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Research 30 of 1000+
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Skin barrier, phenotypic and genotypic characterisation of autosomal recessive ichthyosis in TGM1‐deficient Jack Russell Terriers and response to topical ceramide
- Forensic DNA phenotyping: a review on SNP panels, genotyping techniques, and prediction models
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Role of the Wnt signaling pathway in keratoacanthoma
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- What does acne genetics teach us about disease pathogenesis?
- 312 CRISPR/Cas9-based targeted genome editing for correction of recessive dystrophic epidermolysis bullosa using iPS cells
- 314 Molecular genetic dissection of ILVEN leads to successful targeted therapy
- 316 Specialized ribosomes in human dermal fibroblast senescence
- 313 Different polyamine levels in the vertex and occipital hair of pattern hair loss patients
- Cryptic Patterning of Avian Skin Confers a Developmental Facility for Loss of Neck Feathering
- Male-pattern baldness susceptibility locus at 20p11
- Carriers of 21-Hydroxylase Deficiency Are Not at Increased Risk for Hyperandrogenism*
- Cloning of the human phenol sulfotransferase gene family: three genes implicated in the metabolism of catecholamines, thyroid hormones and drugs
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- 9. Immunology and Genetics
- Resveratrol derivatives: a patent review (2009 – 2012)
- The genetic basis of dermatophytosis skin infection susceptibility
- Understanding Polycystic Ovary Syndrome
- The Rotterdam Study: 2018 update on objectives, design and main results
- EZH1 and EZH2 cogovern histone H3K27 trimethylation and are essential for hair follicle homeostasis and wound repair
- The Rotterdam Study: 2016 objectives and design update
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- SOX11 and SOX4 drive the reactivation of an embryonic gene program during murine wound repair
- Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans