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Research 541–570 of 1000+
- Description of clinical aspects and microscopy of the hair shaft of a carrier of familial monilethrix
- Whole-transcriptome RNA sequencing reveals global expression dynamics and ceRNA regulatory networks related to hair follicle development and melanogenesis in goats
- The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits
- Role of Csdc2 in Regulating Secondary Hair Follicle Growth in Cashmere Goats
- Genome-wide association study reveals candidate genes associated with body weight and wool traits in Ordos fine-wool sheep
- Comparative Skin Transcriptomics Reveals Key Regulators of Cashmere Fiber Production in Inner Mongolian Goats
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Genome-Wide Association Studies of Hair Whorl in Pigs
- Investigating RNA-Seq-based differential gene expression during hair follicle development in Angora goat skin
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia
- Wound Healing: A Cellular Perspective
- Generalized atrophic benign epidermolysis bullosa.
- Multiomics-empowered Deep Phenotyping of Ulcerative Colitis Identifies Biomarker Signatures Reporting Functional Remission States
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- IRF2BP2 genes provide new insights into coat type and fiber composition variation in sheep
- miR-200a Targets PITX2 to Mediate Goose Fibroblast Proliferation Through the Wnt Pathway
- The evaluation of IL-4 VNTR intron 3 and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with alopecia areata: a case–control study
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Goat Genomic Resources: The Search for Genes Associated with Its Economic Traits
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- Deletion of an Enhancer in FGF5 is Associated With Ectopic Expression in Goat Hair Follicles and the Cashmere Growth Phenotype
- Alopecia Areata
- Author response: Structural basis of malodour precursor transport in the human axilla
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- Making the head: Caspases in life and death
- An Update of Congenital Adrenal Hyperplasia
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family