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Research 91–120 of 1000+
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- Delayed epidermal permeability barrier formation and hair follicle aberrations in Inv-Cldn6 mice
- The Cutaneous Epidermal Growth Factor Network: Can it be Translated Clinically to Stimulate Hair Growth?
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- White piedra caused by <i>Trichosporon inkin</i> : a report of two cases in a northern climate
- Medical and surgical therapies for alopecias in black women
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Matriptase Expression and Zymogen Activation in Human Pilosebaceous Unit
- DNA dioxygenases Tet2/3 regulate gene promoter accessibility and chromatin topology in lineage-specific loci to control epithelial differentiation
- Beyond Wavy Hairs
- Celsr1 and Celsr2 exhibit distinct adhesive interactions and contributions to planar cell polarity
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- PA05 A rare case of cardiocutaneous syndrome in a young child
- <i>WNT10A</i> , dermatology and dentistry
- Characterisation of the Ovine KRTAP36-1 Gene in Chinese Tan Lambs and Its Impact on Selected Wool Traits
- Comparative histomorphometric and transcriptomic analysis reveals potential genetic determinants of pelage variation between hairy and coarse-woolly sheep
- Defective trophoblast function in mice with a targeted mutation of Ets2
- m6A Methylation Analysis Reveals Networks and Key Genes Underlying the Coarse and Fine Wool Traits in a Full-sib Merino Family
- The spectrum of hair loss in patients with mycosis fungoides and Sézary syndrome
- dsRNA Released by Tissue Damage Activates TLR3 to Drive Skin Regeneration
- Ethnic Hair Disorders
- Congenital hair loss disorders: Rare, but not too rare
- Hair and scalp disorders in women of African descent: an overview
- Pathobiology of chemotherapy-induced hair loss
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Hair and Scalp Disorders in Women of African Descent
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders