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Research 541–570 of 762
- Association of Rs231775 Genetic Variant of Cytotoxic T-lymphocyte Associated Protein 4 with Alopecia Areata Disease in Males: A Case–Control Study
- Genetic correlation analysis does not associate male pattern baldness with COVID-19
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- 312 CRISPR/Cas9-based targeted genome editing for correction of recessive dystrophic epidermolysis bullosa using iPS cells
- Association of eNOS and STAT6 Gene Polymorphisms with the Susceptibility of Polycystic Ovary Syndrome in South Indian Women
- 316 Specialized ribosomes in human dermal fibroblast senescence
- 313 Different polyamine levels in the vertex and occipital hair of pattern hair loss patients
- Ускладнення у пацієнтів при трансплантації волосся
- Melatonin membrane receptors in peripheral tissues: Distribution and functions
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Sex differences in SARS-CoV-2 infection rates and the potential link to prostate cancer
- Inhibition of SARS-CoV-2 entry through the ACE2/TMPRSS2 pathway: a promising approach for uncovering early COVID-19 drug therapies
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Whole Genome Scan and Selection Signatures for Climate Adaption in Yanbian Cattle
- Cicatricial Alopecia Research Foundation meeting, May 2016: Progress towards the diagnosis, treatment and cure of primary cicatricial alopecias
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- Uncovering the complex relationship between balding, testosterone and skin cancers in men
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Genetic links between atopy, allergy, and alopecia areata: insights from a Mendelian randomization study
- Distinct Conditions Support a Novel Classification for Bradykinin-Mediated Angio-Oedema
- Collagen-Heparin-FGF2-VEGF Scaffolds Induce a Regenerative Gene Expression Profile in a Fetal Sheep Wound Model
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Physiology and Medical Treatments for Alopecia
- Genomic and transcriptomic landscape to decipher the genetic basis of hyperpigmentation in Lanping black-boned sheep (Ovis aries)
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- HSD3B1 gene polymorphism and female pattern hair loss in women with polycystic ovary syndrome
- Interconnected PolymerS TeChnology (IPSTiC): An Effective Approach for the Modulation of 5α-Reductase Activity in Hair Loss Conditions
- Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum