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Research 271–300 of 1000+
- Uncovering the complex relationship between balding, testosterone and skin cancers in men
- Investigation of variants of the aromatase gene (CYP19A1) in female pattern hair loss
- Discovery of genes and proteins possibly regulating mean wool fibre diameter using cDNA microarray and proteomic approaches
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- SNP Markers: Analysis of Genetic Diversity and Identification of Genomic Regions in Pantaneiro Sheep and Texel Sheep Under Natural Selection
- Associations between genetically predicted sex and growth hormones and facial aging in the UK Biobank: a two−sample Mendelian randomization study
- Alopecia Areata and Alopecia Areata Incognita
- Precision-Based Management of Chronic Hair Fall: A Genomic-Guided Trichology Approach - A Case Analysis from Qatar
- Optimized Methodology to Produce Platelet-Rich Plasma and Perform Platelet Aggregation in Patients With Coronary Artery Disease
- Preparation and Physicochemical Evaluation of Topical Cream Ivermectin 1% for Treatment of Rosacea
- Alopecia Areata in 12 years old female treated with Oral Azathioprine: A case report and review
- Alopecia Areata
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Defining the identity of mouse embryonic dermal fibroblasts
- A new mutation resulting in the truncation of the TRAF6-interacting domain of XEDAR: a possible novel cause of hypohidrotic ectodermal dysplasia: Figure 1
- Finding bald spots on chromosome 20p11
- CPC12 Coinheritance of <i>BRCA2</i> and <i>CYLD</i> germline pathogenic variants associated with targetable metastatic malignant cylindroma
- 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
- A symphony of signals: the intricate role of lncRNAs in dermatological disorders
- Alopecia
- Novel<i>PAX</i><i>9</i>mutation associated with syndromic tooth agenesis
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia
- Treatment options for alopecia: an update, looking to the future
- 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
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease