Search
for
Sort by
Research 481–510 of 565
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Malignant Melanoma and Its Stromal Nonimmune Microecosystem
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- ‘Malignant melanoma microecosystem’: Immunohistopathological insights into the stromal cell phenotype
- Selenium Compounds and Their Bioactivities: Molecular Mechanisms and Prospects for Functional Food and Therapeutic Applications
- RAPID ALKALINIZATION FACTOR 22 is a key modulator of the root hair growth responses to fungal ethylene emissions in Arabidopsis
- Chemical and Bioactive Properties of Red Rice with Potential Pharmaceutical Use
- A newborn presenting with congenital blistering
- HR Gene Variants Identified in Mexican Patients with Alopecia Areata
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- CTLA4 +49AG (rs231775) and CT60 (rs3087243) gene variants are not associated with alopecia areata in a Mexican population from Monterrey Mexico
- Candidate Gene Analysis Of Alopecia Areata In Jordanian Population Of Arab Descent: A Case–Control Study
- Selection signatures for fiber production in commercial species: A review
- Retinoic acid exerts sexually dimorphic effects on muscle energy metabolism and function
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Case-Only Trees and Random Forests for Exploring Genotype-Specific Treatment Effects in Randomized Clinical Trials with Dichotomous End Points
- Ashwagandha root in the treatment of non-classical adrenal hyperplasia
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Prevalence and some risk factors with therapeutic trial of sheep dermatophytosis in Egypt
- Assessment of hair and cashmere properties and their genetic background of several goat breeds in Southwest China
- A Porcine Model for the Development and Testing of Preoperative Skin Preparations
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- The Dark Side of Gefitinib: Reflectance Confocal Microscopy Applied to Hair Hyperpigmentation
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Genetic prediction of male pattern baldness based on large independent datasets
- Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy