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Research 331–360 of 494
- Towards Defining the Pathogenesis of the Hairless Phenotype
- Apoptosis resistance in peripheral blood lymphocytes of alopecia areata patients
- Lanceolate hair-J (<i>lah<sup>J</sup> </i> ): A mouse model for human hair disorders
- Rare and common genetic determinants of metabolic individuality and their effects on human health
- The mouse frizzy (<i>fr</i>) and rat ‘hairless’ (<i>fr</i><sup><i>CR</i></sup>) mutations are natural variants of protease serine S1 family member 8 (<i>Prss8</i>)
- Genetically separable determinants of hair keratin gene expression
- Clinical uses for calciotropic hormones 1,25-dihydroxyvitamin D3 and parathyroid hormone-related peptide in dermatology: a new perspective.
- Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart
- Insertional mutation of the hairless locus on mouse Chromosome 14
- Age-Related Changes in Hair Shaft Protein Profiling and Genetically Variant Peptides
- Male and female pattern hair loss: Treatable and worth treating
- Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis
- The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Mesenchymal Stem Cells With Modification of Junctional Adhesion Molecule A Induce Hair Formation
- HR Gene Variants Identified in Mexican Patients with Alopecia Areata
- Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy
- Hair Follicle-Related MicroRNA-34a Serum Expression and rs2666433A/G Variant in Patients with Alopecia: A Cross-Sectional Analysis
- Osteopontin Gene Polymorphisms rs1126616 C>T and rs1126772 A>G are Associated with Atopic Dermatitis in Polish Population
- Case report: Two individuals with AEBP1-related classical-like EDS: Further clinical characterisation and description of novel AEBP1 variants
- Expanding the Cutaneous Spectrum of Nicolaides‑Baraitser Syndrome: Eczema and Generalized Hair Loss
- Decision letter: Live imaging reveals chromatin compaction transitions and dynamic transcriptional bursting during stem cell differentiation in vivo
- Role of <i>foxn1</i> in <i>Xenopus laevis</i> thymopoiesis.
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Hair Anomalies in a 6-Year-Old Girl
- Lanceolate hair-J (lahJ): a mouse model for human hair disorders [In Process Citation]
- A Ca <sup>2+</sup> /calmodulin-dependent protein kinase required for symbiotic nodule development: Gene identification by transcript-based cloning
- Vaccines, adjuvants and autoimmunity
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- The Rotterdam Study: 2010 objectives and design update