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Research 811–840 of 1000+
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- Identification of two additional novel mutations in the AR gene associated with severe forms of androgen insensitivity syndrome
- Catecholaminergic neurons boost fibroblast osteogenic activity in keloid
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome
- Deciphering gene regulatory programs in mouse embryonic skin through single-cell multiomics analysis
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Recent advances in neuropeptide-related omics and gene editing: Spotlight on NPY and somatostatin and their roles in growth and food intake of fish
- Bridging Personal and Population in Excitability Diseases: Will Studies of Rare Diseases Bring Generalizable Mechanisms From Monogenic Channelopathies?
- Estudo da diversidade dos genes MC1R e SLC24A5 em populações globais: avaliação de aspectos evolutivos e ambientais
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- Analysis of LncRNA-mRNA Co-Expression Profiles in Patients With Polycystic Ovary Syndrome: A Pilot Study
- Single-cell transcriptomics reveals hair growth retardation mediated by aberrant connective tissue sheath contraction in male androgenetic alopecia
- An integrative analysis of the lncRNA-miRNA-mRNA competitive endogenous RNA network reveals potential mechanisms in the murine hair follicle cycle
- The use of mesenchymal stromal cells in the treatment of coronavirus disease 2019
- [Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
- Skin Microbiome Shifts in Various Dermatological Conditions
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Generalized multiple eruptive milia in an infant – An unusual presentation
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Mutation in 5′ upstream region of <i>GCH</i> I gene causes familial dopa-responsive dystonia
- Epigenetics of Colorectal Cancer
- WRKY transcription factors (TFs): Molecular switches to regulate drought, temperature, and salinity stresses in plants
- Expression of Hypothalamic–Pituitary–Thyroid Axis RelatedGenes in the Human Skin
- Biochemical Evidence That Small Proline-rich Proteins and Trichohyalin Function in Epithelia by Modulation of the Biomechanical Properties of Their Cornified Cell Envelopes
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development
- Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia