Search
for
Sort by
Research 211–240 of 1000+
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Rapid Genetic Analysis of Epithelial-Mesenchymal Signaling During Hair Regeneration
- Potential genetic associations of acne scar phenotypes: IL1A in fibrotic scarring and CYB5R1 in atrophic scarring
- Biology and Genetics of Hair
- Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies
- Dermatopathology and molecular genetics
- Female patients complaining about hair loss: documentation of defective scalp hair dynamics with contrast-enhanced phototrichogram
- Analysis of genetic polymorphisms of steroid 5α-reductase type 1 and 2 genes in Korean men with androgenetic alopecia
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit)
- Development of polycystic ovary syndrome: involvement of genetic and environmental factors
- Deciphering the cellular landscape and genetic underpinnings of fiber diameter determined by dermal papilla cells in fine-wool sheep
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Targeted elimination of the follicular label-retaining cells by photo-induced cell killing caused a defect on follicular renewal on mice
- Pluripotent Stem Cell Technology: A Promising Remedy for Hypopigmentation Disorders
- Tissue regenerative delays and synthetic lethality in adult mice after combined deletion of Atr and Trp53
- BMP-FGF Signaling Axis Mediates Wnt-Induced Epidermal Stratification in Developing Mammalian Skin
- Cicatricial (Scarring) Alopecias
- Genetic hair and nail disorders
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Defining the identity of mouse embryonic dermal fibroblasts
- Getting to grips with hair loss
- Tissue Retinol‐Binding Protein 4 Expression and Its Genetic Variants (rs3758539) in Patients With Severe and Treatment‐Refractory Alopecia Areata: Association With Response to Baricitinib
- Development of a mouse model for Hutchinson-Gilford progeria syndrome reveal defects in adult stem cell maintenance
- THE PATHOGENESIS OF ALOPECIA AREATA
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- 244 Defective maintenance of hair follicle stem cells through COL17A1 loss orchestrates the hair follicle aging program
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study
- Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation