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Research 271–300 of 1000+
- Evolution in action: highlighting a role for the Agouti gene in development?
- Amino acid–derived defense metabolites from plants: A potential source to facilitate novel antimicrobial development
- COVID-19: The question of genetic diversity and therapeutic intervention approaches
- 312 CRISPR/Cas9-based targeted genome editing for correction of recessive dystrophic epidermolysis bullosa using iPS cells
- 316 Specialized ribosomes in human dermal fibroblast senescence
- 313 Different polyamine levels in the vertex and occipital hair of pattern hair loss patients
- A Clinical Approach to Severe Insulin Resistance
- Acne
- LO-010 Relationship between the EULAR/ACR classification criteria and organ damage in systemic lupus erythematosus
- Cyclosporine-Induced Alopecia in Childhood Nephrotic Syndrome – A Case Report
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- Hair Follicle Immune Privilege Revisited: The Key to Alopecia Areata Management
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Alymphoid cystic thymic dysgenesis - FOXN1 gene mutation: a rare case report of two siblings
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Replicative stress, stem cells and aging
- Androgen receptor gene polymorphism and polycystic ovary syndrome
- The diagnosis of nonclassic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, based on serum basal or post-ACTH stimulation 17-hydroxyprogesterone, can lead to false-positive diagnosis
- Novel<i>PAX</i><i>9</i>mutation associated with syndromic tooth agenesis
- A functional polymorphism in interleukin-1α (IL1A) gene is associated with risk of alopecia areata in Chinese populations
- The hair shaft: normality, abnormality, and genetics
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Interaction between estrogens and androgen receptor genes microsatellites, prostate-specific antigen and androgen receptor expressions in breast cancer
- Ischemic Stroke in a Young Adult Male During Finasteride Therapy
- Dermoscopy — 4th Conference of the Section of Dermoscopy and Other Skin Imaging Techniques (DiTOS) of the Polish Dermatological Society — Abstracts
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- The alopecia areata phenotype is induced by the water avoidance stress test in <i>cchcr1</i>-deficient mice
- WNT10B (wingless-type MMTV integration site family)
- Genetic Defects of Female Sexual Differentiation
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family