Search
for
Sort by
Research 301–330 of 450
- Efficacy of 0.1% adapalene in a non-inflammatory Kyoto Rhino Rat acne model
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Recessive Epidermolysis Bullosa Simplex Phenotype Reproduced in Vitro
- Epithelial elements in superficial angiomyxomas: mimicry of adnexal development, and mesenchymal‐to‐epithelial transition
- Corneodesmosomes and corneodesmosin: from the stratum corneum cohesion to the pathophysiology of genodermatoses
- Successful Treatment of Alopecia Areata with Topical Calcipotriol
- The impact of VDR expression and regulation in vivo
- Hairless down-regulates expression of Msx2 and its related target genes in hair follicles
- Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Atypical presentation of Acrodermatitis enteropathica in a child: later onset with life-threatening severe extensive dermatitis and septic shock
- Biomedical applications of organoids in genetic diseases
- FilaggrinHigh melanomas exhibit active FGFR and allergic signatures with impaired GNA14 and Th1 signatures
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- 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
- Apoptotic dysregulation mediates stem cell competition and tissue regeneration
- The molecular basis of human keratin disorders
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Hair Defects and Pup Loss in Mice with Targeted Deletion of the First Cut Repeat Domain of theCux/CDPHomeoprotein Gene
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Foxn1 in Skin Development, Homeostasis and Wound Healing
- Identification of an Intronic Regulatory Element Necessary for Tissue-Specific Expression of <i>Foxn1</i> in Thymic Epithelial Cells
- Cyclic Alopecia and Abnormal Epidermal Cornification in Zdhhc13 -Deficient Mice Reveal the Importance of Palmitoylation in Hair and Skin Differentiation
- CRISPR/Cas9-mediated Disruption of Fibroblast Growth Factor 5 in Rabbits Results in a Systemic Long Hair Phenotype by Prolonging Anagen
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Comparison of the acute ultraviolet photoresponse in congenic albino hairless C57BL/6J mice relative to outbred SKH1 hairless mice
- Differential expression of KRT83 regulated by the transcript factor CAP1 in Chinese Tan sheep
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population