Cargando…

A new parameter in multiple myeloma: CYP3A4*1B single nucleotide polymorphism

Multiple myeloma (MM) is a disease caused by malignant plasma cells, causing free light chain release accompanying the increase in monoclonal immunoglobulin. Cytochrome P450 (CYP) is one of the large and functional enzyme families composed of various hemoproteins. This protein network has been shown...

Descripción completa

Detalles Bibliográficos
Autores principales:	Serin, Istemi, Pehlivan, Sacide, Gundes, Ilknur, Fidan Oyaci, Yasemin, Pehlivan, Mustafa
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Springer Berlin Heidelberg 2020
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7653211/ https://www.ncbi.nlm.nih.gov/pubmed/33170343 http://dx.doi.org/10.1007/s00277-020-04339-1

Ejemplares similares

What are the roles of global DNA and APC 2 gene promotor hypermethylation in multiple myeloma?
por: Pehlivan, Sacide, et al.
Publicado: (2021)

Epigenetic and genetic investigation of SOCS-1 gene in patients with multiple myeloma
por: Tuncel, Fatıma Ceren, et al.
Publicado: (2022)

PB2075: HOW EFFECTIVE ARE LEPTIN GENE POLYMORPHISMS AND METHYLATION DURING THE COURSE OF MULTIPLE MYELOMA (MM)?
por: Serin, Istemi, et al.
Publicado: (2023)

The miRNA 196a2 rs11614913 variant has prognostic impact on Turkish patients with multiple myeloma
por: Kirik, Melya Pelin, et al.
Publicado: (2020)

Effect of the uncoupling protein-2 (UCP-2) and nuclear receptor subfamily 3 group C member 1 (NR3C1) genes on treatment efficacy and survival in patients with multiple myeloma: a single-center study
por: Demir, Ilknur, et al.
Publicado: (2021)

Medication-related osteonecrosis of the jaw (MRONJ) and eNOS Polymorphisms in multiple myeloma patients: a single center experience
por: Taş Ozyurtseven, Betul, et al.
Publicado: (2021)

Association of intron 4 VNTR polymorphism in the NOS3 gene with rapid cycling and treatment resistance in bipolar disorder: a case-control study
por: Aytac, Hasan M., et al.
Publicado: (2022)

PB1967: ROLE OF CYTOKINES IN MULTIPLE MYELOMA: IL-1RN AND IL-4 VNTR POLYMORPHISMS
por: Serin, I., et al.
Publicado: (2022)

COMTVal158Met polymorphism is associated with ecstasy (MDMA)-induced psychotic symptoms in the Turkish population
por: Aytac, Hasan Mervan, et al.
Publicado: (2022)

DNA Methylation Pattern of Gene Promoters of MB-COMT, DRD2, and NR3C1 in Turkish Patients Diagnosed with Schizophrenia
por: Aytac, Hasan Mervan, et al.
Publicado: (2022)

A New Clock is Running for Multiple Myeloma: Circadian Clock Protein-Period 3 (PER-3) Polymorphism
por: Serin, I., et al.
Publicado: (2023)

Mannose-Binding Lectin 2 Gene Polymorphism during Pandemic: COVID-19 Family
por: Tukek, Tufan, et al.
Publicado: (2022)

Investigation of MBL2 and NOS3 functional gene variants in suspected COVID-19 PCR (–) patients
por: Pehlivan, Sacide, et al.
Publicado: (2021)

PB1968: EPIGENETIC AND GENETIC INVESTIGATION OF SOCS-1 GENE IN PATIENTS WITH MULTIPLE MYELOMA
por: Serin, I., et al.
Publicado: (2022)

DNA Repair Genes and Chronic Myeloid Leukemia: ERCC2 (751), XRCC1 (399), XRCC4-Intron 3, XRCC4 (-1394) Gene Polymorphisms
por: Ozdilli, Kursat, et al.
Publicado: (2021)

Quantitative detection of methylated SOCS-1 in schizophrenia and bipolar disorder considering SOCS-1 -1478 CA/del polymorphism and clinical parameters
por: Aytac, H.M., et al.
Publicado: (2022)

Evaluation of Cardiac Parameters in Bone Marrow Transplant Patients: Effect of Pulmonary Artery Pressure on Survival
por: Özdöver, Ali Caner, et al.
Publicado: (2019)

Is There a Link between Circadian Clock Protein PERIOD 3 (PER3) (rs57875989) Variant and the Severity of COVID-19 Infection?
por: Yesil Sayin, Gozde, et al.
Publicado: (2021)

Investigation of inflammation related gene polymorphism of the mannose-binding lectin 2 in schizophrenia and bipolar disorder
por: Aytac, Hasan M., et al.
Publicado: (2021)

Genetic Variation of Myeloperoxidase Gene Contributes to Aggressive Periodontitis: A Preliminary Association Study in Turkish Population
por: Erciyas, Kamile, et al.
Publicado: (2010)

First Genetic Screening for Maternal Uniparental Disomy of Chromosome 7 in Turkish Silver-Russell Syndrome Patients
por: Karaca, Emin, et al.
Publicado: (2012)

DNA Repair Gene (XPD, XRCC4, and XRCC1) Polymorphisms in Patients with Endometrial Hyperplasia: A Pilot Study
por: Öztürk, Ebru, et al.
Publicado: (2018)

Mannose Binding Lectin and Macrophage Migration Inhibitory Factor Gene Polymorphisms in Turkish Children with Cardiomyopathy: No Association with MBL2 Codon 54 A/B Genotype, but an Association between MIF -173 CC Genotype
por: Col-Araz, Nilgun, et al.
Publicado: (2012)

Cytokine Gene Polymorphisms in Childhood Dilated Cardiomyopathy: Interferon- gamma, Tumor Necrosis Factor-alpha and Transforming Growth Factor - beta 1 Genes Are Associated with the Disease in Turkish Patients
por: Balci, Sibel Oguzkan, et al.
Publicado: (2013)

Association of the TNF-α, IL-2, and IL-2RB gene variants with susceptibility to psoriasis in a Turkish cohort
por: Gulel, Aslihan, et al.
Publicado: (2018)

Computational Analysis of Functional Single Nucleotide Polymorphisms Associated with the CYP11B2 Gene
por: Jia, Minyue, et al.
Publicado: (2014)

The Relationship Between Hematological Parameters and Mortality in Cardiovascular Patients With Postcardiac Arrest Syndrome
por: Erol, Mehmet K, et al.
Publicado: (2019)

Trends in the Frequency of HLA DR-DQ Haplotypes Among Children and Adolescents with Type 1 Diabetes Mellitus in the Southeast Region of Turkey
por: Keskin, Mehmet, et al.
Publicado: (2012)

The effect of Kefir consumption on blood pressure some blood parameters in hypertensive individuals: Erkan Pehlivan
por: Ozyazgan Tokay, A, et al.
Publicado: (2022)

Possible role of CYP2C9 & CYP2C19 single nucleotide polymorphisms in drug refractory epilepsy
por: Lakhan, Ram, et al.
Publicado: (2011)

Effects of the SLCO1B1 A388G single nucleotide polymorphism on the development, clinical parameters, treatment, and survival of multiple myeloma cases in a Polish population
por: Michalska, Katarzyna, et al.
Publicado: (2022)

No influence of the polymorphisms CYP2C19 and CYP2D6 on the efficacy of cyclophosphamide, thalidomide, and bortezomib in patients with Multiple Myeloma
por: Vangsted, Annette J, et al.
Publicado: (2010)

Effect of shearing on some physiological and hormonal parameters in Akkaraman sheep
por: Pehlivan, Erkan, et al.
Publicado: (2020)

The use of bevacizumab in primary malignant tumors of the central nervous system: A single-center experience
por: Pehlivan, Metin, et al.
Publicado: (2023)

SUN-711 Association of Single Nucleotide Polymorphisms of CYP11B2, CYP11B1 and CYP17A1 with Primary Aldosteronism in a Multi-Ethnic Malaysian Cohort
por: Azam, Afifah, et al.
Publicado: (2020)

Association of Single Nucleotide Polymorphisms in CYP1B1 and COMT Genes with Breast Cancer Susceptibility in Indian Women
por: Yadav, Sharawan, et al.
Publicado: (2009)

A single nucleotide polymorphism in CYP1B1 leads to differential prostate cancer risk and telomere length
por: Gu, Cheng-Yuan, et al.
Publicado: (2018)

Estimation of CYP3A4*1B single nucleotide polymorphism in patients with recurrent Major Depressive Disorder
por: Świechowski, Rafał, et al.
Publicado: (2019)

Prevalence of malnutrition in COPD and its relationship with the parameters related to disease severity
por: Mete, Burak, et al.
Publicado: (2018)

Individualized treatment based on CYP3A5 single-nucleotide polymorphisms with tacrolimus in ulcerative colitis
por: Okabayashi, Shinji, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_2i57b1aa4o9pt6gga6qhaa3muu