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Research 30 of 107
- Molecular Genetics of Alopecias
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- Genetics of Alopecia
- Biology and Genetics of Hair
- Isolated autosomal recessive woolly hair/hypotrichosis: genetics, pathogenesis and therapies
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- An Autosomal Recessive Woolly Hair/Hypotrichosis Case with LIPH Mutation in a Turkish Patient
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Inherited Disorders of the Hair
- Keratin 71 Mutations: From Water Dogs to Woolly Hair
- Identification and Characterization of a Novel Lysophosphatidic Acid Receptor, p2y5/LPA6
- Identification of 736T>A mutation of lipase H in Japanese siblings with autosomal recessive woolly hair
- 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
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Genetics of Structural Hair Disorders
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Computational derivation of a molecular framework for hair follicle biology from disease genes
- Discovery of genes and proteins possibly regulating mean wool fibre diameter using cDNA microarray and proteomic approaches
- Transcriptome sequencing reveals the key genes associated with hair follicle development in Qianhua Mutton Merino
- Identification of potential key genes and pathways associated with the Pashmina fiber initiation using RNA-Seq and integrated bioinformatics analysis
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Molecular mechanism of ligand recognition and activation of lysophosphatidic acid receptor LPAR6
- Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient
- Non-Edg family LPA receptors: the cutting edge of LPA research
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- 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
- Novel small‐insertion mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis