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Research 541–570 of 1000+
- Differential distribution and genetic determination of eccrine sweat glands and hair follicles in the volar skin of C57BL/6 mice and SD rats
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Examination of epigenetic inhibitor zebularine in treatment of skin wounds in healthy and diabetic mice
- Gender-Difference in Hair Length as Revealed by Crispr-Based Production of Long-Haired Mice with Dysfunctional FGF5 Mutations
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Assessment of hair and cashmere properties and their genetic background of several goat breeds in Southwest China
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- Mechanical forces across compartments coordinate cell shape and fate transitions to generate tissue architecture
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Human hair production by scalp samples grafted onto nude mice. Biochemical data on normal human hair and the genetic defect trichothiodystrophy
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Current Genetics in Hair Diseases
- Efficacy and safety of oral finasteride <i>versus</i> dutasteride in moderate-to-severe androgenetic alopecia in males based on trichoscopic and laboratory findings: a clinical comparison in Iran
- Revolutionary Approaches to Hair Regrowth: Follicle Neogenesis, Wnt/ß-Catenin Signaling, and Emerging Therapies
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Chemotherapy-Induced Alopecia by Docetaxel: Prevalence, Treatment and Prevention
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- C‐reactive protein as a novel biomarker for vitamin D deficiency in alopecia areata
- Ehlers-Danlos syndrome: From bedside to bench
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- ERG induces androgen receptor-mediated regulation of SOX9 in prostate cancer
- Independent genomewide screens identify the tumor suppressor VTRNA2-1 as a human epiallele responsive to periconceptional environment
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Comparative Spatial Transcriptomic and Single-Cell Analyses of Human Nail Units and Hair Follicles Show Transcriptional Similarities between the Onychodermis and Follicular Dermal Papilla
- Overexpression of hepatoma-derived growth factor in melanocytes does not lead to oncogenic transformation
- The RAIG Family Member, GPRC5D, Is Associated with Hard-Keratinized Structures