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- Identical p53 gene mutation in malignant proliferating trichilemmal tumour of the scalp and small cell carcinoma of the common bile duct: the necessity for therapeutic caution?
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Common variants in the sex hormone-binding globulin gene (SHBG) and polycystic ovary syndrome (PCOS) in Mediterranean women
- Common Variants in the Sex Hormone-Binding Globulin (SHBG) Gene Influence SHBG Levels in Women with Polycystic Ovary Syndrome
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Common pathologic pathways: A single prescription dream?
- Discrimination of Dysplastic Nevi from Common Melanocytic Nevi by Cellular and Molecular Criteria
- Rare and common genetic determinants of metabolic individuality and their effects on human health
- Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
- The inheritance of common baldness: Two B or not two B ?
- 199 Impairment of notch 1 signaling is a common defect in lesions from patients with hidradenitis suppurativa
- 965 In search of the common mechano-chemical pathways during the regeneration of spiny (acomys cahirinus) and laboratory (mus musculus) mouse skin
- Current insight into the functions of microRNAs in common human hair loss disorders: a mini review
- Dissection of genetic variation and evidence for pleiotropy in male pattern baldness
- The possible implication of the S250C variant of the autoimmune regulator protein in a patient with autoimmunity and immunodeficiency: in silico analysis suggests a molecular pathogenic mechanism for the variant
- Utilizing functional genomics approaches to characterize risk genes in alopecia areata
- Polymorphism of the Androgen Receptor Gene is Associated with Male Pattern Baldness
- Polymorphisms in androgen and estrogen receptor genes: effects on male aging
- Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation
- Adverse event reporting of four anti-Calcitonin gene-related peptide monoclonal antibodies for migraine prevention: a real-world study based on the FDA adverse event reporting system
- Investigations of 13 Genes in Non-Cicatricial Alopecia
- Faculty Opinions recommendation of Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.
- Faculty Opinions recommendation of Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.
- Studies on basal cell carcinoma with emphasis on the role of the human homologue of the Drosophila patched gene
- Gene-wide association study between the aromatase gene (<i>CYP19A1</i>) and female pattern hair loss
- 5 alpha-reductase-2 gene mutations in the Dominican Republic.
- Analysis of the human diseasome using phenotype similarity between common, genetic and infectious diseases
- Transglutaminase-3, an esophageal cancer-related gene
- Adverse events associated with aromatase inhibitors: an analysis of real-world datasets and drug-gene interaction network
- Faculty Opinions recommendation of Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.