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Research 541–570 of 1000+
- 712 Using scanning electron microscopy to elucidate the role of hair shaft malformation in the pathogenesis of Central Centrifugal Cicatricial Alopecia
- Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments
- Shedding light on cashmere goat hair follicle biology: from morphology analyses to transcriptomic landascape
- Single-Cell Transcriptome Sequence Profiling on the Morphogenesis of Secondary Hair Follicles in Ordos Fine-Wool Sheep
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- Comprehensive transcriptome and methylome analysis delineates the biological basis of hair follicle development and wool-related traits in Merino sheep
- Identification of lncRNAs involved in the hair follicle cycle transition of cashmere goats in response to photoperiod change
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- Transcriptomic analyses of regenerating adult feathers in chicken
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Metabolic syndrome — a new definition and management guidelines
- Modeling animal genomics in mice: An authentic approach for the functional interrogation of evolutionarily and agriculturally critical variants
- Polycystic Ovarian Syndrome
- CPC14 Blaschko-linear trichoepitheliomas: unveiling type 1 segmental mosaicism
- Pangenome and genome variation analyses of pigs unveil genomic facets for their adaptation and agronomic characteristics
- Whole-Genome Resequencing Reveals Selection Signal Related to Sheep Wool Fineness
- Author response: Spatiotemporal dynamics of PIEZO1 localization controls keratinocyte migration during wound healing
- Epidermal Notch signalling: differentiation, cancer and adhesion
- Identification of reptilian genes encoding hair keratin-like proteins suggests a new scenario for the evolutionary origin of hair
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Research Relevant Conditions and Pathology in Nonhuman Primates
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- Molecular stratification of the human fetal vaginal epithelium by spatial transcriptome analysis
- SLE classification criteria item relationships: implications on SLE as a disease entity
- Dynamics and Epigenetics of the Epidermal Differentiation Complex
- Hair & Cutaneous Development
- Integration Analysis of Transcriptome Sequencing and Whole-Genome Resequencing Reveal Wool Quality-Associated Key Genes in Zhexi Angora Rabbits
- Male polycystic ovarian syndrome phenotype: a meta-analysis of endocrine-metabolic dysregulation in fathers and brothers of PCOS-affected women
- Aging in the sebaceous gland