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UnknownThe Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains.
Not available
S-EPMC24264 | biostudies-literature
UnknownParental age effects and Rett syndrome.
Not available
S-EPMC11911005 | biostudies-literature
UnknownPhenotypic features in MECP2 duplication syndrome: Effects of age.
Not available
S-EPMC8000774 | biostudies-literature
UnknownMolecular and functional characterization of Kv 7 channels in penile arteries and corpus cavernosum of healthy and metabolic syndrome rats.
Not available
S-EPMC4831315 | biostudies-literature
UnknownAnalysis of X-inactivation status in a Rett syndrome natural history study cohort.
Not available
S-EPMC9034674 | biostudies-literature
UnknownThe array of clinical phenotypes of males with mutations in Methyl-CpG binding protein 2.
Not available
S-EPMC6488031 | biostudies-literature
UnknownTMEM16A is implicated in the regulation of coronary flow and is altered in hypertension.
Not available
S-EPMC6514379 | biostudies-literature
UnknownCharacterizing the phenotypic effect of Xq28 duplication size in MECP2 duplication syndrome.
Not available
S-EPMC6465105 | biostudies-literature
UnknownCrucial role for sensory nerves and Na/H exchanger inhibition in dapagliflozin- and empagliflozin-induced arterial relaxation.
Not available
S-EPMC11587556 | biostudies-literature
UnknownBuilding Bridges in a Series of Estrogen Receptor Degraders: An Application of Metathesis in Medicinal Chemistry.
Not available
S-EPMC6792171 | biostudies-literature
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