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Research 31–60 of 436
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- m6A Methylation Analysis Reveals Networks and Key Genes Underlying the Coarse and Fine Wool Traits in a Full-sib Merino Family
- Combined drug triads for synergic neuroprotection in retinal degeneration
- Inherited Disorders of the Hair
- A Comprehensive Review of GWASs of Human Hair Traits
- The Transcriptional Regulator Prdm1 Is Essential for the Early Development of the Sensory Whisker Follicle and Is Linked to the Beta-Catenin First Dermal Signal
- Global Landscapes of Human Phenotypic Variation in Inherited Traits
- Current Genetics in Hair Diseases
- Advances in the genetic understanding of hypohidrotic ectodermal dysplasia
- Facial skin aging: an integrative analysis of genetics, epigenetics, and lifestyle factors
- Genetics of Alopecia
- Divergent genetic mechanism leads to spiny hair in rodents
- Dumhetens rum i bildningens mitt
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS
- Research Snippets
- Repurposing of Various Current Medicines as Radioprotective Agents
- Cosmeceutical Treatments for Androgenetic Alopecia
- Feather arrays are patterned by interacting signalling and cell density waves
- Epidermal patterning and induction of different hair types during mouse embryonic development
- Anatomy and Physiology of Hair
- Lgr5 Stem Cells and Potential Treatments for Hair Loss
- Biology and Genetics of Hair
- sQuiz your knowledge: Polycyclic annular plaques on the trunk following dutasteride treatment
- The biology and genetics of curly hair
- Minoxidil suppressed mitochondrial depolarization and subsequent neuronal cell death by decreasing intracellular potassium level
- Bone morphogenetic protein signaling drives rete ridge morphogenesis: a distinct epidermal appendage program
- Análise da qualidade de vida em indivíduos com alopecia pós-COVID-19
- Significant Correction of Disease after Postnatal Administration of Recombinant Ectodysplasin A in Canine X-Linked Ectodermal Dysplasia
- Molecular basis of hypohidrotic ectodermal dysplasia: an update