نتائج البحث

1

Relationship between TP53 and interleukin-6 gene variants and the risk of types 1 and 2 diabetes mellitus development in the Kermanshah province

المؤلفون: Ramin Sabzi, Lida Haghnazari

المصدر: Journal of Medicine and Life

مصطلحات موضوعية: Adult, Blood Glucose, Male, medicine.medical_specialty, type 2 diabetes mellitus, Population, Single-nucleotide polymorphism, Biology, Iran, Polymorphism, Single Nucleotide, Body Mass Index, Young Adult, Insulin resistance, Gene Frequency, Polymorphism (computer science), Risk Factors, single nucleotide polymorphism, Internal medicine, Genotype, medicine, SNP, Humans, Genetic Predisposition to Disease, TP53, Allele, education, Glycated Hemoglobin, education.field_of_study, Interleukin-6, Type 2 Diabetes Mellitus, General Medicine, Middle Aged, medicine.disease, Endocrinology, Diabetes Mellitus, Type 1, Diabetes Mellitus, Type 2, Case-Control Studies, Female, Original Article, Tumor Suppressor Protein p53, type 1 diabetes mellitus

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::940e6b5db3d8681fb7bfa3faef5aee06Test
https://pubmed.ncbi.nlm.nih.gov/33767783Test

2

Investigation of the relationship between MMP-1 (- 1607 1G/2G), MMP-3 (- 1171 5A/6A) gene variations and development of bladder cancer

المؤلفون: Arzu Ay, Nevra Alkanli, Gökhan Çevik

المصدر: Molecular biology reports. 48(12)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a5642e5d840d9a0d6a4255c9ea1c547Test
https://pubmed.ncbi.nlm.nih.gov/34693500Test

3

The rs11755527 polymorphism in the BACH2 gene and type 1 diabetes mellitus: case control study in a Brazilian population

المؤلفون: Cristine Dieter, Natália Emerim Lemos, Luiza Emy Dorfman, Guilherme Coutinho Kullmann Duarte, Taís Silveira Assmann, Daisy Crispim

المصدر: Archives of Endocrinology and Metabolism, Volume: 64, Issue: 2, Pages: 138-143, Published: 27 MAR 2020
Archives of Endocrinology and Metabolism, Vol 64, Iss 2, Pp 138-143 (2020)
Archives of Endocrinology and Metabolism v.64 n.2 2020
Arquivos de Endocrinologia e Metabolismo
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM

مصطلحات موضوعية: Adult, Male, Genotype, endocrine system diseases, Endocrinology, Diabetes and Metabolism, Population, Type 1 diabetes mellitus, 030209 endocrinology & metabolism, Single-nucleotide polymorphism, Polymerase Chain Reaction, Polymorphism, Single Nucleotide, Diseases of the endocrine glands. Clinical endocrinology, BACH2 gene, 03 medical and health sciences, 0302 clinical medicine, Gene Frequency, Risk Factors, medicine, Humans, SNP, Genetic Predisposition to Disease, education, Allele frequency, Genetics, Type 1 diabetes, education.field_of_study, business.industry, Case-control study, DNA polymorphisms, Middle Aged, RC648-665, medicine.disease, Minor allele frequency, Basic-Leucine Zipper Transcription Factors, Diabetes Mellitus, Type 1, Case-Control Studies, 030220 oncology & carcinogenesis, Medicine, Female, business, Brazil

وصف الملف: text/html

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5fc8cd13ff8301d7791bcdaccca727dTest
https://doi.org/10.20945/2359-3997000000214Test

4

Genetic polymorphisms in DNA repair genes XRCC1 and 3 are associated with increased risk of breast cancer in Bangladeshi population

المؤلفون: Amir Hossain, Razia Sultana, Syed Mozammel Hossain, Nupur Rani Howlader, Mostafizur Rahman, Abdul Mazid, Mustafizur Rahman

المصدر: Breast cancer research and treatment. 182(3)

مصطلحات موضوعية: 0301 basic medicine, Adult, Cancer Research, medicine.medical_specialty, Adolescent, DNA Repair, Genotype, Population, Single-nucleotide polymorphism, Breast Neoplasms, Gastroenterology, Polymorphism, Single Nucleotide, 03 medical and health sciences, XRCC1, Young Adult, 0302 clinical medicine, Breast cancer, XRCC3, Risk Factors, Internal medicine, Biomarkers, Tumor, Medicine, Humans, Genetic Predisposition to Disease, Allele, education, Aged, education.field_of_study, Bangladesh, business.industry, Middle Aged, medicine.disease, Prognosis, Genotype frequency, DNA-Binding Proteins, 030104 developmental biology, X-ray Repair Cross Complementing Protein 1, Oncology, 030220 oncology & carcinogenesis, Case-Control Studies, Female, business, Follow-Up Studies

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a7690930140c27be6d22e4a33382499Test
https://pubmed.ncbi.nlm.nih.gov/32562117Test

5

Association of interleukin 1 receptor antagonist (IL1RN) gene polymorphism with recurrent pregnancy loss risk in the North Indian Population and a meta-analysis

المؤلفون: Rohini R. Nair, Kiran Singh, Anuradha Khanna

المصدر: Molecular Biology Reports. 41:5719-5727

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3369cdf57d2653107b0dc774899cacdTest
https://doi.org/10.1007/s11033-014-3443-8Test

6

Association of CYP2E1, STK15 and XRCC1 Polymorphisms with Risk of Breast Cancer in Malaysian Women

المؤلفون: Eric Tzyy Jiann Chong, Kek Heng Chua, Ping Chin Lee, Lucky Poh Wah Goh, Jitt Aun Chuah, Edwin Un Hean See

المصدر: Asian Pacific Journal of Cancer Prevention. 17:647-653

مصطلحات موضوعية: 0301 basic medicine, Oncology, Cancer Research, Epidemiology, Bioinformatics, Polymerase Chain Reaction, XRCC1, Breast cancer screening, 0302 clinical medicine, Risk Factors, Genotype, Aurora Kinase A, education.field_of_study, medicine.diagnostic_test, Cytochrome P-450 CYP2E1, Prognosis, DNA-Binding Proteins, Lymphatic Metastasis, 030220 oncology & carcinogenesis, Female, Polymorphism, Restriction Fragment Length, Adult, medicine.medical_specialty, Population, Breast Neoplasms, Single-nucleotide polymorphism, Polymorphism, Single Nucleotide, 03 medical and health sciences, Breast cancer, Internal medicine, parasitic diseases, Biomarkers, Tumor, medicine, Humans, SNP, Genetic Predisposition to Disease, Neoplasm Invasiveness, Allele, education, Neoplasm Staging, business.industry, Malaysia, Public Health, Environmental and Occupational Health, medicine.disease, X-ray Repair Cross Complementing Protein 1, 030104 developmental biology, Case-Control Studies, business, Follow-Up Studies

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4e3c43479ccb9a66214a425e2b68b9bTest
https://doi.org/10.7314/apjcp.2016.17.2.647Test

7

Association between the c.*229C>T polymorphism of the topoisomerase IIβ binding protein 1 (TopBP1) gene and breast cancer

المؤلفون: Agnieszka Szymczyk, Waldemar Różański, Beata Smolarz, Paweł Jóźwiak, Magdalena Bryś, Ewa Brzeziańska, Hanna Romanowicz-Makowska, Grażyna Chwatko, Anna Krześlak, Ewa Forma

المساهمون: E. Forma A. Krześlak P. Jóźwiak A. Szymczyk M. Bryś Department of Cytobiochemistry, University of Łodz, Pomorska 141/143, 90-236 Lodz, Poland, E. Brzeziańska Department of Molecular Bases of Medicine, Medical University of Łodz, Pomorska 251, 92-213 Lodz, Poland, G. Chwatko Department of Environmental Chemistry, University of Łodz, Pomorska 163, 90-236 Lodz, Poland, B. Smolarz H. Romanowicz-Makowska Department of Clinical Pathomorphology, Polish Mother’s Memorial Hospital Research Institute, Łodz, Rzgowska 281/289, 93-338 Lodz, Poland, W. Różański 2nd Department of Urology, Medical University of Łodz, Pabianicka 62, 93-513 Lodz, Poland

المصدر: Molecular Biology Reports

مصطلحات موضوعية: Adult, Genotype, Population, Single-nucleotide polymorphism, Breast Neoplasms, Biology, Polymorphism, Single Nucleotide, Article, Breast cancer, Gene Frequency, Risk Factors, Genetics, medicine, Odds Ratio, Humans, Genetic Predisposition to Disease, Genetic variation, Allele, Polymorphism, education, Molecular Biology, Allele frequency, 3' Untranslated Regions, Alleles, Aged, Neoplasm Staging, Aged, 80 and over, education.field_of_study, Base Sequence, Nuclear Proteins, General Medicine, Middle Aged, TOPBP1 Gene, medicine.disease, Topoisomerase IIβ binding protein 1, Minor allele frequency, DNA-Binding Proteins, Topoisomerase IIb binding protein 1, Case-Control Studies, Cancer research, Female, Neoplasm Grading, Carrier Proteins

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d10c55a3063c534f80cdaa9b524f1b6bTest
http://europepmc.org/articles/PMC3611025Test

8

Polymorphisms in DNA Repair Genes (APEX1, XPD, XRCC1 and XRCC3) and Risk of Preeclampsia in a Mexican Mestizo Population

المؤلفون: Fernando Vazquez-Alaniz, José M. Salas-Pacheco, Marisela Aguilar-Durán, Osmel La Llave-León, Francisco X. Castellanos-Juárez, Alfredo Téllez-Valencia, Marcelo Barraza-Salas, Ada Agustina Sandoval-Carrillo, Edna M. Méndez-Hernández

المصدر: International Journal of Molecular Sciences; Volume 15; Issue 3; Pages: 4273-4283
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 15, Iss 3, Pp 4273-4283 (2014)

مصطلحات موضوعية: Oncology, APEX1, XRCC1, DNA Repair, Severity of Illness Index, lcsh:Chemistry, Gene Frequency, Pre-Eclampsia, XRCC3, Pregnancy, Risk Factors, Genotype, DNA-(Apurinic or Apyrimidinic Site) Lyase, Odds Ratio, lcsh:QH301-705.5, Spectroscopy, Genetics, education.field_of_study, General Medicine, Computer Science Applications, DNA-Binding Proteins, Female, Adult, medicine.medical_specialty, Adolescent, XPD, Population, Biology, Polymorphism, Single Nucleotide, Article, Catalysis, preeclampsia, Inorganic Chemistry, Young Adult, Internal medicine, medicine, Humans, Genetic Predisposition to Disease, Physical and Theoretical Chemistry, education, Mexico, Molecular Biology, Allele frequency, Xeroderma Pigmentosum Group D Protein, polymorphisms, Chi-Square Distribution, Organic Chemistry, Case-control study, Odds ratio, Logistic Models, X-ray Repair Cross Complementing Protein 1, lcsh:Biology (General), lcsh:QD1-999, Case-Control Studies

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b2e3922f89695b4ad9bf127085f0bb8Test
https://doi.org/10.3390/ijms15034273Test

9

Interaction of XRCC1 and XPD Gene Polymorphisms with Lifestyle and Environmental Factors Regarding Susceptibility to Lung Cancer in a High Incidence Population in North East India

المؤلفون: Jagadish Mahanta, Rup Kumar Phukan, Gaganpreet Singh Sekhon, Santanu Kumar Sharma, Bhaskar Jyoti Saikia

المصدر: Asian Pacific Journal of Cancer Prevention. 15:1993-1999

مصطلحات موضوعية: Adult, Male, Oncology, Cancer Research, medicine.medical_specialty, Lung Neoplasms, Genotype, Epidemiology, Population, India, Environment, Young Adult, Asian People, Risk Factors, Internal medicine, medicine, Humans, Genetic Predisposition to Disease, education, Lung cancer, Life Style, Aged, Xeroderma Pigmentosum Group D Protein, Aged, 80 and over, Genetics, education.field_of_study, Polymorphism, Genetic, business.industry, Incidence, Incidence (epidemiology), Confounding, Public Health, Environmental and Occupational Health, Odds ratio, Middle Aged, medicine.disease, Confidence interval, DNA-Binding Proteins, X-ray Repair Cross Complementing Protein 1, Case-Control Studies, Population study, Female, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bef31c46b18ea38187f0e8762a515726Test
https://doi.org/10.7314/apjcp.2014.15.5.1993Test

10

p53 codon 72 Pro homozygosity increases the risk of cutaneous melanoma in individuals with dark skin complexion and among noncarriers of melanocortin 1 receptor red hair variants

المؤلفون: Andreas Katsambas, Dorothea Polydorou, Helen Gogas, E. Kanavakis, V. Nikolaou, O. Papadopoulos, Gerasimos Dimisianos, Ch. Antoniou, D. Tsoutsos, P. Panagiotou, Alexandros Stratigos, I. Stefanaki

المصدر: British Journal of Dermatology. 156:357-362

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c41c9f9fa262996640c9cc630d2d419aTest
https://doi.org/10.1111/j.1365-2133.2006.07645.xTest

تنقيح النتائج