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Research 631–660 of 1000+
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Frizzled Receptors in Development and Disease
- Folliculin, the Product of the Birt-Hogg-Dube Tumor Suppressor Gene, Interacts with the Adherens Junction Protein p0071 to Regulate Cell-Cell Adhesion
- Nevus comedonicus syndrome: a case associated with multiple basal cell carcinomas and a rudimentary toe
- The Story of the Finest Armor: Developmental Aspects of Reptile Skin
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Molecular characterization of caprine<i>KRTAP13-3</i>in Liaoning cashmere goat in China
- Hair casts
- Constitutive activation of Stat3 in mouse epidermis is linked to hair deficiency and cytoskeletal network damage
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- Localized Epidermolysis Bullosa Simplex (Weber-Cockayne type)
- Morgellon's syndrome. Evidence of a microorganism causing an unexplained dermopathy
- A genetic electrophoretic variant of high-sulfur hair proteins for forensic hair comparisons. I. Characterization of variant high-sulfur proteins of human hair.
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Genetic hair and nail disorders
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Biochemical Evidence That Small Proline-rich Proteins and Trichohyalin Function in Epithelia by Modulation of the Biomechanical Properties of Their Cornified Cell Envelopes
- Beta-caryophyllene enhances wound healing through multiple routes
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- Analyses of histological and transcriptome differences in the skin of short-hair and long-hair rabbits
- A Scarless Healing Tale: Comparing Homeostasis and Wound Healing of Oral Mucosa With Skin and Oesophagus
- Acquired Progressive Kinking of the Hair
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Abstracts
- Transcriptome analysis reveals the genetic basis underlying the formation and seasonal changes of nuptial pads in Rana chensinensis
- The Roles of Keratinocytes in the Initiation, Progression and Maintenance of Hidradenitis Suppurativa
- Linear and Unilateral Basaloid Follicular Hamartoma Along Blaschko’s Lines in an Elderly Patient: A Rare Presentation
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2