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Research 31–60 of 94
- Nouvelles thérapeutiques dans la prise en charge de l’alopécie androgénétique
- Fibroblast heterogeneity and functions: insights from single-cell sequencing in wound healing, breast cancer, ovarian cancer and melanoma
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- TNC+ fibroblasts involve in skin inflammation via neuro-immune and interacting with T cells
- Two females with hair loss
- Hoxc13 polyglycine repeat gain-of-function drives mammalian integument evolution by altering targeted genes and interactions
- SPT6 maintains epidermal homeostasis by inhibiting an NF-κB-positive feedback loop to prevent excessive inflammation
- Alopezien und Hypotrichosen im Kindesalter
- Impaired metabolic effects of metformin in men with early-onset androgenic alopecia
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- A systematic simulation-based meta-analytical framework for prediction of physiological biomarkers in alopecia
- Expression of Signaling Components in Embryonic Eyelid Epithelium
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Genome-wide detection of RNA editing events during the hair follicles cycle of Tianzhu white yak
- Interaction of the AKT and β-catenin signalling pathways and the influence of photobiomodulation on cellular signalling proteins in diabetic wound healing
- Fibroblasts: Origins, definitions, and functions in health and disease
- Spatial and Single-Cell Transcriptional Profiling Identifies Functionally Distinct Human Dermal Fibroblast Subpopulations
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- SHISA6 Confers Resistance to Differentiation-Promoting Wnt/β-Catenin Signaling in Mouse Spermatogenic Stem Cells
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family
- The developmental basis of fingerprint pattern formation and variation
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Single-Cell RNA Profiling of Human Skin Reveals Age-Related Loss of Dermal Sheath Cells and Their Contribution to a Juvenile Phenotype
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Transcriptome Reveals Long Non-coding RNAs and mRNAs Involved in Primary Wool Follicle Induction in Carpet Sheep Fetal Skin
- CXCL12+ dermal fibroblasts promote neutrophil recruitment and host defense by recognition of IL-17
- Gata6 promotes hair follicle progenitor cell renewal by genome maintenance during proliferation
- Genetic Hair Disorders: A Review