Sort   by:  
 Page size 
UnknownWhole genome sequencing reveals novel IGHMBP2 variant leading to unique cryptic splice-site and Charcot-Marie-Tooth phenotype with early onset symptoms.
Not available
S-EPMC6565564 | biostudies-literature
GenomicsWTCCC2 Ankylosing spondylitis cases - individual
WTCCC1 project Ankylosing Spondylitis (AS) samples
EGAD00000000010 | EGA
GenomicsWTCCC case-control study for Ankylosing Spondylitis - Combined Controls
WTCCC genome-wide case-control association study for Ankylosing Spondylitis (AS) - Combined Controls.
EGAS00000000019 | EGA
GenomicsWTCCC case-control study for Ankylosing Spondylitis
WTCCC genome-wide case-control association study for Ankylosing Spondylitis (AS) using the 1958 British Birth Cohort collection as controls.
EGAS00000000018 | EGA
UnknownGenome-wide Analyses Identify KIF5A as a Novel ALS Gene.
Not available
S-EPMC5867896 | biostudies-literature
UnknownHCK induces macrophage activation to promote renal inflammation and fibrosis via suppression of autophagy.
Not available
S-EPMC10354075 | biostudies-literature
UnknownModeling The Economic And Health Impact Of Increasing Children's Physical Activity In The United States.
Not available
S-EPMC5563819 | biostudies-literature
UnknownTumor Evolution and Drug Response in Patient-Derived Organoid Models of Bladder Cancer.
Not available
S-EPMC5890941 | biostudies-literature
UnknownHNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder.
Not available
S-EPMC10432175 | biostudies-literature
UnknownDe novo missense variants in ZBTB47 are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities.
Not available
S-EPMC11221546 | biostudies-literature
Sort   by:  
 Page size