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Research 661–690 of 1000+
- The anti‐apoptotic Bcl‐2 protein regulates hair follicle stem cell function
- Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome
- From structural resilience to cell specification — Intermediate filaments as regulators of cell fate
- A Concise Review of Organoid Tissue Engineering: Regenerative Applications and Precision Medicine
- Comprehensive Analysis of LncRNA AC010789.1 Delays Androgenic Alopecia Progression by Targeting MicroRNA-21 and the Wnt/β-Catenin Signaling Pathway in Hair Follicle Stem Cells
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Screening of circRNAs Associated with Secondary Wool Follicle Development in Fine-Wool Sheep and Construction of Their ceRNA Network
- Recent Advances in the Role of Fibroblast Growth Factors in Hair Follicle Growth
- Emerging biomedical engineering strategies for hair follicle regeneration
- Functional regeneration strategies of hair follicles: advances and challenges
- Unlocking the genetic secrets of Dorper sheep: insights into wool shedding and hair follicle development
- Prioritizing susceptibility genes for the prognosis of male-pattern baldness with transcriptome-wide association study
- Epidermal–dermal coupled spheroids are important for tissue pattern regeneration in reconstituted skin explant cultures
- M-CSF-stimulated myeloid cells can convert into epithelial cells to participate in re-epithelialization and hair follicle regeneration during dermal wound healing
- Stimulation of ectodermal organ development by Ectodysplasin-A1
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Early inductive events in ectodermal appendage morphogenesis
- Identification of dkk4 as a target of Eda-A1/Edar pathway reveals an unexpected role of ectodysplasin as inhibitor of Wnt signalling in ectodermal placodes
- Uncombable hair syndrome: Observations on response to biotin and occurrence in siblings with ectodermal dysplasia
- The Wnt inhibitor, Dickkopf 4, is induced by canonical Wnt signaling during ectodermal appendage morphogenesis
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- Ectoderm-Targeted Overexpression of the Glucocorticoid Receptor Induces Hypohidrotic Ectodermal Dysplasia
- Ectodermal Dysplasia: Otolaryngologic Manifestations and Management
- Salivary gland function in persons with ectodermal dysplasias
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Alopecia in congenital hidrotic ectodermal dysplasia responding to treatment with a combination of topical minoxidil and tretinoin
- FGF-9 accelerates epithelial invagination for ectodermal organogenesis in real time bioengineered organ manipulation
- Loss of a homologous group of proteins in a dominantly inherited ectodermal malformation