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Research 241–270 of 1000+
- Comparison of Androgenetic Alopecia Prevalence in Paternal and Maternal Male Family Members of Male Androgenetic Alopecia Patients
- The β‐thymosins: Intracellular and extracellular activities of a versatile actin binding protein family
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- The sheep KAP8-2 gene, a new KAP8 family member that is absent in humans
- Efficacy and safety of the oral Janus kinase 3/tyrosine kinase expressed in hepatocellular carcinoma family kinase inhibitor ritlecitinib over 24 months: integrated analysis of the ALLEGRO phase IIb/III and long-term phase III clinical studies in alopecia areata
- COPD at the end of life: Predictors of the emotional distress of patients and their family caregivers
- Impact of Pediatric Alopecia Areata on Quality of Life of Patients and Their Family Members: A Nationwide Multicenter Questionnaire Study
- The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach
- Subcellular localization of the five members of the human steroid 5α-reductase family
- Characterization of the Human Hair Shaft Cuticle–Specific Keratin-Associated Protein 10 Family
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor gene
- The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- A novel point mutation of keratin 17 (<i>KRT17</i>) in a Japanese family with pachyonychia congenita type 2: an RNA-based genetic analysis using a single hair bulb
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- An alternative diagnostic method of eruptive vellus hair cysts: Report of a familial case with pruritus
- In vivo Assessment of the Antinociceptive Activity of Ethanol Bark Extract of Thevetia peruviana (Family: Apocynaceae) in Swiss Albino Mice
- [Analysis of human hair basic keratin 6 gene mutation in a Chinese Han family with monilethrix].
- Description of clinical aspects and microscopy of the hair shaft of a carrier of familial monilethrix
- The fatty acids and the skin: a focus on the n-6 family of unsaturated fatty acids
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- Comparative evaluation of potential phytopharmacological and nutritional properties of some Indigenous rhizomes of Zingiberaceae family (Alpinia calcarata, Alpinia galanga, Alpinia zerumbet) localized in Southeast Asia
- THE UNMET NEEDS OF LUPUS PATIENTS: CREATING VISIBILITY AND SUPPORTING PATIENTS AND FAMILIES IN THEIR JOURNEY
- A cross-sectional study for alopecia patterns, family history, and diet, reveals early-onset hair loss in residents of Saudi Arabia and a lack of awareness about available treatments
- Hair steroid before and after COVID-19 in preschoolers: the moderation of family characteristics
- Autosomal dominant monilethrix with incomplete penetrance due to a novel KRT86 mutation in a Chinese family
- The fatty acids and the skin: a focus on the n-6 family of unsaturated fatty acids
- Polycystic Ovaries Are Inherited as an Autosomal Dominant Trait: Analysis of 29 Polycystic Ovary Syndrome and 10 Control Families