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Research 61–90 of 116
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- Autosomal recessive woolly hair/hypotrichosis with homozygous mutation in the <i>LIPH</i> gene: a case report
- Case of autosomal recessive woolly hair/hypotrichosis with compound heterozygous mutations in the <i>LIPH</i> gene at c.742C > A and c.614A > G: The first Japanese case
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- White piedra caused by <i>Trichosporon inkin</i> : a report of two cases in a northern climate
- Monilethrix: A case report imaged by trichoscopy, reflectance confocal microscopy and histopathology
- Dermatoscopy of hair shaft disorders
- Non-Edg family LPA receptors: the cutting edge of LPA research
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- LPA3, a unique G protein-coupled receptor for lysophosphatidic acid
- Mutations in Sterol O-Acyltransferase 1 (Soat1) Result in Hair Interior Defects in AKR/J Mice
- Genetics of Structural Hair Disorders
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Advances in Hair Diseases
- Diagnostic challenges in determining alopecia areata
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Congenital Atrichia: A Case Report
- 196 The endocannabinoid tone regulates human sebocyte biology
- 194 An underlying mechanism of hair loss in acrodermatitis enteropathica
- 192 MicroRNAs and their regulatory interactions in the human hair follicle
- Peer Review #2 of "Human hair shaft proteomic profiling: individual differences, site specificity and cuticle analysis (v0.1)"
- LPA-producing enzyme PA-PLA<sub>1</sub>α regulates hair follicle development by modulating EGFR signalling
- Marie‐Unna Hereditary Hypotrichosis or Autosomal Recessive Hereditary Hypotrichosis with Woolly Hair: The Diagnostic Dilemma of Labeling Cases with Hypotrichosis
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Alopezien und Hypotrichosen im Kindesalter
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.