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Research 601–630 of 1000+
- Signaling pathways and targeted therapeutic strategies for polycystic ovary syndrome
- Abstracts from the 17th Congress of the European Society for Dermatology and Psychiatry
- The intragenic mRNA-microRNA regulatory network during telogen-anagen hair follicle transition in the cashmere goat
- Clinical review 74: Dermatological manifestations of endocrine disorders.
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Analyses of histological and transcriptome differences in the skin of short-hair and long-hair rabbits
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- The idiosyncratic genome of Korean long-tailed chicken as a valuable genetic resource
- Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
- Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa
- An incompletely penetrant novel MAFB (p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal osteolysis syndrome
- Overexpression of Nanog in amniotic fluid–derived mesenchymal stem cells accelerates dermal papilla cell activity and promotes hair follicle regeneration
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Variation in the Exon 3–4 Region of Ovine KRT85 and Its Effect on Wool Traits
- Bridging Personal and Population in Excitability Diseases: Will Studies of Rare Diseases Bring Generalizable Mechanisms From Monogenic Channelopathies?
- The L412F variant of Toll-like receptor 3 (TLR3) is associated with cutaneous candidiasis, increased susceptibility to cytomegalovirus, and autoimmunity
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Pmg-1 and Pmg-2 constitute a novel family of KAP genes differentially expressed during skin and mammary gland development
- CRISPR/Cas9-mediated Disruption of Fibroblast Growth Factor 5 in Rabbits Results in a Systemic Long Hair Phenotype by Prolonging Anagen
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- Mining Therapeutic Efficacy from Treasure Chest of Biodiversity and Chemodiversity: Pharmacophylogeny of Ranunculales Medicinal Plants
- Cell adhesion molecules in inflammatory and neoplastic skin diseases
- WRKY transcription factors (TFs): Molecular switches to regulate drought, temperature, and salinity stresses in plants
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Pulmonary manifestations of Birt-Hogg-Dubé syndrome
- Annotation of sheep keratin intermediate filament genes and their patterns of expression
- Beauty is skin deep: the fascinating biology of the epidermis and its appendages.
- Identification of two novel clusters of ultrahigh-sulfur keratin-associated protein genes on human chromosome 11