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Research 601–630 of 1000+
- Cellular senescence in skin‐related research: Targeted signaling pathways and naturally occurring therapeutic agents
- The role of WNT10B in physiology and disease: A 10-year update
- Regulatory T cells in skin mediate immune privilege of the hair follicle stem cell niche
- Regulatory pathway analysis of coat color genes in Mongolian horses
- <i>Pseudomonas aeruginosa</i> heme metabolites biliverdin IXβ and IXδ are integral to lifestyle adaptations associated with chronic infection
- Construction of the coexpression network involved in the pathogenesis of thyroid eye disease via bioinformatics analysis
- Integration of Point-of-Care Technology in the Decoding Process of Single Nucleotide Polymorphism for Healthcare Application †
- Obesity in Adults: Position Statement of Polish Association for the Study on Obesity, Polish Association of Endocrinology, Polish Association of Cardiodiabetology, Polish Psychiatric Association, Section of Metabolic and Bariatric Surgery of the Association of Polish Surgeons, and the College of Family Physicians in Poland
- Hair Pores Caused by Surfactants via the Cell Membrane Complex and a Prevention Strategy through the Use of Cuticle Sealing
- Does Complement Have a Role in the Pathogenesis of Alopecia Areata?
- Genetic analysis of 5 α reductase type 2 enzyme in relation to oxidative stress in cases of androgenetic alopecia in a sample of egyptian population
- A Mosaic Hotspot <i>PLCD1</i> Variant, Detectable in Blood‐Derived DNA, Associated With Nevus Trichilemmocysticus
- 한국인의 두피모발 특성과 남성형탈모증
- The New Keratin Nomenclature
- Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome
- A novel predictive model for the recurrence of pediatric alopecia areata by bioinformatics analysis and a single-center prospective study
- A comparative study of skin transcriptomes and histological observations for black and white hair colors of giant panda
- A recently characterized, underdiagnosed cause of female androgenetic alopecia and polycystic ovarian syndrome: non-classical 21 hydroxylase deficiency
- Transcriptional and epigenetic mechanisms governing epidermal stem cell regulation
- Androgenetic alopecia: An update
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Insertional mutation of the hairless locus on mouse Chromosome 14
- Mapping of a novel locus for keratosis follicularis squamosa on chromosome 7p14.3–7p12.1
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- A family of type I keratin genes and the homeobox-2 gene complex are closely linked to the rex locus on mouse chromosome 11
- A New Clinical Variant of Hereditary Localized Alopecia: Report of a Chinese Family Mapped to Chromosome 2p25.1–2p23.2