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Research 661–690 of 1000+
- Isolated autosomal recessive woolly hair/hypotrichosis: genetics, pathogenesis and therapies
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Loose anagen hair syndrome
- Congenital hypotrichosis - treatment with topical minoxidil and hair dye
- Renbök phenomenon: Alopecia areata sparing psoriasis plaques
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Trps1 activates a network of secreted Wnt inhibitors and transcription factors crucial to vibrissa follicle morphogenesis
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Identification of Ectodysplasin Target Genes Reveals the Involvement of Chemokines in Hair Development
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Premature termination of hair follicle morphogenesis and accelerated hair follicle cycling in Iasi congenital atrichia (fz<sup>ica</sup>) mice points to <i>fuzzy</i> as a key element of hair cycle control
- The G60S Connexin43 Mutant Regulates Hair Growth and Hair Fiber Morphology in a Mouse Model of Human Oculodentodigital Dysplasia
- Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells
- Roles of MED1 in Quiescence of Hair Follicle Stem Cells and Maintenance of Normal Hair Cycling
- Menkes Syndrome Presenting as Myoclonic Seizures: Neuroimaging and EEG Observations
- Cutaneous Complications of Artificial Hair Implantation: A Pathological Study
- STUDIES ON A SKIN CALCIFYING SYSTEM
- Practical Aspects of Hair Transplantation in Asians
- Mutations in the Serum/Glucocorticoid Regulated Kinase 3 (Sgk3) Are Responsible for the Mouse Fuzzy (fz) Hair Phenotype
- Pathological Studies of Cross‐Related Congenital Hypotrichosis in Cattle
- A discriminant multi-scale histopathology descriptor using dictionary learning
- A weighted non-negative matrix factorization approach to predict potential associations between drug and disease
- The Near-Naked Hairless (Hr) Mutation Disrupts Hair Formation but Is Not Due to a Mutation in the Hairless Coding Region
- Toward Elucidating Epigenetic and Metabolic Regulation of Stem Cell Lineage Plasticity in Skin Aging
- The overexpression of R-spondin 3 affects hair morphogenesis and hair development along with the formation and maturation of the hair follicle stem cells
- Congenital hypotrichosis in a French bulldog
- Coexistence of giant blue nevus of the scalp with hair loss and alopecia areata
- Congenital Hypotrichosis in a White-Tailed Deer Fawn from South Dakota
- Homozygous missense mutation in the<i>LIPH</i>gene causing autosomal recessive hypotrichosis simplex in a Chinese patient
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.