Results 151 to 160 of about 1,875 (199)

Three novel heterozygous ANK1 loss-of-function variants cause hereditary spherocytosis in Chinese families. [PDF]

open access: yesAnn Hematol
Wang Y   +8 more
europepmc   +1 more source

ANK3 as a Novel Genetic Biomarker for Liafensine in Treatment-Resistant Depression: The ENLIGHTEN Randomized Clinical Trial. [PDF]

open access: yesJAMA Psychiatry
Wang G   +14 more
europepmc   +1 more source

CXCL9 and CXCL10 Induce Expression of Nociceptive Ion Channels in Primary Sensory Neurons in Models of HIV-Associated Distal Sensory Polyneuropathy. [PDF]

open access: yesInt J Mol Sci
Warfield R   +9 more
europepmc   +1 more source

Metabolic-Epigenetic Crosstalk in Takayasu Arteritis: The ANK2-MAVS-IL-8 Axis as a Novel Therapeutic Paradigm. [PDF]

open access: yesInt J Mol Sci
Xie T   +11 more
europepmc   +1 more source

Impaired AIS plasticity in ankyrin-G mutant mice alters cortical excitability and behavior. [PDF]

open access: yesProc Natl Acad Sci U S A
Li M   +11 more
europepmc   +1 more source

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