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Research 931–960 of 1000+
- An incompletely penetrant novel MAFB (p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal osteolysis syndrome
- The circular RNA circNlgnmediates doxorubicin-inducedcardiac remodeling and fibrosis
- Biochemical and Structural Characteristics, Gene Regulation, Physiological, Pathological and Clinical Features of Lipocalin-Type Prostaglandin D2 Synthase as a Multifunctional Lipocalin
- Thymic Mesenchymal Cells Have a Distinct Transcriptomic Profile
- Merkel cell carcinoma: updates in tumor biology, emerging therapies, and preclinical models
- β1 Integrins with Individually Disrupted Cytoplasmic NPxY Motifs Are Embryonic Lethal but Partially Active in the Epidermis
- The secret identities of TMPRSS2: Fertility factor, virus trafficker, inflammation moderator, prostate protector and tumor suppressor
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies
- Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
- Converging physiological roles of the anthrax toxin receptors
- Rapamycin but not acarbose decreases age-related loss of outer hair cells in the mouse Cochlea
- Novel insights into the molecular mechanisms underlying generalized glucocorticoid resistance and hypersensitivity syndromes
- Recent advances in the molecular mechanisms causing primary generalized glucocorticoid resistance
- Thymosin Beta-4 Induces Mouse Hair Growth
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Gene network analysis reveals candidate genes related with the hair follicle development in sheep
- Basal cell carcinomas acquire secondary mutations to overcome dormancy and progress from microscopic to macroscopic disease
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
- Multiomics global landscape of stemness-related gene clusters in adipose-derived mesenchymal stem cells
- Role of anabolic agents in colorectal carcinogenesis: Myths and realities (Review)
- Female pattern hair loss—An update
- Oil body bound oleosin-rhFGF9 fusion protein expressed in safflower (Carthamus tinctorius L.) stimulates hair growth and wound healing in mice
- A human vitamin D receptor mutation causes rickets and impaired Th1/Th17 responses
- Acute sensitivity of the oral mucosa to oncogenic <i>K‐ras</i>
- The Fate of Epidermal Tight Junctions in the stratum corneum: Their Involvement in the Regulation of Desquamation and Phenotypic Expression of Certain Skin Conditions
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- SOX9 in organogenesis: shared and unique transcriptional functions