupt oxidative phosphorylation causing neurological disorders
Sara M Fielder, Marisa W Friederich, Daniella H Hock, et al.
Human Molecular Genetics
|
August 8, 2023
Macrocephaly and developmental delay caused by missense variants in RAB5C
Klaas Koop, Weimin Yuan, Federico Tessadori, et al.
American Journal of Human Genetics
|
January 29, 2025
Sequence variants in HECTD1 result in a variable neurodevelopmental disorder
Gazelle Zerafati-Jahromi, Elias Oxman, Hieu D Hoang, et al.
Nature Communications
|
September 10, 2024
Variants in LRRC7 lead to intellectual disability, autism, aggression and abnormal eating behaviors
Jana Willim, Daniel Woike, Daniel Greene, et al.
Science (New York, N.Y.)
|
October 31, 2024
Brain malformations and seizures by impaired chaperonin function of TRiC
Florian Kraft, Piere Rodriguez-Aliaga, Weimin Yuan, et al.
Page
of 9