Search
for
Sort by
Research 481–510 of 1000+
- 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
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- The Cutaneous Epidermal Growth Factor Network: Can it be Translated Clinically to Stimulate Hair Growth?
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Concise Review: Human Dermis as an Autologous Source of Stem Cells for Tissue Engineering and Regenerative Medicine
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- The Notch Intracellular Domain Has an RBPj-Independent Role during Mouse Hair Follicular Development
- Essential Role for Integrin-Linked Kinase in Melanoblast Colonization of the Skin
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- The importance of basonuclin 2 in adult mice and its relation to basonuclin 1
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- The Study of Growth Factors in Patients with Androgenic Alopecia
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Nutritional Disorders of the Hair and Their Management
- GRowing an Epidermal Tumor
- Molecular Mechanisms of Hair Follicle Development
- Stem Cells in Regenerative Medicine: A Journey from Adult Stem Cells to Induced Pluripotent Cells
- A girl with loose anagen hair syndrome and concurrent uncombable hair syndrome
- AIRE Deficiency Leads to the Development of Alopecia Areata‒Like Lesions in Mice
- Diseases of Hair
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Hypoparathyroidism as the single major component for decades of autoimmune polyglandular syndrome type 1
- Combination of Transcriptomics and Proteomics Reveals Differentially Expressed Genes and Proteins in the Skin of EDAR Gene-Targeted and Wildtype Cashmere Goats
- Whole blood transcriptome profiling identifies candidate genes associated with alopecia in male giant pandas (Ailuropoda melanoleuca)
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Diseases of Hair
- A Case of Loose Anagen Hair Syndrome in a Southeast Asian Boy
- Retinoic Acid-Induced Epidermal Transdifferentiation in Skin