Search
for
Sort by
Research 301–330 of 1000+
- 5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A review
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: Oral Presentations
- FGF5 is a crucial regulator of hair length in humans
- Structural insights into SARS-CoV-2 spike protein and its natural mutants found in Mexican population
- Hair Follicle Disruption Facilitates Pathogenesis to UVB-Induced Cutaneous Inflammation and Basal Cell Carcinoma Development in Ptch+/− Mice
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
- Transcriptome Meta-Analysis Confirms the Hidradenitis Suppurativa Pathogenic Triad: Upregulated Inflammation, Altered Epithelial Organization, and Dysregulated Metabolic Signaling
- A kindred with mutant IKAROS and autoimmunity
- An essential role for <i>Rxrα</i> in the development of Th2 responses
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- Hair follicle regeneration suppresses Ras-driven oncogenic growth
- Suppression of FGF5 and FGF18 Expression by Cholesterol-Modified siRNAs Promotes Hair Growth in Mice
- Pinkie, the First Viable Germline Hypomorph Allele of Retinoid X Receptor Alpha, Reveals an Important Role for RXRa in Th2 Development.
- Erythrodermic Psoriasis in the Context of Emerging Triggers: Insights into Dupilumab-Associated and COVID-19-Induced Psoriatic Disease
- Tinea capitis caused by Trichophyton violaceum in an immunocompetent elderly patient: a case report and review of literature
- Loss of adipocyte phospholipase gene PLAAT3 causes lipodystrophy and insulin resistance due to inactivated arachidonic acid-mediated PPARγ signaling
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Recently Identified Forms of Epidermolysis Bullosa
- HPV8 Field Cancerization in a Transgenic Mouse Model Is due to Lrig1+ Keratinocyte Stem Cell Expansion
- The secret identities of TMPRSS2: Fertility factor, virus trafficker, inflammation moderator, prostate protector and tumor suppressor
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Experimental cutaneous Bacillus anthracis infections in hairless HRS/J mice
- <i>In vivo</i> alteration of the keratin 17 gene in hair follicles by oligonucleotide‐directed gene targeting
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- 307 Phenotypic-genotypic expansion of plectinopathy in a patient with muscular dystrophy and immune-mediated myasthenia gravis
- Rabson-Mendenhall syndrome: two case reports and a brief review of the literature