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Research 211–240 of 1000+
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Immunosenescence and inflammaging in Parkinson’s disease: mechanisms and therapeutic prospects
- A State-of-the-Art Overview on (Epi)Genomics and Personalized Skin Rejuvenating Strategies
- Reshaped DNA methylation cooperating with homoeolog‐divergent expression promotes improved root traits in synthesized tetraploid wheat
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Forensic DNA Phenotyping
- In This Issue
- Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
- Tooth Development Associated with Mutations in Hereditary Vitamin D–Resistant Rickets
- Global trends in tertiary lymphoid structures: a bibliometric analysis from 2014 to 2023
- An adolescent girl presenting with primary amenorrhea: A case report of complete androgen insensitivity syndrome
- A Machine Learning-Based Scalp Hair Inspection and Diagnosis System for Scalp Health
- Improving human forensics through advances in genetics, genomics and molecular biology
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Genetic Variants and Protective Immunity against SARS-CoV-2
- In vivo expression of VCAM1 precedes nephron loss following kidney tubular necrosis
- Abstracts
- Machine learning for nanozyme development in anti‐inflammatory applications
- Establishing an Evidence-Based System for Cosmetic Safety and Efficacy Evaluation
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient
- Five cluster classifications of long COVID and their background factors: A cross-sectional study in Japan
- Current Guidelines for Diagnosing PCOS
- The Vitamin D Receptor Is a Wnt Effector that Controls Hair Follicle Differentiation and Specifies Tumor Type in Adult Epidermis
- Understanding the role of prostaglandin E2 in regulating human platelet activity in health and disease
- Hedgehog signaling reprograms hair follicle niche fibroblasts to a hyper-activated state
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Characterization of Clinical Features of Hospitalized Patients Due to the SARS-CoV-2 Infection in the Absence of Comorbidities Regarding the Sex: An Epidemiological Study of the First Year of the Pandemic in Brazil
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family