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Research 91–120 of 1000+
- Regulatory pathways implicated in male androgenetic alopecia pathogenesis
- A new mutation resulting in the truncation of the TRAF6-interacting domain of XEDAR: a possible novel cause of hypohidrotic ectodermal dysplasia: Figure 1
- Inflammation in androgenetic alopecia and hair loss: linking neurosciences-endocrinology-dermatology
- Genomic Markers and Personalized Medicine in Androgenetic Alopecia: A Comprehensive Review
- Siberian cats help in solving part of the mystery surrounding golden cats
- Vitiligo and alopecia areata: apples and oranges?
- Melanocytes: The new Black
- Does Complement Have a Role in the Pathogenesis of Alopecia Areata?
- Inherited Disorders of the Hair
- Identification of Key Pathways and Genes Related to the Development of Hair Follicle Cycle in Cashmere Goats
- Genome-Wide Association Study of Alopecia Areata in Taiwan: The Conflict Between Individuals and Hair Follicles
- Transcriptomic crossroads: Decoding genes and pathways that connect alopecia areata with chronic inflammatory skin disorders
- A single-cell transcriptomic atlas elucidates the hair cycle and apoptosis mechanisms in goat hair follicles
- The polygenic architecture of hidradenitis suppurativa reveals signaling mechanisms that implicate epithelial remodeling
- Molecular mechanisms underlying cashmere quality differences between Jiangnan cashmere goats and Changthangi pashmina goats
- Association study reveals a susceptibility locus with male pattern baldness in the Han Chinese population
- Frontal fibrosing alopecia: An update on the hypothesis of pathogenesis and treatment
- Integrated miRNA-mRNA analysis reveals regulatory pathways underlying the curly fleece trait in Chinese tan sheep
- Insights into Male Androgenetic Alopecia: Differential Gene Expression Profiling of Plucked Hair Follicles and Integration with Genetic Data
- Androgenetic alopecia
- Nonclassic congenital adrenal hyperplasia
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- Human epidermal neural crest stem cells as a source of Schwann cells
- Susan Lee Lindquist (1949–2016)—pioneer in the study of cellular protein folding and disease
- Healthy individuals genetically at-risk for the development of Pemphigus vulgaris or Alopecia areata share disease-like cytokine dysregulation
- Molecular Mechanisms and Targeted Therapeutics in Androgenetic Alopecia: From Signaling Pathways to Regenerative Approaches
- Altered hair root gene expression profiles highlight calcium signaling and lipid metabolism pathways to be associated with curly hair initiation and maintenance in Mangalitza pigs
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Faculty Opinions recommendation of Hidradenitis suppurativa as a potential subtype of autoinflammatory keratinization disease.
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation