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Research 271–300 of 1000+
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- Glucocorticoid Resistance Syndrome in 2 Patients With Diverse Genotype
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Novel insights into the molecular mechanisms underlying generalized glucocorticoid resistance and hypersensitivity syndromes
- Recent advances in the molecular mechanisms causing primary generalized glucocorticoid resistance
- Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report
- Werewolf, there wolf: variants in <i>Hairless</i> associated with hypotrichia and roaning in the lykoi cat breed
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- SPT6 maintains epidermal homeostasis by inhibiting an NF-κB-positive feedback loop to prevent excessive inflammation
- 8242 A Case of Ayme Gripp Syndrome
- Wound Healing Efficacy of Cellulose Hydrogel on ICR Mice: A Morphoanatomical, Histological and Genomic Study
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Ichthyosiform Erythroderma, a Multifaceted Syndromic Entity
- Pathogenesis and clinical features of alopecia in epidermolysis bullosa: A systematic review
- A mouse with bad hair and poor taste
- Single‐cell transcriptomic analysis of small and large wounds reveals the distinct spatial organization of regenerative fibroblasts
- Isolation ofStaphylococcus simulansfrom Dermatitis in a Captive African Pygmy Hedgehog
- Pseudallescheria boydii infection associated with IgG4-related disease
- A blistering child: sudden erythema with blisters in a sick girl
- Post SARS-CoV-2 vaccination effluvium
- Comparative Skin Transcriptomics Reveals Key Regulators of Cashmere Fiber Production in Inner Mongolian Goats
- Hypomyelinating leukodystrophy-10 presenting with an additional atypical feature of increased body hair and Mongolian spots
- Dermatological diseases from a genetic perspective
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Defining the identity of mouse embryonic dermal fibroblasts
- URB expression in human dermal papilla cells
- Transcriptome profiling of whisker follicles in methamphetamine self-administered rats
- 0977 Pathogenic hallmarks of primary lymphocyte-mediated scarring alopecia revealed by single nuclear and spatial multiomics