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Research 301–330 of 1000+
- A frameshift mutation in the TRPS1 gene showing a mild phenotype of trichorhinophalangeal syndrome type 1
- Androgenetic alopecia
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Towards Defining the Pathogenesis of the Hairless Phenotype
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- Stimuli-responsive nanoformulations for CRISPR-Cas9 genome editing
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- WRKY transcription factors (TFs): Molecular switches to regulate drought, temperature, and salinity stresses in plants
- A kindred with mutant IKAROS and autoimmunity
- BLIMP1 Is Required for Postnatal Epidermal Homeostasis but Does Not Define a Sebaceous Gland Progenitor under Steady-State Conditions
- DNA Damage-Inducible Transcript 4 Is an Innate Surveillant of Hair Follicular Stress in Vitamin D Receptor Knockout Mice and a Regulator of Wound Re-Epithelialization
- Protein S-Palmitoylation as Potential Therapeutic Target for Dermatoses
- The role of vitamin D receptor mutations in the development of alopecia
- Targeting of Smoothened for therapeutic gain
- Role of the Autoimmune Regulator (<i>AIRE</i>) gene in alopecia areata: Strong association of a potentially functional <i>AIRE</i> polymorphism with alopecia universalis
- Newly Developed Targeted Therapies Against the Androgen Receptor in Triple-Negative Breast Cancer: A Review
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets
- Androgens/Androgen Receptor in the Management of Skin Diseases
- The role of vitamin D receptor signaling in hair follicle health and alopecia: Current understanding and therapeutic implications
- CXXC5 Mediates DHT-Induced Androgenetic Alopecia via PGD2
- Dermal Blimp1 Acts Downstream of Epidermal TGFβ and Wnt/β-Catenin to Regulate Hair Follicle Formation and Growth
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- The Autoimmune Regulator (AIRE), Which Is Defective in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Patients, Is Expressed in Human Epidermal and Follicular Keratinocytes and Associates With the Intermediate Filament Protein Cytokeratin 17
- Krox20 in epithelial and glial stem cells and their niches
- How to defeat male pattern alopecia in a trompeur de femmes, who loves to abuse of libido boosters?
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans