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Research 31–60 of 120
- Resequencing Analyses Revealed Genetic Diversity and Selection Signatures during Rabbit Breeding and Improvement
- Genetics of Alopecia
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Autosomal recessive woolly hair/hypotrichosis with homozygous mutation in the <i>LIPH</i> gene: a case report
- Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient
- Molecular Basis of Hereditary Hair Diseases
- 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
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- White piedra caused by <i>Trichosporon inkin</i> : a report of two cases in a northern climate
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Trichoscopy in Hair Shaft Disorders
- The eyelash follicle features and anomalies: A review
- Fibroproliferative genes are preferentially expressed in central centrifugal cicatricial alopecia
- Hair Loss in Children
- Group IID, IIE, IIF and III secreted phospholipase A2s
- Mutations in Sterol O-Acyltransferase 1 (Soat1) Result in Hair Interior Defects in AKR/J Mice
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Advances in Hair Diseases
- Aberrant inflammasome activation as a driving force of human autoimmune skin disease
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Integrating multi-omics analyses of Nonomuraea dietziae to reveal the role of soybean oil in [(4′-OH)MeLeu]4-CsA overproduction
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- 192 MicroRNAs and their regulatory interactions in the human hair follicle
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- LPA-producing enzyme PA-PLA<sub>1</sub>α regulates hair follicle development by modulating EGFR signalling
- The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis