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Research 31–60 of 920
- Keratins and disease at a glance
- 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
- A keratin 15 containing stem cell population from the hair follicle contributes to squamous papilloma development in the mouse
- Conversion of the Nipple to Hair-Bearing Epithelia by Lowering Bone Morphogenetic Protein Pathway Activity at the Dermal-Epidermal Interface
- Ichthyosis with confetti: clinics, molecular genetics and management
- Hair greying is associated with active hair growth
- Identification of the Key Genes Associated with Different Hair Types in the Inner Mongolia Cashmere Goat
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Generating mouse models of degenerative diseases using Cre/lox-mediated in vivo mosaic cell ablation
- Effect of Nutritional Restriction on the Hair Follicles Development and Skin Transcriptome of Chinese Merino Sheep
- p53 Is a Direct Transcriptional Repressor of Keratin 17: Lessons from a Rat Model of Radiation Dermatitis
- Dermatopathology and molecular genetics
- Extracellular proteoglycan decorin maintains human hair follicle stem cells
- Keratin 71 Mutations: From Water Dogs to Woolly Hair
- Semidominant Inheritance in Epidermolytic Ichthyosis
- The expression of equine keratins K42 and K124 is restricted to the hoof epidermal lamellae of Equus caballus
- The Human Type II Keratin Gene Cluster on Chromosome 12q13.13: Final Count or Hidden Secrets?
- Transgenic Immortalization of Human Dermal Fibroblasts Mediated Through the MicroRNA/SIRT1 Pathway
- A newborn presenting with congenital blistering
- Genome-wide identification, characterization, and expression analysis of keratin genes (KRTs) family in yak (Bos grunniens)
- 3D-SeboSkin Model for Human ex vivo Studies of Hidradenitis Suppurativa/Acne Inversa
- Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy
- Building Models for Keratin Disorders
- Establishment of a culture model for the prolonged maintenance of chicken feather follicles structure in vitro
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- Novel Quinazoline Derivative Induces Differentiation of Keratinocytes and Enhances Skin Barrier Functions against Th2 Cytokine-Mediated Signaling
- Transcriptome analysis reveals the genetic basis underlying the development of skin appendages and immunity in hedgehog (Atelerix albiventris)