المؤلفون: Elsadig Mohamed Ahmed, Mohamed E. Elangeeb, Khalid Mohamed Adam, Hytham Ahmed Abuagla, Abubakr Ali Elamin MohamedAhmed, Elshazali Widaa Ali, Elmoiz Idris Eltieb, Ali M. Edris, Hiba Mahgoub Ali Osman, Ebtehal Saleh Idris, Khalil A. A. Khalil

المصدر: Journal of Personalized Medicine, Vol 14, Iss 4, p 425 (2024)

مصطلحات موضوعية: non-synonymous single nucleotide polymorphisms, insulin genes, permanent neonatal diabetes mellitus, genetic variations, computational methods, personalized medicine, Medicine

وصف الملف: electronic resource

العلاقة: https://www.mdpi.com/2075-4426/14/4/425Test; https://doaj.org/toc/2075-4426Test

الوصول الحر: https://doaj.org/article/cdba5c2914ed4e6289f223716b3a7c56Test

المؤلفون: Mohamed E. Elnageeb, Imadeldin Elfaki, Khalid M. Adam, Elsadig Mohamed Ahmed, Elkhalifa M. Elkhalifa, Hytham A. Abuagla, Abubakr Ali Elamin Mohamed Ahmed, Elshazali Widaa Ali, Elmoiz Idris Eltieb, Ali M. Edris

المصدر: Diseases, Vol 11, Iss 3, p 115 (2023)

مصطلحات موضوعية: synucleinopathies, Parkinson’s disease (PD), alpha-synuclein (α-Syn) protein, SNCA gene non-synonymous single nucleotide polymorphisms (nsSNPs), bioinformatics, Medicine

وصف الملف: electronic resource

العلاقة: https://www.mdpi.com/2079-9721/11/3/115Test; https://doaj.org/toc/2079-9721Test

الوصول الحر: https://doaj.org/article/7e4efb7a3b474742a149683a58dd6c02Test

المؤلفون: Khyber Shinwari, Hafiz Muzzammel Rehman, Guojun Liu, Mikhail A. Bolkov, Irina A. Tuzankina, Valery. A. Chereshnev

المصدر: Frontiers in Molecular Biosciences, Vol 9 (2022)

مصطلحات موضوعية: TCIRG1 gene mutation, congenital neutropenia, osteopetrosis, non-synonymous single nucleotide polymorphisms, molecular dynamics simulation (MD), Biology (General), QH301-705.5

وصف الملف: electronic resource

العلاقة: https://www.frontiersin.org/articles/10.3389/fmolb.2022.879875/fullTest; https://doaj.org/toc/2296-889XTest

الوصول الحر: https://doaj.org/article/dbb4b16282644205bd9611afe387bf79Test

المؤلفون: Shinwari, K., Rehman, H. M., Liu, G., Bolkov, M. A., Tuzankina, I. A., Chereshnev, V. A.

المصدر: Frontiers in Molecular Biosciences

مصطلحات موضوعية: CONGENITAL NEUTROPENIA, MOLECULAR DYNAMICS SIMULATION (MD), NON-SYNONYMOUS SINGLE NUCLEOTIDE POLYMORPHISMS, OSTEOPETROSIS, TCIRG1 GENE MUTATION

وصف الملف: application/pdf

العلاقة: 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 / K. Shinwari, H. M. Rehman, G. Liu et al. // Frontiers in Molecular Biosciences. — 2022. — Vol. 9. — 879875.; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85130154514&doi=10.3389%2ffmolb.2022.879875&partnerID=40&md5=f2a96fd1444d5dad9dcc0c579438f930Test; http://elar.urfu.ru/handle/10995/117884Test; 85130154514; 000795675700001

الإتاحة: https://doi.org/10.3389/fmolb.2022.879875Test
http://elar.urfu.ru/handle/10995/117884Test

المؤلفون: Tanushree Tunstall, Jody Phelan, Charlotte Eccleston, Taane G. Clark, Nicholas Furnham

المصدر: Frontiers in Molecular Biosciences, Vol 8 (2021)

مصطلحات موضوعية: Mycobacterium tuberculosis, pncA, nsSNPs, non-synonymous Single Nucleotide Polymorphisms, biophysical effects, thermodynamic stability, Biology (General), QH301-705.5

وصف الملف: electronic resource

العلاقة: https://www.frontiersin.org/articles/10.3389/fmolb.2021.619403/fullTest; https://doaj.org/toc/2296-889XTest

الوصول الحر: https://doaj.org/article/f14da148a8894aba827cd6d6942720aeTest

المؤلفون: Dae-Jin Kwon, Yeong-Sup Lee, Donghyun Shin, Kyeong-Hye Won, Ki-Duk Song

المصدر: Asian-Australasian Journal of Animal Sciences, Vol 32, Iss 2, Pp 290-296 (2019)

مصطلحات موضوعية: Yucatan Miniature Pigs, Functional Annotation, Next Generation Sequencing, Non-synonymous Single Nucleotide Polymorphisms, Genetic Association Database, Animal culture, SF1-1100, Animal biochemistry, QP501-801

وصف الملف: electronic resource

العلاقة: http://www.ajas.info/upload/pdf/ajas-18-0170.pdfTest; https://doaj.org/toc/1011-2367Test; https://doaj.org/toc/1976-5517Test

الوصول الحر: https://doaj.org/article/3c46ead20f7f48ad839b4a4caa332359Test

المؤلفون: Donghyun Shin, Jae-Don Oh, Kyeong-Hye Won, Ki-Duk Song

المصدر: Asian-Australasian Journal of Animal Sciences, Vol 31, Iss 8, Pp 1150-1159 (2018)

مصطلحات موضوعية: Berkshire, Functional Annotation, Next Generation Sequencing, Non-synonymous Single Nucleotide Polymorphisms, Selective Sweep, Animal culture, SF1-1100, Animal biochemistry, QP501-801

وصف الملف: electronic resource

العلاقة: http://www.ajas.info/upload/pdf/ajas-31-8-1150.pdfTest; https://doaj.org/toc/1011-2367Test; https://doaj.org/toc/1976-5517Test

الوصول الحر: https://doaj.org/article/b629fd40c11d477c913320d5c1a17a5aTest

المؤلفون: Khyber Shinwari, Hafiz Muzzammel Rehman, Guojun Liu, Mikhail A. Bolkov, Irina A. Tuzankina, Valery. A. Chereshnev

مصطلحات موضوعية: Biochemistry, Molecular Biology, Structural Biology, Enzymes, Protein Trafficking, Proteomics and Intermolecular Interactions (excl. Medical Proteomics), Receptors and Membrane Biology, Signal Transduction, Structural Biology (incl. Macromolecular Modelling), Synthetic Biology, TCIRG1 gene mutation, congenital neutropenia, osteopetrosis, non-synonymous single nucleotide polymorphisms, molecular dynamics simulation (MD)

العلاقة: https://figshare.com/articles/dataset/Table1_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_DOCX/19669818Test

الإتاحة: https://doi.org/10.3389/fmolb.2022.879875.s003Test
https://figshare.com/articles/dataset/Table1_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_DOCX/19669818Test

المؤلفون: Khyber Shinwari, Hafiz Muzzammel Rehman, Guojun Liu, Mikhail A. Bolkov, Irina A. Tuzankina, Valery. A. Chereshnev

مصطلحات موضوعية: Biochemistry, Molecular Biology, Structural Biology, Enzymes, Protein Trafficking, Proteomics and Intermolecular Interactions (excl. Medical Proteomics), Receptors and Membrane Biology, Signal Transduction, Structural Biology (incl. Macromolecular Modelling), Synthetic Biology, TCIRG1 gene mutation, congenital neutropenia, osteopetrosis, non-synonymous single nucleotide polymorphisms, molecular dynamics simulation (MD)

العلاقة: https://figshare.com/articles/dataset/DataSheet1_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_CSV/19669812Test

الإتاحة: https://doi.org/10.3389/fmolb.2022.879875.s001Test
https://figshare.com/articles/dataset/DataSheet1_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_CSV/19669812Test

المؤلفون: Udhaya Kumar S, Ambritha Balasundaram, Hephzibah Cathryn R, Rinku Polachirakkal Varghese, Siva R, Gnanasambandan R, Salma Younes, Hatem Zayed, George Priya Doss C

المصدر: Computers in Biology and Medicine. 148:105701

مصطلحات موضوعية: Male, Lung Neoplasms, PPI network, Precision medicine, Pathway enrichment analysis, Forkhead Transcription Factors, Pathogenic variants, Health Informatics, Polymorphism, Single Nucleotide, Computer Science Applications, Repressor Proteins, Phosphatidylinositol 3-Kinases, Non-small cell lung cancer, Carcinoma, Non-Small-Cell Lung, Whole-exome sequencing, Exome Sequencing, Non-synonymous single nucleotide polymorphisms, Humans

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3254fabd3e7c40ebeb86ccf0455c8998Test
https://doi.org/10.1016/j.compbiomed.2022.105701Test