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Research 331–360 of 1000+
- Characterization of Primary Cilia and Intraflagellar Transport 20 in the Epidermis
- British Society for Dermatopathology: Summaries of Papers
- Use of chemotherapy during human pregnancy
- Skin melanocytes: biology and development
- Wnt signaling: the good and the bad
- New clinico‐genetic classification of trichothiodystrophy
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Therapeutic effects of minoxidil high extra combination therapy in patients with androgenetic alopecia.
- [Genetic counseling in a case of neuro-ectodermosis: Vera Price trichothiodystrophy. Brittle hair with reduced sulfur content].
- [Treatment of androgenic alopecia with minoxidil].
- Involvement of Wnt, Eda and Shh at defined stages of sweat gland development
- 190 A cross-sectional study evaluating skin, hair, nail and bone disease in patients with focal dermal hypoplasia
- [Translated article] Keys to the Diagnosis of Hair Shaft Disorders: Part II
- Adult bone-marrow-derived mesenchymal stem cells contribute to wound healing of skin appendages
- Involvement of the Edar Signaling in the Control of Hair Follicle Involution (Catagen)
- p53‐dependent transcriptional regulation of EDA2R and its involvement in chemotherapy‐induced hair loss
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Type I Keratin 17 Protein Is Phosphorylated on Serine 44 by p90 Ribosomal Protein S6 Kinase 1 (RSK1) in a Growth- and Stress-dependent Fashion
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- A clinico-epidemiological study of scalp hair loss in children (0–18 years) in Kota Region, South-East Rajasthan
- [The Netherton syndrome with alopecia and prolinuria].
- Congenital atrichia associated with nevus flammeus: A rare association
- Coordinating the Sculptors: Ectodysplasin-A (EDA) Signaling Cross-Talk with Skeletogenic Pathways
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Uncombable hair improved by biotin
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Genetics of Alopecia
- Molecular Genetics of Human Hair Diseases