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Research 61–90 of 80
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Developmentally regulated expression of integrin alpha-6 distinguishes neural crest derivatives in the skin
- Neurotoxins Acting at Synaptic Sites: A Brief Review on Mechanisms and Clinical Applications
- Caffeine Induces Autophagy and Apoptosis in Auditory Hair Cells via the SGK1/HIF-1α Pathway
- Immunohistochemical, pharmacovigilance, and omics analyses reveal the involvement of ATP-sensitive K+ channel subunits in cancers: role in drug–disease interactions
- Special collection on inward rectifying K<sup>+</sup> channels
- Endocrine abnormalities in ring chromosome 11: a case report and review of the literature
- Dynamic Transcriptome Profile Analysis of Mechanisms Related to Melanin Deposition in Chicken Muscle Development
- Mechanical stimulation of human hair follicle outer root sheath cultures activates adjacent sensory neurons
- Multiple cell types guided by neurocytes orchestrate horn bud initiation in dairy goats
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Investigation of Transcriptional Gene Profiling in Normal Murine Hair Follicular Substructures Using Next-Generation Sequencing to Provide Potential Insights into Skin Disease
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Histopathological change of age-related hearing loss in female advance-aged CBA/CaJ mice
- Molecular heterogeneity of quiescent melanocyte stem cells revealed by single‐cell RNA‐sequencing
- E-Poster
- Examining the Effect of Notocactus ottonis Cold Vacuum Isolated Plant Cell Extract on Hair Growth in C57BL/6 Mice Using a Combination of Physiological and OMICS Analyses
- Comprehensive transcriptome data to identify downstream genes of testosterone signalling in dermal papilla cells
- Bridging Personal and Population in Excitability Diseases: Will Studies of Rare Diseases Bring Generalizable Mechanisms From Monogenic Channelopathies?
- https://researchopenworld.com/genetics-of-hidradenitis-suppurativa/#
- KCNQ4 K+ channels tune mechanoreceptors for normal touch sensation in mouse and man
- KCNQ Potassium Channels Modulate Sensitivity of Skin Down-hair (D-hair) Mechanoreceptors
- Auditory Threshold Variability in the SAMP8 Mouse Model of Age-Related Hearing Loss: Functional Loss and Phenotypic Change Precede Outer Hair Cell Loss
- Genetic basis of polycystic ovary syndrome
- Genetics of Polycystic Ovary Syndrome
- The Possible Involvement of KATP Channels in Cholestatic Pruritus in Mice
- Effects of steroid hormones on the expression of Ca2+ activated K+ channels in in vitro pituitary cells of Atlantic cod (Gadus morhua)
- Author response: The signaling lipid sphingosine 1-phosphate regulates mechanical pain
- Exome analysis for Cronkhite-Canada syndrome: A case report
- Decision letter: The signaling lipid sphingosine 1-phosphate regulates mechanical pain