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Research 721–750 of 1000+
- Mendelian randomization study highlights hypothyroidism as a causal determinant of alopecia areata
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- Divergent progression pathways in male androgenetic alopecia and female pattern hair loss: Trichoscopic perspectives
- 83 Transcriptomic meta-analysis and deconvolution approaches unveil cellular dynamics in scarring and non-scarring primary lymphocytic alopecias
- Treatment modalities for lymphocytic and neutrophilic scarring alopecia
- Follicular dysplasia and hair loss in white-tailed deer (<i>Odocoileus virginianus</i>)
- Bioinformatic analysis of gene expression data reveals Src family protein tyrosine kinases as key players in androgenetic alopecia
- Cell Therapy for Androgenetic Alopecia: Elixir or Trick?
- Male pattern hair loss: Can developmental origins explain the pattern?
- 1438 KLF4 maintains hair follicle stem cell quiescence
- ORAL TOFACITINIB IN MODERATE AND SEVERE ALOPECIA AREATA: CASE SERIES OF 14 PATIENTS
- Decision letter: Live imaging reveals chromatin compaction transitions and dynamic transcriptional bursting during stem cell differentiation in vivo
- States and Fates of Skin Fibroblasts Revealed through Chromatin Accessibility
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- Bridging Personal and Population in Excitability Diseases: Will Studies of Rare Diseases Bring Generalizable Mechanisms From Monogenic Channelopathies?
- Alopecia areata mit gutem Ansprechen auf Tofacitinib
- Reliability of the Estimation of the Take of Split Thickness Graft by the Observation Method
- Utilizing functional genomics approaches to characterize risk genes in alopecia areata
- Hair Follicle Stem Cells and Hair Regeneration
- Spectrum of clinical manifestations of SLE patients from India and its correlation with KIR gene polymorphism
- Retinoids Modulate MITF: A Novel Mechanism in the Regulation of Melanogenesis
- Evolution in action: highlighting a role for the Agouti gene in development?
- Mysteries of salt and pepper
- Clinical Snippets
- 303 The role of rare variants in male-pattern hair loss: Analysis of whole exome sequencing data in the UK Biobank
- ESDR303 – The role of rare variants in male-pattern hair loss: Analysis of whole exome sequencing data in the UK Biobank
- Female Androgenetic (?) Alopecia
- The Rotterdam Study: objectives and design update
- Epidemiology, diagnosis, and management of polycystic ovary syndrome
- scMC learns biological variation through the alignment of multiple single-cell genomics datasets