Search
for
Sort by
Research 151–180 of 1000+
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Melanocyte and gonad activity as potential severity modifying factors in C3H/HeJ mouse alopecia areata
- Developmental genetics of color pattern establishment in cats
- PCOS: update and diagnostic approach
- DNA phenotyping: current application in forensic science
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Genetic Variants and Protective Immunity against SARS-CoV-2
- COVID-19: The question of genetic diversity and therapeutic intervention approaches
- Acne
- Debatable Topics in PCOS Patients
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- The Polycystic Ovary Syndrome - Challenges and Opportunities in Adolescent Medicine
- Global Landscapes of Human Phenotypic Variation in Inherited Traits
- Human Pigmentation: A Review of Molecular Mechanisms, Genetic Architecture, Evolution, Forensic DNA Phenotyping and Health Implications
- Research progress on mechanisms of skin aging and anti-aging strategies
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- Androgenetska alopecija u žena
- Nociceptive and Nonnociceptive Roles of TRPV3 and Its “Druggability”
- The Basic Science of Hair Biology
- Weakly supervised learning of biomedical information extraction from curated data
- Genetic Disorders and Defects in Vitamin D Action
- Androgen Signaling Regulates SARS-CoV-2 Receptor Levels and Is Associated with Severe COVID-19 Symptoms in Men
- What causes hidradenitis suppurativa ?—15 years after
- Frontal Fibrosing Alopecia: An Update on Pathogenesis, Diagnosis, and Treatment
- An Overview of Alopecias
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne
- Alopecia in IL-10-deficient mouse pups is c-kit-dependent and can be triggered by iron deficiency
- Overexpression of alkaline phosphatase improves the hair-inductive capacity of cultured human dermal papilla spheres