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Research 61–90 of 1000+
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Androgens and androgen receptor action in skin and hair follicles
- HRT for women with premature ovarian insufficiency: a comprehensive review
- Characterization of minoxidil/hydroxypropyl-β-cyclodextrin inclusion complex in aqueous alginate gel useful for alopecia management: Efficacy evaluation in male rat
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Tooth Development Associated with Mutations in Hereditary Vitamin D–Resistant Rickets
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- Characterization of novel TMEM173 mutation with additive IFIH1 risk allele
- Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development
- What causes hidradenitis suppurativa ?—15 years after
- Redefining hormone resistance in prostate cancer
- Molecular Genetics of Alopecias
- Pathogenesis and clinical features of alopecia in epidermolysis bullosa: A systematic review
- Presence of a Deletion Mutation (c.716delA) in the Ligand Binding Domain of the Vitamin D Receptor in an Indian Patient with Vitamin D-Dependent Rickets Type II
- Gender-Difference in Hair Length as Revealed by Crispr-Based Production of Long-Haired Mice with Dysfunctional FGF5 Mutations
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- The Genetics of Human Skin Disease
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Congenital hair loss disorders: Rare, but not too rare
- Molecular genetics of androgen insensitivity
- Two females with hair loss
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- Prevalence of CYP21 mutations and IRS1 variant among women with polycystic ovary syndrome and adrenal androgen excess
- Scd1 ab-Xyk : a new asebia allele characterized by a CCC trinucleotide insertion in exon 5 of the stearoyl-CoA desaturase 1 gene in mouse