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Research 271–300 of 1000+
- Genetics of infertility and “assisted fertilization” in the Bible: The case of Abraham and his family
- Pharmacologic interventions in aging hair
- Integrated miRNA-mRNA analysis reveals regulatory pathways underlying the curly fleece trait in Chinese tan sheep
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- Eavesdropping on the conversation between immune cells and the skin epithelium
- Acne Syndromes and Mosaicism
- Selected abstracts from the 47th meeting of the Irish Endocrine Society Sligo, 24th & 25th November 2023
- Clinical, Biochemical and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Host-Directed FDA-Approved Drugs with Antiviral Activity against SARS-CoV-2 Identified by Hierarchical In Silico/In Vitro Screening Methods
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- An Update of Congenital Adrenal Hyperplasia
- Relative binding affinity of novel steroids to androgen receptors in hamster prostate
- Alopecia and its medical management
- 490 Samcyprone (diphenylcyclopropenone ointment) for the treatment of common warts
- GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk
- Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome
- Increased risk of chronic fatigue and hair loss following COVID-19 in individuals with hypohidrotic ectodermal dysplasia
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- The importance of basonuclin 2 in adult mice and its relation to basonuclin 1
- Post‐COVID-19 syndrome: assessment of short- and long-term post-recovery symptoms in recovered cases in Saudi Arabia
- Progress on genome-wide association studies and selection signature analysis for agronomic traits in Chinese sheep and goats: review
- Hair Loss in Systemic Disease
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- LEKTI: Netherton Syndrome and Atopic Dermatitis
- FOXN1 deficient nude severe combined immunodeficiency
- Trichoscopy as a diagnostic tool in trichorrhexis invaginata and Netherton syndrome