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Research 91–120 of 1000+
- Platelet-rich plasma—an ‘Elixir’ for treatment of alopecia: personal experience on 117 patients with review of literature
- Hair shaft disorders in children – An update
- Small molecules facilitate single factor-mediated sweat gland cell reprogramming
- The Roles of EDA2R in Ageing and Disease
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- Ichthyosis with confetti: clinics, molecular genetics and management
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Mesenchymal Stem Cells for the Treatment of Skin Diseases
- AIRE Deficiency Leads to the Development of Alopecia Areata‒Like Lesions in Mice
- Current Genetics in Hair Diseases
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Generation and characterization of hair-bearing skin organoids from human pluripotent stem cells
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- The hair shaft: normality, abnormality, and genetics
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- Clinical Case Notes. Castleman's disease of the lacrimal gland
- Painful thickened skin on the soles of the feet
- Genetic hair and nail disorders
- Ruxolitinib Rescues Multiorgan Clinical Autoimmunity in Patients with APS-1
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- An Unusual Case of Diarrhea, Dysgeusia, and Grainy and Nodular Mucosa
- FOXN1 deficient nude severe combined immunodeficiency
- Skin Development and Disease: A Molecular Perspective
- From structural resilience to cell specification — Intermediate filaments as regulators of cell fate
- Phototherapy of androgenetic alopecia with low level narrow band 655-nm red light and 780-nm infrared light