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Research 481–510 of 1000+
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Retinoic Acid and Mouse Skin Morphogenesis. II. Role of Epidermal Competence in Hair Glandular Metaplasia
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- Is there association between thyroid stimulating hormone levels and the four phenotypes in polycystic ovary syndrome?
- Soluble CD83 improves and accelerates wound healing by the induction of pro-resolving macrophages
- The possible implication of the S250C variant of the autoimmune regulator protein in a patient with autoimmunity and immunodeficiency: in silico analysis suggests a molecular pathogenic mechanism for the variant
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Identification of novel mutation in the<i>HR</i>gene responsible for atrichia with papular lesions in a Pakistani family
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- Reviewer #2 (Public Review): CaBP1 and 2 enable sustained CaV1.3 calcium currents and synaptic transmission in inner hair cells
- Author response: Type XVII collagen coordinates proliferation in the interfollicular epidermis
- Decision letter: Type XVII collagen coordinates proliferation in the interfollicular epidermis
- Analyse de la régulation du gène Hairless et identification des voies de signalisation affectées chez les mutants «bald Mill Hill».
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- CCDC22 and CCDC93, two potential retriever-interacting proteins, are required for root and root hair growth in Arabidopsis
- Collodion baby to bathing suit ichthyosis: A 6-year follow-up
- ATP-competitive mTOR kinase inhibitors delay plant growth by triggering early differentiation of meristematic cells but no developmental patterning change
- `Cyclic alopecia' in<i>Msx2</i>mutants: defects in hair cycling and hair shaft differentiation
- Inflammatory priming enhances mesenchymal stromal cell secretome potential as a clinical product for regenerative medicine approaches through secreted factors and EV-miRNAs: the example of joint disease
- Spontaneous Squamous Cell Carcinoma Induced by the Somatic Inactivation of <i>Retinoblastoma</i> and <i>Trp53</i> Tumor Suppressors
- Expression of <i>Foxi3</i> is regulated by ectodysplasin in skin appendage placodes
- Atrichia with papular lesions resulting from mutations in the rhesus macaque (<i>Macaca mulatta</i>) <i>hairless</i> gene
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Increased 25(OH)D3 level in redheaded people: Could redheadedness be an adaptation to temperate climate?
- 1329 CENPV is a novel CYLD-interacting molecule regulating ciliary acetylated tubulin
- Insertional mutation of the hairless locus on mouse Chromosome 14
- Association between <i>EGF</i> and <i>EGFR</i> Gene Polymorphisms and Susceptibility to Alopecia Areata in the Korean Population
- Characterization of the Role of Transferrin receptor 1 (Tfr1) in the Intestinal Epithelium, Pancreas, and Skin