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Research 661–690 of 1000+
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- The Roles of Keratinocytes in the Initiation, Progression and Maintenance of Hidradenitis Suppurativa
- Two novel MBTPS2 missense mutations impairing S2P proteolytic activity lead to IFAP syndrome with new phenotypic anomalies
- Clinical Snippets
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Adrenoleukodystrophy: A Rare Case Report
- P78 Acrodermatitis enteropathica in children: clinical cases
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Genosomes: An introspection into transfection, future perspectives and applications
- Advances in single-cell transcriptomics in animal research
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Analysis of Vitamin D Receptor (VDR) Gene Polymorphisms in Alopecia Areata
- <i>Ashtanindita</i> <i>Purusha</i> – The Clinical Revelation : A Review
- Comparison of Alopecia areata in Human and Nonhuman Mammalian Species
- Hair follicle stem cell replication stress drives IFI16/STING-dependent inflammation in hidradenitis suppurativa
- Papillon-Lefévre Syndrome: A Rare Case Report and a Brief Review of Literature
- Current systemic treatment strategies for hidradenitis suppurativa
- FOXN1 deficient nude severe combined immunodeficiency
- It’s X-Related: Biological Bases of Increased COVID-19 Morbidity and Mortality in Men
- Understanding the molecular basis of mesenchymal stem cell stemness: implications for clinical applications
- From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?
- 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
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- A Small Deletion Hotspot in the Type II Keratin Gene<i>mK6irs1/Krt2-6g</i>on Mouse Chromosome 15, a Candidate for Causing the Wavy Hair of the Caracul (<i>Ca</i>) Mutation
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Identification of somatic and germline mosaicism for a keratin 5 mutation in epidermolysis bullosa simplex in a family of which the proband was previously regarded as a sporadic case
- Role of Aire and Notch4 Allelic Mutations in Alopecia Areata in C3H/HeJ Mice
- Psoriasis and Related Disorders
- Advances in Vitiligo Treatment
- The polygenic architecture of hidradenitis suppurativa reveals signaling mechanisms that implicate epithelial remodeling