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Research 421–450 of 830
- UDP-GlcNAc-1-Phosphotransferase Is a Clinically Important Regulator of Human and Mouse Hair Pigmentation
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor gene
- Effects of SLC45A2 and GPNMB on Melanin Deposition Based on Transcriptome Sequencing in Chicken Feather Follicles
- Analysis of Genome DNA Methylation at Inherited Coat Color Dilutions of Rex Rabbits
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Importance of Citrullination on Hair Protein Molecular Assembly During Trichocytic Differentiation
- Cutaneous Lymphadenoma Is a Distinct Trichoblastoma-like Lymphoepithelial Tumor With Diffuse Androgen Receptor Immunoreactivity, Notch1 Ligand in Reed-Sternberg–like Cells, and Common EGFR Somatic Mutations
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage
- Analogs of human genetic skin disease in domesticated animals
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Steatocystoma Multiplex
- Case report: Heterozygous mutation in HTRA1 causing typical cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
- Clinical and Genetic Aspects of Alopecia Areata: A Cutting Edge Review
- Exploring Hirsutism: Epidemiology, Associated Endocrinal Abnormalities, and Societal Challenges in GCC—A Narrative Review
- Human Regulatory T Cells: Understanding the Role of Tregs in Select Autoimmune Skin Diseases and Post-Transplant Nonmelanoma Skin Cancers
- Evolution of long scalp hair in humans
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Collodion baby to bathing suit ichthyosis: A 6-year follow-up
- Polymorphism of Keratin Gene KRT71 and Its Relationship with Wool Properties in Gansu Alpine Fine-Wool Sheep
- Integration Analysis of Transcriptome Sequencing and Whole-Genome Resequencing Reveal Wool Quality-Associated Key Genes in Zhexi Angora Rabbits
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Deciphering the molecular drivers for cashmere/pashmina fiber production in goats: a comprehensive review
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- Correlation Analysis of CXCL10, FOS, HOXC13, and WNT4 Gene Polymorphisms with Key Economic Traits—Initial Population Screening for Jiangnan Cashmere Goats
- Delayed hair cycle in mnd2 mutant mice lacking HtrA2 serine protease activity
- The feasibility and utility of hair follicle sampling to measure FMRP and FMR1 mRNA in children with or without fragile X syndrome: a pilot study
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome