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Research 571–600 of 705
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Evaluation and treatment of facial feminization surgery: part I. forehead, orbits, eyebrows, eyes, and nose
- Rapamycin but not acarbose decreases age-related loss of outer hair cells in the mouse Cochlea
- Restoration of Spermatogenesis and Male Fertility Using an Androgen Receptor Transgene
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Efficacy of metformin therapy in adolescent girls with androgen excess: relation to sex hormone–binding globulin and androgen receptor polymorphisms
- Iron Deficiency in Menstruating Adult Women: Much More than Anemia
- Treatment of Cystathionine β-Synthase Deficiency in Mice Using a Minicircle-Based Naked DNA Vector
- Genome-wide Target Enrichment-aided Chip Design: a 66 K SNP Chip for Cashmere Goat
- Laminin-511, inducer of hair growth, is down-regulated and its suppressor in hair growth, laminin-332 up-regulated in chemotherapy-induced alopecia
- Androgen Receptor Copy Number Variation and Androgenetic Alopecia: A Case-Control Study
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- The heme-responsive PrrH sRNA regulates <i>Pseudomonas aeruginosa</i> pyochelin gene expression
- A conditional multi-trait sequence GWAS discovers pleiotropic candidate genes and variants for sheep wool, skin wrinkle and breech cover traits
- Papillon–Lefèvre Syndrome: A Rare Case Report of Two Brothers and Review of the Literature
- A pair of transmembrane receptors essential for the retention and pigmentation of hair
- Genetics of Wool and Cashmere Fibre: Progress, Challenges, and Future Research
- Developmental and evolutionary comparative analysis of a regulatory landscape in mouse and chicken
- The Complexity of the Ovine and Caprine Keratin-Associated Protein Genes
- The protease corin regulates electrolyte homeostasis in eccrine sweat glands
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis
- <i>Pseudomonas aeruginosa</i> heme metabolites biliverdin IXβ and IXδ are integral to lifestyle adaptations associated with chronic infection
- Sox2 in the dermal papilla regulates hair follicle pigmentation
- Epigenetic Effects of Gender-Affirming Hormone Treatment: A Pilot Study of the ESR2 Promoter’s Methylation in AFAB People
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Synthetically programmed antioxidant delivery by a domesticated skin commensal