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Research 511–540 of 1000+
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Biology of Human Hair: Know Your Hair to Control It
- Induction of dermal fibroblasts into dermal papilla cell-like cells in hydrogel microcapsules for enhanced hair follicle regeneration
- Identification of differentially expressed genes in actinic keratosis samples treated with ingenol mebutate gel
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Androgen receptor gene polymorphism and biological age markers in men
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Causal associations between plasma proteins and prostate cancer: a Proteome-Wide Mendelian Randomization
- Nevus Sebaceus With Novel HRAS Sequence Variant Mutation Misdiagnosed as Alopecia Areata
- Integrative Whole-Transcriptome Sequencing Analysis of Skin Tissues with Different Coat Types in Cashmere Goats Across Stages of Hair Follicle Development
- Multiple cell types guided by neurocytes orchestrate horn bud initiation in dairy goats
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Siberian cats help in solving part of the mystery surrounding golden cats
- Several variants on chromosome 10 are associated with coarse hair diameter in Dazu black goats (<i>Capra hircus</i>)
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- A replication study confirmed the EDAR gene to be a major contributor to population differentiation regarding head hair thickness in Asia
- Chronic overlapping pain conditions and nociplastic pain
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Transcriptome Profiling and Differential Gene Expression in Canine Microdissected Anagen and Telogen Hair Follicles and Interfollicular Epidermis
- Monilethrix, a rare inherited hair shaft disorder in siblings
- Molecular mechanisms underlying cashmere quality differences between Jiangnan cashmere goats and Changthangi pashmina goats
- The polygenic architecture of hidradenitis suppurativa reveals signaling mechanisms that implicate epithelial remodeling
- Author response: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- 555 Dermal single-cell atlas: a novel tool to explore fibroblast heterogeneity
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing