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Research 331–360 of 1000+
- Hedgehog Signaling in Papillary Fibroblasts Is Essential for Hair Follicle Regeneration during Wound Healing
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- GWASs Identify Genetic Loci Associated with Human Scalp Hair Whorl Direction
- Assessment of hair and cashmere properties and their genetic background of several goat breeds in Southwest China
- Skin regional specification and higher-order <i>HoxC</i> regulation
- Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Combined Systemic and Cutaneous Ovalbumin–Aluminum Sensitization Triggers Thermal Hyperalgesia, Spinal Gliosis, and Nociceptive Nerve Fibers Sprouting in Mice
- The Multifaceted Functions of TRPV4 and Calcium Oscillations in Tissue Repair
- Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
- Acne Syndromes and Mosaicism
- Hirsutism Beyond PCOS: Genome-wide Evidence for Genetic Factors
- IRF2BP2 genes provide new insights into coat type and fiber composition variation in sheep
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- Discovery of Four New<em> FGF5</em> Variants Causing Long Hair in the Dog
- The Effects of Spermidine on Functional and Transcriptomic Markers in Human Primary Keratinocytes
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- Dietary and Genetic Aspects of Polycystic Ovary Syndrome (PCOS) in Polish Women-Part II: Association of
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- Chemotherapy-Induced Alopecia by Docetaxel: Prevalence, Treatment and Prevention
- Skin barrier, phenotypic and genotypic characterisation of autosomal recessive ichthyosis in TGM1‐deficient Jack Russell Terriers and response to topical ceramide
- Association between PITX2 polymorphism and androgenetic alopecia in the Indian population
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient
- Plant elicitor Peptides regulate root hair development in Arabidopsis
- The Opioid Receptor Influences Circadian Rhythms in Human Keratinocytes through the β-Arrestin Pathway
- Cutaneous Manifestations in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED): A Comprehensive Review