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Research 511–540 of 1000+
- Dermatological drugs, topical agents, and cosmetics
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Gene Expression During Drosophila Wing Morphogenesis and Differentiation
- Alopecia in Epidermolysis Bullosa
- Le gène<i>hairless</i>de la souris
- The Skin and Subcutaneous Tissues
- Hair Loss: A Harbinger of the Morbidities to Come!
- 316 Specialized ribosomes in human dermal fibroblast senescence
- Marie-unna hereditary hypotrichosis
- Urticaria, Drug Hypersensitivity Rashes, Nodules and Tumors, and Atrophic Diseases
- Low Level Laser and Light Therapy
- Hair and scalp disorders
- Zinc transporter ZIP13 G289R variant from Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS) is associated with abnormal hair quality
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Three-dimensional architecture and linearized mapping of vibrissa follicle afferents
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- LITERATURE REVIEW
- Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene
- Novel Mutation in the Hemojuvelin Gene (HJV) in a Patient with Juvenile Hemochromatosis Presenting with Insulin-dependent Diabetes Mellitus, Secondary Hypothyroidism and Hypogonadism
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome
- Melanocyte stem cells: a melanocyte reservoir in hair follicles for hair and skin pigmentation
- Safety assessment of cyclin-dependent kinase 4/6 inhibitors and comparison of time to adverse events
- Androgenetic Alopecia: Therapy Update
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- Male infertility and genitourinary birth defects: there is more than meets the eye
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Stress-sensing in the human greying hair follicle: Ataxia Telangiectasia Mutated (ATM) depletion in hair bulb melanocytes in canities-prone scalp
- Hair Follicle-Related MicroRNA-34a Serum Expression and rs2666433A/G Variant in Patients with Alopecia: A Cross-Sectional Analysis