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Research 91–120 of 1000+
- Shifting IRES versus Cap-initiated translation during homeostatic stem cell differentiation and stress
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Genetic architecture of mouse skin inflammation and tumour susceptibility
- Minoxidil Sulfotransferase Enzyme (SULT1A1) genetic variants predicts response to oral minoxidil treatment for female pattern hair loss
- Evidence for two independent functional variants for androgenetic alopecia around the androgen receptor gene
- SNP variation in male pattern hair loss in Russians with different dihydrotestosterone levels
- Plasma Zinc Levels in Males with Androgenetic Alopecia as Possible Predictors of the Subsequent Conservative Therapy’s Effectiveness
- Polycystic ovary syndrome: a complex condition with psychological, reproductive and metabolic manifestations that impacts on health across the lifespan
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- Facial skin aging: an integrative analysis of genetics, epigenetics, and lifestyle factors
- Association of Rs231775 Genetic Variant of Cytotoxic T-lymphocyte Associated Protein 4 with Alopecia Areata Disease in Males: A Case–Control Study
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta
- 312 CRISPR/Cas9-based targeted genome editing for correction of recessive dystrophic epidermolysis bullosa using iPS cells
- Precision therapeutics in non-scarring alopecia: a systemic genomic and pathway-based framework for targeted interventions
- 316 Specialized ribosomes in human dermal fibroblast senescence
- 313 Different polyamine levels in the vertex and occipital hair of pattern hair loss patients
- Follikelhormone
- Peroxisome Proliferator Activated Receptors Gamma Serum levels and Gene Polymorphism in Frontal Fibrosing Alopecia: A Case Control Study
- THE PATHOGENESIS OF ALOPECIA AREATA
- What does acne genetics teach us about disease pathogenesis?
- Associations between sun sensitive pigmentary genes and serum prostate specific antigen levels
- Global Landscapes of Human Phenotypic Variation in Inherited Traits
- Analysis of Vitamin D Receptor (VDR) Gene Polymorphisms in Alopecia Areata
- Risk factors for prostate cancer: a case-control study investigating selected key exposures and their interactions with predisposition genes
- Evidence-Based and Potential Benefits of Metformin in the Polycystic Ovary Syndrome: A Comprehensive Review
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient