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Research 601–630 of 1000+
- The G60S Connexin43 Mutant Regulates Hair Growth and Hair Fiber Morphology in a Mouse Model of Human Oculodentodigital Dysplasia
- <i>Mrp4</i>, A New Mitogen-Regulated Protein/Proliferin Gene; Unique in this Gene Family for its Expression in the Adult Mouse Tail and Ear<sup>1</sup>
- Human epithelial stem cell survival within their niche requires “tonic” cannabinoid receptor 1‐signalling—Lessons from the hair follicle
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Global gene expression and comparison between multiple populations in the mouse epidermis
- Biotin and Acetazolamide for Treatment of an Unusual Child With Autism Plus Lack of Nail and Hair Growth
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- Novel D323G mutation of <i>DSG4</i> gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- [Peptidergic innervation in the sinus hair follicles of several mammalian species].
- Functional Analysis of VDR Gene Mutation R343H in A Child with Vitamin D-Resistant Rickets with Alopecia
- Porokeratotic eccrine and hair follicle nevus: a report of two cases and review of the literature
- Polymorphism in the A2M gene associated with high-quality milk in Murrah buffaloes (Bubalus bubalis)
- Telogen elongation in the hair cycle of <i>ob/ob</i> mice
- Identification of a recurrent nonsense mutation in <i>HR</i> gene responsible for atrichia with papular lesions in two Kashmiri families
- Effects of Guasha on histomorphology of scraped skins and on expression of calcitonin gene-related peptide and substance P in rats
- Deimination in epidermal barrier and hair formation
- Polycystic ovary syndrome is linked with the fat mass obesity (FTO) gene variants rs17817449 and rs1421085 in western Saudi Arabia
- Epilepsy and Neurodegeneration: Clues in the Hair and Blood Vessels!
- Human hair production by scalp samples grafted onto nude mice. Biochemical data on normal human hair and the genetic defect trichothiodystrophy
- Heterozygous deletion of the <i>NSDHL</i> gene in an Appenzeller Mountain Dog with verrucous epidermal keratinocytic nevi
- A Case to Tear One's Hair Out: Trichotillomania in Wilson's Disease
- Effect of Topical Grape Sap on Apoptosis in Hair Follicle Among Male Rats
- Why Do Not All Chemotherapy Patients Lose Their Hair? Answering an Intriguing Question
- A Newborn With Hair Loss
- Nevoid basal carcinoma syndrome (Gorlin syndrome) and pronounced androgenic alopecia in a woman with a novel mutation p.Leu1159fsx32 in the PTCH gene
- Epigenetic modifications may explain the relative protection of occipital hair follicles from androgenetic alopecia in men
- GCN5-mediated H3K27cr regulates hair follicle stem cell migration and hair follicle development through KRT80 activation
- Attenuated PER3 amplitude in hair follicles is associated with sleep irregularity in schizophrenia
- Case Report: A case of Rothmund–Thomson syndrome-like phenotype with an ANAPC1 variant of uncertain significance and observed hair improvement