Search
for
Sort by
Research 601–630 of 693
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Keratins and disease at a glance
- Prevention and management of dermatological toxicities related to anticancer agents: ESMO Clinical Practice Guidelines☆
- RASopathic Skin Eruptions during Vemurafenib Therapy
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- The molecular basis of human keratin disorders
- The Two Functional Keratin 6 Genes of Mouse Are Differentially Regulated and Evolved Independently from Their Human Orthologs
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- A new mutation Rim3 resembling Re den is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11
- Keratins and skin disease
- New clinico‐genetic classification of trichothiodystrophy
- Alteration of Skin Properties with Autologous Dermal Fibroblasts
- Genetics of Inherited Ichthyoses and Related Diseases
- Cylindroma as Tumor of Hair Follicle Origin
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Dynamic expression of Runx1 in skin affects hair structure
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- A Scarless Healing Tale: Comparing Homeostasis and Wound Healing of Oral Mucosa With Skin and Oesophagus
- Complete Structure of an Epithelial Keratin Dimer: Implications for Intermediate Filament Assembly
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Reconstitution of full-thickness skin by microcolumn grafting
- Ichthyosis with confetti: clinics, molecular genetics and management
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Comedonal and Cystic Fibrofolliculomas in Birt-Hogg-Dube Syndrome
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Photobiomodulation therapy in management of cancer therapy-induced side effects: WALT position paper 2022