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Research 961–990 of 1000+
- The Roles of WNT Signaling Pathways in Skin Development and Mechanical-Stretch-Induced Skin Regeneration
- Advances in Innovative Surgical Implant Manufacturing for Hernia Repair and Soft Tissue Reconstruction
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Innate type 2 immunity controls hair follicle commensalism by Demodex mites
- Molecular Conversations and the Development of the Hair Follicle and Basal Cell Carcinoma
- Basal cell carcinomas acquire secondary mutations to overcome dormancy and progress from microscopic to macroscopic disease
- Early embryonic exposure of freshwater gastropods to pharmaceutical 5-alpha-reductase inhibitors results in a surprising open-coiled “banana-shaped” shell
- Eflúvio telógeno após dermatite de contato no couro cabeludo
- Epidemiology and disease burden of androgenetic alopecia in college freshmen in China: A population-based study
- Diphenyl cresyl phosphate [MAK Value Documentations, 2003]
- Genetics of Diabetes in Childhood
- Pregestational overweight/obesity are associated with C-section and with LGA newborn in women attended in the public health system in Chile between 2015-2017*
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Trichotillomania in children and adolescents: Review of the literature and case report
- Folliculin interacts with p0071 (plakophilin-4) and deficiency is associated with disordered RhoA signalling, epithelial polarization and cytokinesis
- Control of hair follicle cell fate by underlying mesenchyme through a CSL–Wnt5a–FoxN1 regulatory axis
- APECED: JAK Inhibition in an Adult Case with Long-Term Follow-up
- Rapunzel syndrome: a rare form of trichobezoar in the stomach with some extension into the small intestine
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- Platelet Concentrates Preconditioning of Mesenchymal Stem Cells and Combined Therapies: Integrating Regenerative Strategies for Enhanced Clinical Applications
- Low level of maternal biotin intake changes the expression of biotin transporter in dams and fetuses in mice
- Potential Health Risks Associated with Cosmetics and Personal Care Products: An Overview
- <i>Hoxc13</i> mutant mice lack external hair
- 9 Role of 5α-reductase in health and disease
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Bioavailability of Albumin-Bound Testosterone†
- Development of polycystic ovary syndrome: involvement of genetic and environmental factors