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Research 301–330 of 1000+
- Androgen modulation of Wnt/β-catenin signaling in androgenetic alopecia
- Treatment options for alopecia: an update, looking to the future
- MicroRNA in skin diseases
- Whole Genome Scan and Selection Signatures for Climate Adaption in Yanbian Cattle
- The Genetics of Human Skin Disease
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- The effect of plasma rich in growth factors combined with follicular unit extraction surgery for the treatment of hair loss: A pilot study
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- DNA phenotyping: current application in forensic science
- Predicting Human Appearance from DNA for Forensic Investigations
- The Polycystic Ovary Syndrome - Challenges and Opportunities in Adolescent Medicine
- Association of Cyp11a Gene with Polycystic Ovarian Syndrome Patients in Lahore, Pakistan
- Follikelhormone
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- Lower prostate cancer risk in Swedish men with the androgen receptor E213 A-allele
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Sulforaphane mobilizes cellular defenses that protect skin against damage by UV radiation
- Steroid Biomarkers and Genetic Studies Reveal Inactivating Mutations in Hexose-6-Phosphate Dehydrogenase in Patients with Cortisone Reductase Deficiency
- AGD1, a class 1 ARF‐GAP, acts in common signaling pathways with phosphoinositide metabolism and the actin cytoskeleton in controlling Arabidopsis root hair polarity
- Sulphation catalysed by the human cytosolic sulphotransferases - chemical defence or molecular terrorism?
- TCL1 transgenic mouse model as a tool for the study of therapeutic targets and microenvironment in human B-cell chronic lymphocytic leukemia
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Acne
- Medications
- Abstracts
- ESGCT and FSGT Collaborative Congress Helsinki, Finland September 17–20, 2015 Abstracts
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Disease causing homozygous variants in the human hairless gene
- Polycystic ovary syndrome: etiology, pathogenesis and diagnosis