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Research 391–420 of 1000+
- Skin Keratins
- The Rotterdam Study: 2016 objectives and design update
- Who Am I? Eyebrow Follicles Minimize Donor-Derived DNA for Germline Testing After Hematopoietic Stem Cell Transplantation
- A case of primary cutaneous natural killer/T-cell lymphoma, nasal type, with indolent clinical course: monoclonal expansion of Epstein-Barr virus genome correlating with the terminal aggressive behaviour
- Synthetically programmed antioxidant delivery by a domesticated skin commensal
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- Application of multi-omics techniques to androgenetic alopecia: Current status and perspectives
- LB788 Development of a novel three-dimensional human epidermal model from plucked hair follicle-derived keratinocytes
- In search of decoding the syntax of the bioelements in human hair – A critical overview
- Genome-Wide Associations with Body and Fleece Weight in United States Sheep
- Berardinelli–Seip syndrome
- From bedside to bench: regulation of host factors in SARS-CoV-2 infection
- Genome-wide association study of atopic and autoimmune comorbidities in alopecia areata
- The color of human hair
- Genomic Organization and Amplification of the Human Keratin 15 and Keratin 19 Genes
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Molecular monitoring of short- and long-term transcriptional effects of hair growth stimulating agents
- Causal associations between plasma proteins and prostate cancer: a Proteome-Wide Mendelian Randomization
- Identification of Familial Infections Using Multilocus Microsatellite Typing in Tinea Corporis due to <i>Microsporum canis</i>
- Metabolic disease with autoimmune phenomena: 2 cases of SLE-like disease in young children diagnosed with lysinuric protein intolerance
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Genomic Surveillance Reveals the Rapid Expansion of the XBB Lineage among Circulating SARS-CoV-2 Omicron Lineages in Southeastern Wisconsin, USA
- Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Author response: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Identification of genes and proteins associated with anagen wool growth
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- Genome-Wide Association Studies of Hair Whorl in Pigs
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata