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Novel Disease-Associated Missense Single-Nucleotide Polymorphisms Variants Predication by Algorithms Tools and Molecular Dynamics Simulation of Human TCIRG1 Gene Causing Congenital Neutropenia and Osteopetrosis. / Shinwari, Khyber; Rehman, Hafiz Muzzammel; Liu, Guojun et al.
In: Frontiers in Molecular Biosciences, Vol. 9, 879875, 28.04.2022.

Research output: Contribution to journal › Article › peer-review

Harvard

Shinwari, K, Rehman, HM, Liu, G, Bolkov, MA, Tuzankina, IA & Chereshnev, VA 2022, 'Novel Disease-Associated Missense Single-Nucleotide Polymorphisms Variants Predication by Algorithms Tools and Molecular Dynamics Simulation of Human TCIRG1 Gene Causing Congenital Neutropenia and Osteopetrosis', Frontiers in Molecular Biosciences, vol. 9, 879875. https://doi.org/10.3389/fmolb.2022.879875

APA

Shinwari, K., Rehman, H. M., Liu, G., Bolkov, M. A., Tuzankina, I. A., & Chereshnev, V. A. (2022). Novel Disease-Associated Missense Single-Nucleotide Polymorphisms Variants Predication by Algorithms Tools and Molecular Dynamics Simulation of Human TCIRG1 Gene Causing Congenital Neutropenia and Osteopetrosis. Frontiers in Molecular Biosciences, 9, [879875]. https://doi.org/10.3389/fmolb.2022.879875

Vancouver

Shinwari K, Rehman HM, Liu G, Bolkov MA, Tuzankina IA, Chereshnev VA. Novel Disease-Associated Missense Single-Nucleotide Polymorphisms Variants Predication by Algorithms Tools and Molecular Dynamics Simulation of Human TCIRG1 Gene Causing Congenital Neutropenia and Osteopetrosis. Frontiers in Molecular Biosciences. 2022 Apr 28;9:879875. doi: 10.3389/fmolb.2022.879875

Author

Shinwari, Khyber ; Rehman, Hafiz Muzzammel ; Liu, Guojun et al. / Novel Disease-Associated Missense Single-Nucleotide Polymorphisms Variants Predication by Algorithms Tools and Molecular Dynamics Simulation of Human TCIRG1 Gene Causing Congenital Neutropenia and Osteopetrosis. In: Frontiers in Molecular Biosciences. 2022 ; Vol. 9.

BibTeX

@article{40806d101d4743e6a7a04c1e15cfd5db,
title = "Novel Disease-Associated Missense Single-Nucleotide Polymorphisms Variants Predication by Algorithms Tools and Molecular Dynamics Simulation of Human TCIRG1 Gene Causing Congenital Neutropenia and Osteopetrosis",
keywords = "congenital neutropenia, molecular dynamics simulation (MD), non-synonymous single nucleotide polymorphisms, osteopetrosis, TCIRG1 gene mutation",
author = "Khyber Shinwari and Rehman, {Hafiz Muzzammel} and Guojun Liu and Bolkov, {Mikhail A.} and Tuzankina, {Irina A.} and Chereshnev, {Valery A.}",
note = "Publisher Copyright: Copyright {\textcopyright} 2022 Shinwari, Rehman, Liu, Bolkov, Tuzankina and Chereshnev.",
year = "2022",
month = apr,
day = "28",
doi = "10.3389/fmolb.2022.879875",
language = "English",
volume = "9",
journal = "Frontiers in Molecular Biosciences",
issn = "2296-889X",
publisher = "Frontiers Media S.A.",

}

RIS

TY - JOUR

T1 - Novel Disease-Associated Missense Single-Nucleotide Polymorphisms Variants Predication by Algorithms Tools and Molecular Dynamics Simulation of Human TCIRG1 Gene Causing Congenital Neutropenia and Osteopetrosis

AU - Shinwari, Khyber

AU - Rehman, Hafiz Muzzammel

AU - Liu, Guojun

AU - Bolkov, Mikhail A.

AU - Tuzankina, Irina A.

AU - Chereshnev, Valery A.

N1 - Publisher Copyright: Copyright © 2022 Shinwari, Rehman, Liu, Bolkov, Tuzankina and Chereshnev.

PY - 2022/4/28

Y1 - 2022/4/28

KW - congenital neutropenia

KW - molecular dynamics simulation (MD)

KW - non-synonymous single nucleotide polymorphisms

KW - osteopetrosis

KW - TCIRG1 gene mutation

UR - http://www.scopus.com/inward/record.url?scp=85130154514&partnerID=8YFLogxK

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=000795675700001

U2 - 10.3389/fmolb.2022.879875

DO - 10.3389/fmolb.2022.879875

M3 - Article

AN - SCOPUS:85130154514

VL - 9

JO - Frontiers in Molecular Biosciences

JF - Frontiers in Molecular Biosciences

SN - 2296-889X

M1 - 879875

ER -

ID: 30211182