Buchumschlag

Development of ARMS PCR tests for detection of common CFTR gene mutations

Aim. To develop diagnostic assays, based on the amplification refractory mutation system (ARMS) principle, for detection of common mutations in the CFTR gene using two approaches: standard PCR with further gel-electrophoresis and Real-Time PCR with SYBR Green. Materials. For this study we have chose...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Вiopolymers and Cell
Datum:	2010
Hauptverfasser:	Soloviov, O.O., Pampukha, V.M., Livshits, L.A.
Format:	Artikel
Sprache:	Englisch
Veröffentlicht:	Інститут молекулярної біології і генетики НАН України 2010
Schlagworte:	Biomedicine
Online Zugang:	https://nasplib.isofts.kiev.ua/handle/123456789/154183
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!
Назва журналу:	Digital Library of Periodicals of National Academy of Sciences of Ukraine
Zitieren:	Development of ARMS PCR tests for detection of common CFTR gene mutations / O.O. Soloviov, V.M. Pampukha, L.A. Livshits // Вiopolymers and Cell. — 2010. — Т. 26, № 5. — С. 378-383. — Бібліогр.: 12 назв. — англ.

Institution

Digital Library of Periodicals of National Academy of Sciences of Ukraine

Ähnliche Einträge

Study on occurrence of the IVS8-5T allele of the CFTR gene in Ukrainian males with spermatogenesis failure
von: Fesai, O.A., et al.
Veröffentlicht: (2010)

Novel gene PUS3 c.A212G mutation in Ukrainian family with intellectual disability
von: Gulkovskyi, R.V., et al.
Veröffentlicht: (2015)

Detection of V617F mutation of gene jak2 at patients with chronic myeloproliferative neoplasms
von: Dybkov, M.V., et al.
Veröffentlicht: (2010)

Analysis of mutations in GBA gene in Ukrainian patients with Gaucher disease
von: Olkhovych, N.V., et al.
Veröffentlicht: (2017)

Association of genetic polymorphism with the mutation status of the BRCA1/2 genes in spontanous breast cancer
von: Polinyk, S.I., et al.
Veröffentlicht: (2017)

Familial adenomatous polyposis: age of onset and association with mutations of the APC gene in patients from West Ukraine
von: Lozynska, M.R., et al.
Veröffentlicht: (2017)

Association of the EPHA1 gene polymorphism with idiopathic mild intellectual disability
von: Gulkovskyi, R.V., et al.
Veröffentlicht: (2015)

Association of the leukemia inhibitory factor gene polymorphism rs929271 with idiopathic mild intellectual disability
von: Gulkovskyi, R.V., et al.
Veröffentlicht: (2015)

Molecular-genetic characterization of Ukrainian patients with mucopolysaccharidosis I: identification of three new mutations in α-L-iduronidase gene
von: Trofimova, N.S., et al.
Veröffentlicht: (2016)

Molecular-genetic characterization of Ukrainian patients with mucopolysaccharidosis IIIA: identification of three new mutations in the heparan-N-sulfatase gene
von: Trofimova, N.S., et al.
Veröffentlicht: (2016)

Identification and characterization of six new mutations in GLB1 gene in Ukrainian patients with GM1 gangliosidosis and Morquio B disease
von: Mytsyk, N.Y., et al.
Veröffentlicht: (2016)

EPHA1 gene SNPs analysis in population of Ukraine
von: Gulkovskyi, R.V., et al.
Veröffentlicht: (2013)

Spectrum of mutations in patients with organic acidurias from Ukraine
von: Barvinska, O.I., et al.
Veröffentlicht: (2018)

The role of IL6 and ESR1 gene polymorphisms as immunological factors of pregnancy maintenance
von: Kucherenko, A.M., et al.
Veröffentlicht: (2013)

Association of IL8 and IL10 gene allelic variants with ischemic stroke risk and prognosis
von: Kucherenko, A.M., et al.
Veröffentlicht: (2014)

Study of SNRPN genetic and epigenetic mutations in Prader-Willi and Angelman patients
von: Chernushyn, S.Yu., et al.
Veröffentlicht: (2018)

Single center study of ESBL-related strains of Enterobacteriaceae collected from clinical specimens of infants with the congenital heart disease using multiplex PCR amplification
von: Filonenko, G.V., et al.
Veröffentlicht: (2017)

Ischemic stroke in Ukrainian population: possible involvement of the F2 G20210A, F5 G1691A and MTHFR C677T gene variants
von: Tatarskyy, P.F., et al.
Veröffentlicht: (2010)

New techniques for mutation analysis in some exons of PAH and CFTR gene of men using denaturing gradient gel-electrophoresis
von: O. O. Soloviov, et al.
Veröffentlicht: (2008)

Study on possible role of CYP1A1, GSTT1, GSTM1, GSTP1, NAT2 and ADRB2 genes polymorphisms in bronchial asthma development in children
von: Tatarskyy, P.F., et al.
Veröffentlicht: (2011)

13q Deletions detected by fluorescence in situ hybridization for diagnosis and prognosis of chronic lymphoproliferative neoplasms
von: Sitko, V.V., et al.
Veröffentlicht: (2015)

Expression patterns of genes that regulate lipid metabolism in prostate tumors
von: Gerashchenko, G.V., et al.
Veröffentlicht: (2018)

Contribution of chromosomal abnormalities and genes of the major histocompatibility complex to early pregnancy losses
von: Tkach, I.R., et al.
Veröffentlicht: (2015)

Suppression of tumorigenicity and metastatic potential of melanoma cells by transduction of interferon gene
von: Lykhova, A.A., et al.
Veröffentlicht: (2014)

Association of allelic polymorphisms of the Matrix Gla-protein system genes with acute coronary syndrome in the Ukrainian population
von: Garbuzova, V.Yu., et al.
Veröffentlicht: (2015)

The polymorphisms of genes involved in DNA methylation in patients with malignancies from West Ukraine
von: Dmytruk, I.M., et al.
Veröffentlicht: (2016)

The peculiarities of gene expression of medullary breast carcinoma tumor-associated antigens in different types of breast tumors
von: Shyian, А., et al.
Veröffentlicht: (2012)

Association of genotypes by polymorphic variant C-108T of PON1 gene with the risk of developing breast cancer and hypertensive disease in women
von: Fishchuk, L.Ye.
Veröffentlicht: (2014)

PPM1M and PRICKLE2 are potential tumor suppressor genes in human clear-cell renal cell carcinoma
von: Rudenko, E.E., et al.
Veröffentlicht: (2014)

T-138C polymorphism of MGP gene is associated with blood plasma cholesterol levels but not related to other risk factors of atherosclerosis in patients with ischemic stroke
von: Garbuzova, V.Yu., et al.
Veröffentlicht: (2014)

Genetic variants in the PSMA6, PSMC6 and PSMA3 genes associated with childhood asthma in Latvian and Taiwanese populations
von: Paramonova, N., et al.
Veröffentlicht: (2014)

Study of association between polymorphisms in the PSMB5 (rs11543947) and PSMA3 (rs2348071) genes and multiple sclerosis in Latvians
von: Kalnina, J., et al.
Veröffentlicht: (2014)

Study on association of the polymorphic variants of ACE (I/D), AT2R1 (A1166C), TNF-a (G308A), MTHFR (C677T) genes and their combinations with the risk of development of perinatal pathology and gestation reduction
von: Gorovenko, N.G., et al.
Veröffentlicht: (2011)

Comparative analysis of epigenetic markers in plasma and tissue of patients with colorectal cancer
von: Kondratov, A.G., et al.
Veröffentlicht: (2014)

Autoantibodies against tyrosyl-tRNA synthetase and its separated domains at essential hypertension
von: Grom, M.Yu., et al.
Veröffentlicht: (2015)

Implementation of the quantitative Real-Time PCR for the molecular-genetic diagnostics of spinal muscular atrophy
von: Soloviov, O.O., et al.
Veröffentlicht: (2010)

Glutathione transferase activity and reduce glutathione content in the cytosol of rat gastric mucosa cells under carcinogen N-methyl-N'-nitro-Nnitrosoguanidine treatment
von: M.O. TymoshenkО, M.O. TymoshenkО, O.O. Kravchenko, L.M. Gaida, O.V. Lynchak, N.I. Ruzhytska, L.I. Ostapchenko O.O. Kravchenko, L.M. Gaida, O.V. Lynchak, N.I. Ruzhytska, L.I. Ostapchenko
Veröffentlicht: (2012)

Expression of ITSN2 and TKS5 in different subtypes of breast cancer tumors
von: Kropyvko, S.V., et al.
Veröffentlicht: (2019)

Aberrant expression of metallothioneins in clear cell renal cell carcinomas
von: Rymar, V.I., et al.
Veröffentlicht: (2015)

Effect of anticancer drugs on breast cancer cells sensitive and resistant to doxorubicin: expression of mRNAs of TGF-β and its receptors
von: Chorna, I.V., et al.
Veröffentlicht: (2014)