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Research 691–720 of 1000+
- Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing
- <i>BUZZ</i>: an essential gene for postinitiation root hair growth and a mediator of root architecture in <i>Brachypodium distachyon</i>
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- Author response: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- 130 Expression of nidogen1 in basal cell carcinoma
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex
- Cyberspace Chat
- NUDT15 R139C-related thiopurine leukocytopenia is mediated by 6-thioguanine nucleotide-independent mechanism in Japanese patients with inflammatory bowel disease
- The L412F variant of Toll-like receptor 3 (TLR3) is associated with cutaneous candidiasis, increased susceptibility to cytomegalovirus, and autoimmunity
- Exomic Sequencing of Immune-Related Genes Reveals Novel Candidate Variants Associated with Alopecia Universalis
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- Reclassification of Botryococcus braunii chemical races into separate species based on a comparative genomics analysis
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Genome-Wide Association Study of Alopecia Areata in Taiwan: The Conflict Between Individuals and Hair Follicles
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- PA33 When bones speak through nails: insights from a paediatric case series
- Trichoscopy in Unveiling the Triad of Netherton Syndrome
- P-18 THREE BODY PROBLEM PATIENT: EHLER DANLOS SYNDROME COMBINED WITH HYPOPHOSPHATASIA AND FATTY ACID OXIDATION DEFECT
- Angiogenesis and Microcirculation in Ischemic Heart Disease
- Ethnopharmacology and hair: Indian perspectives
- Editorial Comment
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- IRF2BP2 genes provide new insights into coat type and fiber composition variation in sheep
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- What Ages Hair?
- Third International Research Workshop on Alopecia Areata
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Laminin 332 Is Indispensable for Homeostatic Epidermal Differentiation Programs