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Research 751–780 of 1000+
- Genetics of Inherited Ichthyoses and Related Diseases
- Examination of epigenetic inhibitor zebularine in treatment of skin wounds in healthy and diabetic mice
- 0977 Pathogenic hallmarks of primary lymphocyte-mediated scarring alopecia revealed by single nuclear and spatial multiomics
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Whiskers amiss, a new vibrissae and hair mutation near the Krt1 cluster on mouse Chromosome 11
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- KRT17: A Key Driver of Cancer Therapy Resistance and Emerging Therapeutic Target
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- KRT17 promotes endometrial cancer cell migration as well as angiogenesis by regulating HIF-1α/VEGF pathway
- KRT16 wt Allele
- Case of epidermolytic ichthyosis (bullous congenial ichthyosiform erythroderma) with a novel L157P mutation in KRT10 complicated by hypercalcemia
- Mice Expressing a Mutant Krt75 (K6hf) Allele Develop Hair and Nail Defects Resembling Pachyonychia Congenita
- Variation in the Exon 3–4 Region of Ovine KRT85 and Its Effect on Wool Traits
- Regenerative potential of CD200- subpopulations of hair follicle bulge
- Integration Analysis of Hair Follicle Transcriptome and Proteome Reveals the Mechanisms Regulating Wool Fiber Diameter in Angora Rabbits
- Activation of β-catenin signaling programs embryonic epidermis to hair follicle fate
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Expression patterns of keratin intermediate filament and keratin associated protein genes in wool follicles
- Keratins and disease at a glance
- Annotation of sheep keratin intermediate filament genes and their patterns of expression
- Keratin 17 in disease pathogenesis: from cancer to dermatoses
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- Comparative Anatomy of Mouse and Human Nail Units
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Hair greying is associated with active hair growth
- A Homozygous Frameshift Mutation in the<i>HOXC13</i>Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair