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Research 121–150 of 133
- Decision letter: Sphingosine 1-phosphate-regulated transcriptomes in heterogenous arterial and lymphatic endothelium of the aorta
- Author response: The molecular basis for ANE syndrome revealed by the large ribosomal subunit processome interactome
- The structure and organization of lanceolate mechanosensory complexes at mouse hair follicles
- The role of WNT10B in physiology and disease: A 10-year update
- Genetically separable determinants of hair keratin gene expression
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- Two-ligand priming mechanism for potentiated phosphoinositide synthesis is an evolutionarily conserved feature of Sec14-like phosphatidylinositol and phosphatidylcholine exchange proteins
- Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants
- Sex-limited chromosomes and non-reproductive traits
- Transcriptional regulation of the thymus master regulator <i>Foxn1</i>
- From Diagnosis to Prognosis: A Scoping Review of Artificial Intelligence in Alopecia Research
- CPK1 activates CNGCs through phosphorylation for Ca2+ signaling to promote root hair growth in Arabidopsis
- eLife Assessment: The Drosophila hematopoietic niche assembles through collective cell migration controlled by neighbor tissues and Slit-Robo signaling
- Genotype-phenotype correlation in boys with X-linked hypohidrotic ectodermal dysplasia
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Identification of dkk4 as a target of Eda-A1/Edar pathway reveals an unexpected role of ectodysplasin as inhibitor of Wnt signalling in ectodermal placodes
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- The Genetics of Human Skin Disease
- Ectodysplasin Signaling in Cutaneous Appendage Development: Dose, Duration, and Diversity
- Laminin-511 is an epithelial message promoting dermal papilla development and function during early hair morphogenesis
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- Cutaneous Retinoic Acid Levels Determine Hair Follicle Development and Downgrowth
- Sostdc1 defines the size and number of skin appendage placodes
- Wnt10b Regulation of Hair Follicle Development, Regeneration, and Skin Diseases
- Mice humanised for the EGF receptor display hypomorphic phenotypes in skin, bone and heart
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Hypomorphic mutation in the hairless gene accelerates pruritic atopic skin caused by feeding a special diet to mice
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice