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Research 811–840 of 1000+
- Genetic Prediction of Eye, Hair, and Skin Color: Forensic Applications and Challenges in Latin American Populations
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- ‘Hard’ and ‘soft’ principles defining the structure, function and regulation of keratin intermediate filaments
- Genetic Basis of Male Pattern Baldness
- Keratin gene mutations in disorders of human skin and its appendages
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Hair follicle-specific keratins and their diseases
- Dlx3 is a crucial regulator of hair follicle differentiation and cycling
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Uncombable hair syndrome: Observations on response to biotin and occurrence in siblings with ectodermal dysplasia
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Hair: Its structure and response to cosmetic preparations
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Bone morphogenetic protein-2 (BMP-2) transactivates Dlx3 through Smad1 and Smad4: alternative mode for Dlx3 induction in mouse keratinocytes
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Trichoscopy in genetic hair shaft abnormalities
- Folliculin, the Product of the Birt-Hogg-Dube Tumor Suppressor Gene, Interacts with the Adherens Junction Protein p0071 to Regulate Cell-Cell Adhesion
- Aberrant Activation of the Hedgehog Signaling Pathway in Malignant Hematological Neoplasms
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Therapeutic Use of Botulinum Neurotoxins in Dermatology: Systematic Review
- Swiss Practice Recommendations for the Management of Hidradenitis Suppurativa/Acne Inversa
- Identification and characterization of Birt–Hogg–Dubé associated renal carcinoma
- The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects
- Dynamic expression of the zinc-finger transcription factor Trps1 during hair follicle morphogenesis and cycling
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Myotonic Dystrophy—A Progeroid Disease?
- Novel de novo pathogenic variant in the <i>ODC1</i> gene in a girl with developmental delay, alopecia, and dysmorphic features
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- A kindred with mutant IKAROS and autoimmunity