scholarly journals Structure and function analyses of the purified GPCR human vomeronasal type 1 receptor 1

2011 ◽  
Vol 1 (1) ◽  
Author(s):  
Karolina Corin ◽  
Philipp Baaske ◽  
Sandra Geissler ◽  
Christoph J. Wienken ◽  
Stefan Duhr ◽  
...  
2018 ◽  
Vol 87 (2) ◽  
pp. 136-145 ◽  
Author(s):  
Shana V. Stoddard ◽  
Colin L. Welsh ◽  
Maggie M. Palopoli ◽  
Serena D. Stoddard ◽  
Mounika P. Aramandla ◽  
...  

2018 ◽  
Vol 23 (2) ◽  
pp. 115-121
Author(s):  
Xavier Lieben Louis ◽  
Pema Raj ◽  
Kathleen J. McClinton ◽  
Liping Yu ◽  
Miyoung Suh ◽  
...  

2016 ◽  
Vol 26 (2) ◽  
pp. 218-226 ◽  
Author(s):  
Yang Yu ◽  
Igor D. Petrik ◽  
Kelly N. Chacón ◽  
Parisa Hosseinzadeh ◽  
Honghui Chen ◽  
...  

2021 ◽  
Vol 45 (7) ◽  
pp. S7
Author(s):  
Evan Lewis ◽  
Leif Erik Lovblom ◽  
Sebastien Lanctot ◽  
Daniel Scarr ◽  
Vera Bril ◽  
...  

2019 ◽  
Author(s):  
Tebyan A. Abdelhameed ◽  
Mohamed Mustafa Osman Fadul ◽  
Dina Nasereldin Abdelrahman Mohamed ◽  
Amal Mohamed Mudawi ◽  
Sayaf Kamal Khalifa Fadul Allah ◽  
...  

ABSTRACTBackgroundGenetic polymorphisms in the HEXA gene are associated with a neurodegenerative disorder called Tay-Sachs disease (TSD) (GM2 gangliosidosis type 1). This study aimed to predict the possible pathogenic SNPs of this gene and their impact on the protein using different bioinformatics tools.MethodsSNPs retrieved from the NCBI database were analyzed using several bioinformatics tools. The different algorithms collectively predicted the effect of single nucleotide substitution on both structure and function of the hexosaminidase A protein.ResultsFifty nine mutations were found to be highly damaging to the structure and function of the HEXA gene protein.ConclusionAccording to this study, thirty two novel nsSNP in HEXA are predicted to have possible role in Tay-Saches Disease using different bioinformatics tools. Our findings could help in genetic study and diagnosis of Tay-Saches Disease.


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