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Research 421–450 of 1000+
- Review of Stem Cell Therapy for Hair Loss
- Signaling pathways and targeted therapeutic strategies for polycystic ovary syndrome
- A patient with Cronkhite-Canada syndrome whose entire digestive tracts was examined endoscopically
- Gonads
- The in vitro plasticity of hair follicle dermal and mesenchymal stem cells
- Hair Today
- Oral Retinoids in Dermatology
- Fibroblast heterogeneity and tertiary lymphoid tissues in the kidney
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- 190 A cross-sectional study evaluating skin, hair, nail and bone disease in patients with focal dermal hypoplasia
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Coordinating the Sculptors: Ectodysplasin-A (EDA) Signaling Cross-Talk with Skeletogenic Pathways
- Bone morphogenetic protein-2 (BMP-2) transactivates Dlx3 through Smad1 and Smad4: alternative mode for Dlx3 induction in mouse keratinocytes
- Sostdc1 defines the size and number of skin appendage placodes
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- A Case Report of Cronkhite-Canada Syndrome Complicated by Membranous Nephropathy
- Transcriptomic landscape of early hair follicle and epidermal development
- Cases Report the Cronkhite-Canada Syndrome
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Runx3 is involved in hair shape determination
- ASH2L mediates epidermal differentiation and hair follicle morphogenesis via H3K4me3 modification
- An Unusual Case of Diarrhea, Dysgeusia, and Grainy and Nodular Mucosa
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Wnt Signaling Across Adult Skin Mini-Organs: Interfollicular Epidermis, Hair Follicle, and Nail—Implications for Disease and Regeneration
- Successful topical minoxidil treatment for hair density and length in trichorhinophalangeal syndrome type 1
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors