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- A Clinical Genetics-Driven Dual Diagnosis of Prader–Willi Syndrome Due to Mosaic Maternal UPD(15) and NOTCH3-Related CADASIL
- Part 1. Genetic pathway of maternal transmission in Topiramate-treated zebrafish modelPart 2.Effects of herbal medicine on zebrafish embryos
- Supplementary Material for: Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- Supplementary Material for: Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Alopecia Areata in a Pediatric Patient with Delayed Maternal Manifestation: A Case Report
- Regional Differences in Dorsal Skin Determine the Rate of Adhesive Material-Induced Hair Regeneration
- A comprehensive review of the medical and cosmetic applications of exosomes in dermatology
- Editorial: Advances in reproductive biotechnologies in carnivores
- Molecular Mechanisms Responsible for Therapeutic Potential of Mesenchymal Stem Cell-Derived Secretome
- Alopecia in IL-10-deficient mouse pups is c-kit-dependent and can be triggered by iron deficiency
- Reciprocal effects suggest maternal and extranuclear influences on fruit traits in winter squash breeding
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- Prenatal diagnosis of a fetus harboring an intermediate load of the A3243G mtDNA mutation in a maternal carrier diagnosed with MELAS syndrome
- Fine mapping of the human <i>AR/EDA2R</i> locus in androgenetic alopecia
- Supplementary Material for: Case report - Hair shaft normalization and hair growth in SPINK5-syndromic epidermal differentiation disorder (Netherton syndrome) while on treatment with dupilumab: a novel therapeutic approach for Trichorrhexis invaginata
- Supplementary Material for: Case report - Hair shaft normalization and hair growth in SPINK5-syndromic epidermal differentiation disorder (Netherton syndrome) while on treatment with dupilumab: a novel therapeutic approach for Trichorrhexis invaginata
- Comparison of the effectivity of different snare types for collecting and retaining hair from Eurasian Lynx (Lynx lynx)
- Supplementary Material for: Plasma proteome–driven identification of druggable immune regulators of alopecia areata, validated by transcriptome and single-cell mapping
- Supplementary Material for: Plasma proteome–driven identification of druggable immune regulators of alopecia areata, validated by transcriptome and single-cell mapping
- A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders
- Supplementary Material for: Polymorphic CAG Repeat Numbers in the Androgen Receptor Gene of Female Pattern Hair Loss in a Han Chinese Population
- Fetal Programming of Polycystic Ovary Syndrome by Androgen Excess: Evidence from Experimental, Clinical, and Genetic Association Studies
- High Frequency of Symptomatic Zinc Deficiency in Infants in Northern Ethiopia
- Female Pattern Hair Loss: An Overview with Focus on the Genetics
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: Oral Presentations
- Engineering Cell Surfaces with Polyelectrolyte Materials for Translational Applications
- A young male with kidney damage from genetic mitochondrial disease: case report and literature review
- Molecular epidemiology of hypospadias: Review of genetic and environmental risk factors