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Research 31–60 of 117
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Genetic Hair Disorders: A Review
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- Novel small‐insertion mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis
- Genetics of Alopecia
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- Botanical extracts in combination improve autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations
- Clinicopathological insights into the phenotypic variation of autosomal recessive hypotrichosis/wooly hair by c.736T>A LIPH mutation
- Unexpectedly high carrier rates and genotype/phenotype correlation; LIPH mutations in Japanese autosomal recessive woolly hair/hypotrichosis
- 197 A novel splice site mutation in LIPH identified in a Japanese patient with autosomal recessive woolly hair
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Biology and Genetics of Hair
- Congenital hair loss disorders: Rare, but not too rare
- Identification of factors contributing to phenotypic divergence via quantitative image analyses of autosomal recessive woolly hair/hypotrichosis with homozygous c.736T>A<i>LIPH</i>mutation
- Prevalent founder mutation c.736T>A of <i>LIPH</i> in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood
- Isolated autosomal recessive woolly hair/hypotrichosis: genetics, pathogenesis and therapies
- Molecular Genetics of Alopecias
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Topical minoxidil improves congenital hypotrichosis caused by <i>LIPH</i> mutations
- Identification of 736T>A mutation of lipase H in Japanese siblings with autosomal recessive woolly hair
- Inherited Disorders of the Hair
- Homozygous missense mutation in the<i>LIPH</i>gene causing autosomal recessive hypotrichosis simplex in a Chinese patient
- Current Genetics in Hair Diseases
- Distinct genotype-phenotype patterns in non-syndromic hereditary hypotrichosis: a multicenter Chinese cohort
- Resequencing Analyses Revealed Genetic Diversity and Selection Signatures during Rabbit Breeding and Improvement