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Research 61–90 of 99
- Current Genetics in Hair Diseases
- Monilethrix, a rare inherited hair shaft disorder in siblings
- Transglutaminase-3 Enzyme: A Putative Actor in Human Hair Shaft Scaffolding?
- The development of an in vitro human hair follicle organoid with a complexity similar to that in vivo
- Hair and Nail Relationship
- Genetics of Wool and Cashmere Fibre: Progress, Challenges, and Future Research
- A Novel Type II Cytokeratin, mK6irs, is Expressed in the Huxley and Henle Layers of the Mouse Inner Root Sheath
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Monilethrix Treated with Minoxidil
- Woolly Antics between the Sheaths
- Hair shaft disorders
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- <i>Hoxc13</i> mutant mice lack external hair
- Advances in Hair Diseases
- Dermatoscopy of hair shaft disorders
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Clinical relevance of hair microscopy in alopecia
- Disorders of hair in children
- Towards a molecular understanding of hair loss and its treatment
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Light microscopy of the hair: A simple tool to "untangle" hair disorders
- Hair Loss in Children
- A study of phenotypic correlation with the genotypic status of HTM regions of KRTHB6 and KRTHB1 genes in monilethrix families of Indian origin
- Hox in hair growth and development
- Monilethrix – Case report of a rare disease
- Monilethrix: A rare hereditary condition
- Case Report: 7 Year-Old Saudi Female with Monilethrix
- Wanted, dead and alive: Why a multidisciplinary approach is needed to unlock hair treatment potential
- Molecular Genetics of Human Hair Diseases
- A review of genotrichoses and hair pathology associated with inherited skin diseases