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Research 661–690 of 1000+
- Primary cicatricial alopecia associated with systemic indolent mastocytosis
- Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology
- Identification of the Key Genes Associated with Different Hair Types in the Inner Mongolia Cashmere Goat
- Proof-of-Principle Study of Inflammasome Signaling Proteins as Diagnostic Biomarkers of the Inflammatory Response in Parkinson’s Disease
- Forensic approach in cases of anabolic-androgenic steroid abuse and cardiovascular mortality: insights from autopsy, histopathology, immunohistochemistry and toxicology
- 464 Spatial transcriptomics links gene expression profiles to functional and structural traits of darkly pigmented skin
- Faculty Opinions recommendation of Mapping the molecular and structural specialization of the skin basement membrane for inter-tissue interactions.
- Developing Patient-Derived 3D-Bioprinting models of pancreatic cancer
- Reduced SMAD2/3 activation independently predicts increased depth of human cutaneous squamous cell carcinoma
- Stem cells, organoids and their applications for human diseases: Special issue of BMB Reports in 2023
- Acute sensitivity of the oral mucosa to oncogenic <i>K‐ras</i>
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- The Genetic Architecture of Alopecia Areata
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Identification of an Intronic Regulatory Element Necessary for Tissue-Specific Expression of <i>Foxn1</i> in Thymic Epithelial Cells
- Recent advances in the molecular mechanisms causing primary generalized glucocorticoid resistance
- Androgen Affects the Inhibitory Avoidance Memory by Primarily Acting on Androgen Receptor in the Brain in Adolescent Male Rats
- Synthesis of porcine pCLCA2 protein during late differentiation of keratinocytes of epidermis and hair follicle inner root sheath
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- Exact, time-independent estimation of clone size distributions in normal and mutated cells
- Spatial and single-cell transcriptomics unravel the complex interplay between the body and medical implants
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Synthetically programmed antioxidant delivery by a domesticated skin commensal
- Variation in the ovine trichohyalin gene and its association with wool curvature
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response