Associated Papers
Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree.
Zhang X et al.
Frontiers in Genetics, 2025
Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis.
Xie Y et al.
Frontiers in Medicine, 2025
Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia.
Liquat N et al.
Archives of Dermatological Research, 2024
Cell-trafficking impairment in disease-associated LPA6 missense mutants and a potential pharmacoperone therapy for autosomal recessive woolly hair/hypotrichosis.
Yanagida K et al.
Human Molecular Genetics, 2023
Novel sequence variants in the LIPH and LPAR6 genes underlies autosomal recessive woolly hair/hypotrichosis in consanguineous families.
Ahmad F et al.
Congenital Anomalies, 2018
Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan.
Pedurupillay CR et al.
Genes, 2016
GESPA: classifying nsSNPs to predict disease association.
Khurana JK et al.
Bmc Bioinformatics, 2015
Genetic dissection of two Pakistani families with consanguineous localized autosomal recessive hypotrichosis (LAH).
Abbas S et al.
Iranian Journal of Basic Medical Sciences, 2014
In silico analysis of missense mutations in LPAR6 reveals abnormal phospholipid signaling pathway leading to hypotrichosis.
Raza SI et al.
Plos One, 2014
Mutations in LPAR6/P2RY5 and LIPH are associated with woolly hair and/or hypotrichosis.
Kurban M et al.
Journal of the European Academy of Dermatology and Venereology : Jeadv, 2013
Mutations in the LPAR6 and LIPH genes underlie autosomal recessive hypotrichosis/woolly hair in 17 consanguineous families from Pakistan.
Khan S et al.
Clinical and Experimental Dermatology, 2011
A novel mutation in LPAR6 causes autosomal recessive hypotrichosis of the scalp.
Nahum S et al.
Clinical and Experimental Dermatology, 2011
Novel mutations in the P2RY5 gene in one Turkish and two Indian patients presenting with hypotrichosis and woolly hair.
Pasternack SM et al.
Archives of Dermatological Research, 2009
Mutations in the P2RY5 gene underlie autosomal recessive hypotrichosis in 13 Pakistani families.
Tariq M et al.
The British Journal of Dermatology, 2009
Autosomal recessive woolly hair with hypotrichosis caused by a novel homozygous mutation in the P2RY5 gene.
Shimomura Y et al.
Experimental Dermatology, 2009
Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3).
Azeem Z et al.
Human Genetics, 2008
Disruption of P2RY5, an orphan G protein-coupled receptor, underlies autosomal recessive woolly hair.
Shimomura Y et al.
Nature Genetics, 2008