Search
for
Sort by
Research 30 of 99
- Genetic mapping of hair loss through the APCDD1 gene pathway: A new perspective
- Biology and Genetics of Hair
- Genetics of Structural Hair Disorders
- Current Genetics in Hair Diseases
- A Synonymous Polymorphism of APCDD1 Affects Translation Efficacy and is Associated with Androgenic Alopecia
- Genetics of Alopecia
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Congenital hair loss disorders: Rare, but not too rare
- Editors' Picks
- News in brief
- A Synonymous Polymorphism of APCDD1 Affects Translation Efficacy and is Associated with Androgenic Alopecia
- Inherited Disorders of the Hair
- Distinct genotype-phenotype patterns in non-syndromic hereditary hypotrichosis: a multicenter Chinese cohort
- The Pathogenesis and Treatment Progress of Androgenic Alopecia
- Dynamic Signals for Hair Follicle Development and Regeneration
- Molecular Genetics of Alopecias
- Wasabi leaf extract changes the expression levels of cytokine related genes in dermal papilla cells, which identified by the whole transcriptome
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Hoxc13 polyglycine repeat gain-of-function drives mammalian integument evolution by altering targeted genes and interactions
- An Intrinsic Oscillation of Gene Networks Inside Hair Follicle Stem Cells: An Additional Layer That Can Modulate Hair Stem Cell Activities
- Human Fetal Scalp Dermal Papilla Enriched Genes and the Role of R-Spondin-1 in the Restoration of Hair Neogenesis in Adult Mouse Cells
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Comprehensive Transcriptome Profiling of Balding and Non-Balding Scalps in Trichorhinophalangeal Syndrome Type I Patient
- Precision therapeutics in non-scarring alopecia: a systemic genomic and pathway-based framework for targeted interventions
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- TNC+ fibroblasts involve in skin inflammation via neuro-immune and interacting with T cells