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Research 30 of 94
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Molecular mechanism of ligand recognition and activation of lysophosphatidic acid receptor LPAR6
- Identification and Characterization of a Novel Lysophosphatidic Acid Receptor, p2y5/LPA6
- Autotaxin–lysophosphatidic acid– LPA <sub>3</sub> signaling at the embryo‐epithelial boundary controls decidualization pathways
- The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis
- Isolated autosomal recessive woolly hair/hypotrichosis: genetics, pathogenesis and therapies
- Molecular Genetics of Alopecias
- Inherited Disorders of the Hair
- Genetics of Alopecia
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- An Autosomal Recessive Woolly Hair/Hypotrichosis Case with LIPH Mutation in a Turkish Patient
- Non-Edg family LPA receptors: the cutting edge of LPA research
- Keratin 71 Mutations: From Water Dogs to Woolly Hair
- Biology and Genetics of Hair
- 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
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Identification of potential key genes and pathways associated with the Pashmina fiber initiation using RNA-Seq and integrated bioinformatics analysis
- Hair Loss in Children
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Computational derivation of a molecular framework for hair follicle biology from disease genes
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- LncRNAs regulate the cyclic growth and development of hair follicles in Dorper sheep
- 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
- Hair growth promoting effects of adipose tissue-derived stem cells
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient