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Anatomically and Functionally Distinct Lung Mesenchymal Populations Marked by Lgr5 and Lgr6.
Not available
S-EPMC5607351
|
biostudies-literature
Cite
New Kidney Allocation System Associated With Increased Rates Of Transplants Among Black And Hispanic Patients.
Not available
S-EPMC5681858
|
biostudies-literature
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The BRAIN Initiative Cell Census Consortium: Lessons Learned toward Generating a Comprehensive Brain Cell Atlas.
Not available
S-EPMC5689454
|
biostudies-literature
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Recurrent dominant mutations affecting two adjacent residues in the motor domain of the monomeric kinesin KIF22 result in skeletal dysplasia and joint laxity.
Not available
S-EPMC3234368
|
biostudies-literature
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m<sup>6</sup>A/YTHDF2-mediated mRNA decay targets TGF-β signaling to suppress the quiescence acquisition of early postnatal mouse hippocampal NSCs.
Not available
S-EPMC11698649
|
biostudies-literature
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CRTAP and LEPRE1 mutations in recessive osteogenesis imperfecta.
Not available
S-EPMC2671575
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biostudies-literature
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C9orf72 deficiency promotes microglial-mediated synaptic loss in aging and amyloid accumulation.
Not available
S-EPMC8298293
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biostudies-literature
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Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes.
Not available
S-EPMC9470534
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biostudies-literature
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Proteome-wide association study and functional validation identify novel protein markers for pancreatic ductal adenocarcinoma.
Not available
S-EPMC11010651
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biostudies-literature
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Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome.
Not available
S-EPMC1180579
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biostudies-literature
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