Search
for
Sort by
Research 361–390 of 1000+
- Síndrome postfinasterida y disfunción eréctil. Caso clínico y revisión de la literatura
- A Congenital Hair Defect: Trichoschisis With Alternating Birefringence and Low Sulfur Content
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- The biology and genetics of curly hair
- Transcriptome analysis reveals the genetic basis underlying the development of skin appendages and immunity in hedgehog (Atelerix albiventris)
- Machine learning driven multi-omics analysis of the genetic mechanisms behind the double-coat fleece formation in Hetian sheep
- Clinical and Genetic Aspects of Alopecia Areata: A Cutting Edge Review
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Hormonal and Genetic Etiology of Male Androgenetic Alopecia
- Detection of a Second KAP22 Family Member in Sheep and Analysis of Its Genetic Variation and Associations with Selected Wool Fibre Traits
- Resequencing Analyses Revealed Genetic Diversity and Selection Signatures during Rabbit Breeding and Improvement
- Expression of Desmoglein 1 Compensates for Genetic Loss of Desmoglein 3 in Keratinocyte Adhesion
- Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Evolution and genetic architecture of sex-limited polymorphism in cuckoos
- Androgenetic alopecia - just a cosmetic defect or a biomarker and risk factor for systemic diseases? - literature review
- https://researchopenworld.com/genetics-of-hidradenitis-suppurativa/#
- A young male with kidney damage from genetic mitochondrial disease: case report and literature review
- Ichthyosis with confetti: clinics, molecular genetics and management
- Biomedical applications of organoids in genetic diseases
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- MiR‐200c‐3p as a novel genetic marker and therapeutic tool for alopecia areata
- Tracking the Path of the Original: A Forensic Genetic, Demographic, and Legal Audit of the Muur Continuity Hypothesis
- Tracking the Path of the Original: A Forensic Genetic, Demographic, and Legal Audit of the Muur Continuity Hypothesis
- In Search of New Therapeutics—Molecular Aspects of the PCOS Pathophysiology: Genetics, Hormones, Metabolism and Beyond
- The Autoimmune Regulator (AIRE), Which Is Defective in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Patients, Is Expressed in Human Epidermal and Follicular Keratinocytes and Associates With the Intermediate Filament Protein Cytokeratin 17
- Follicular unit extraction combined with fractional carbon dioxide laser therapy for post‐traumatic eyebrow scar with defects: A prospective and comparative study
- Bone marrow-derived vasculogenesis leads to scarless regeneration in deep wounds with periosteal defects
- Role of Tissue Expander in Yemeni Post Burn Patients, Post Traumatic Scars, and Defects Management
- Activated Kras Alters Epidermal Homeostasis of Mouse Skin, Resulting in Redundant Skin and Defective Hair Cycling