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Research 361–390 of 1000+
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Keratin intermediate filaments in the colon: guardians of epithelial homeostasis
- Top applications of dermatologic ultrasonography that can modify management
- Runx3 is involved in hair shape determination
- FOXN1 deficient nude severe combined immunodeficiency
- Black women’s hair: the main scalp dermatoses and aesthetic practices in women of African ethnicity
- EGFR Inhibitors and Cutaneous Complications: A Practical Approach to Management
- Keratinization of sheath and calamus cells in developing and regenerating feathers
- Bioengineering the Hair Follicle
- Autophagy-Mediated Cellular Remodeling during Terminal Differentiation of Keratinocytes in the Epidermis and Skin Appendages
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- Cutaneous manifestations of endocrine diseases in children
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- First Symposium of Ichthyosis Experts
- Cutaneous Adverse Events of Tyrosine Kinase Inhibitors in Endocrine Tumors: Clinical Features, Mechanisms, and Management Strategies
- Validity and Advantages of Three-Dimensional High-Frequency Ultrasound in Dermatological Evaluation
- 481 Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Organoids in skin wound healing
- Ectopic Expression of a Truncated Isoform of Hair Keratin 81 in Breast Cancer Alters Biophysical Characteristics to Promote Metastatic Propensity
- Convergent evolution has led to the loss of claw proteins in snakes and worm lizards
- Alopecia areata in a patient with WNT10A heterozygous ectodermal dysplasia
- Skin Manifestations of Rheumatological Diseases
- Pigmentary mosaicism: An update
- Dermatological care of gender‐diverse patients in Australia
- Trichotillomania
- Hair follicle-specific keratins and their diseases
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Type II Epithelial Keratin 6hf (K6hf) Is Expressed in the Companion Layer, Matrix, and Medulla in Anagen-Stage Hair Follicles