Associated Papers
Truncating PICK1 Variant Identified in Azoospermia Affected Mitochondrial Dysfunction in Knockout Mice.
Du YQ et al.
Current Medical Science, 2023
A Functional Variant Rs492554 Associated With Congenital Heart Defects Modulates SESN2 Expression Through POU2F1.
Yang W et al.
Frontiers in Cell and Developmental Biology, 2021
34249922 (PubMed )
Supplement: Table_1.xls › D1D2D3
Clinical Manifestations of Alport Syndrome-Diffuse Leiomyomatosis Patients With Contiguous Gene Deletions in COL4A6 and COL4A5.
Zhou X et al.
Frontiers in Medicine, 2021
34778325 (PubMed )
Supplement: Data_Sheet_2.PDF
ICA1L forms BAR-domain complexes with PICK1 and is crucial for acrosome formation in spermiogenesis.
He J et al.
Journal of Cell Science, 2015
Whole exome sequencing combined with integrated variant annotation prediction identifies asymptomatic Tangier disease with compound heterozygous mutations in ABCA1 gene.
Tada H et al.
Atherosclerosis, 2015
Association of mutations in the zona pellucida binding protein 1 (ZPBP1) gene with abnormal sperm head morphology in infertile men.
Yatsenko AN et al.
Molecular Human Reproduction, 2012
A newly discovered mutation in PICK1 in a human with globozoospermia.
Liu G et al.
Asian Journal of Andrology, 2010
Novel DPY19L2 variants in globozoospermic patients and the overcoming this male infertility.
Shang YL et al.
Asian Journal of Andrology, 0
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