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Research 151–180 of 1000+
- Footprints of the EADV: a meeting report from the 17th Congress of the European Academy of Dermatology and Venereology
- Evaluation and treatment of male and female pattern hair loss
- Androgenetic alopecia in men
- Subject Index
- ALOPECIA AREATA-A CLINICAL ANALYSIS
- Transgenic mice display hair loss and regrowth overexpressing mutant <i>Hr</i> gene
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Expert consensus on the management of telogen effluvium in India
- Telogen Effluvium
- An analytical study of serum ferritin, vitamin D, and thyroid function in females with diffuse hair loss
- Trichoscopy as an essential diagnostic technique for hair and scalp disorders in skin of color: A case-control study
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Mutations in the Serum/Glucocorticoid Regulated Kinase 3 (Sgk3) Are Responsible for the Mouse Fuzzy (fz) Hair Phenotype
- Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis
- Multicentric calcified trichilemmal cysts with alopecia universalis affecting siblings
- Poly(rC) binding protein 2 acts as a negative regulator of IRES-mediated translation of Hr mRNA
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- 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>)
- Molecular Genetics of Human Hair Diseases
- Hypotrichosis in a child with olmsted syndrome
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Eyebrow Loss
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome