نتائج البحث

1

Programmed cell death 1 (PDCD1) gene haplotypes and susceptibility of patients to basal cell carcinoma

المؤلفون: Effat Seyedhashemi, Hossein Motedayyen, Farshid Fathi, Ahmad Piroozmand, Reza ArefNezhad, Samaneh Mozafarpoor, Batool Zamani

المصدر: Molecular Biology Reports. 48:2047-2052

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de82f0febae58decb6f1e6b5fab5a3a2Test
https://doi.org/10.1007/s11033-020-06115-wTest

2

Polymorphisms in the 3′-UTR of SCD5 gene are associated with hepatocellular carcinoma in Korean population

المؤلفون: Gyeong Im Yu, Dong Hoon Shin, Seon Hee Yang, Jae Seok Hwang, Kwang Ho Mun

المصدر: Molecular Biology Reports. 45:1705-1714

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, medicine.medical_specialty, Carcinoma, Hepatocellular, Genotype, MMP1, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Gastroenterology, 03 medical and health sciences, 0302 clinical medicine, Asian People, Gene Frequency, Risk Factors, Internal medicine, Republic of Korea, Genetics, medicine, Humans, Genetic Predisposition to Disease, 3' Untranslated Regions, Molecular Biology, Gene, Alleles, Aged, Liver Neoplasms, Promoter, General Medicine, Middle Aged, medicine.disease, Genotype frequency, Minor allele frequency, 030104 developmental biology, Case-Control Studies, 030220 oncology & carcinogenesis, Hepatocellular carcinoma, Matrix Metalloproteinase 1, Stearoyl-CoA Desaturase

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::915b1ca305ad62c1284bbcbfe4c9ce70Test
https://doi.org/10.1007/s11033-018-4313-6Test

3

Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands

المؤلفون: Cecelia W. Lo, Stephen Sanders, Sarah U. Morton, Irina R. Tikhonoa, Samir Zaidi, Elizabeth Goldmuntz, Hongjian Qi, Richard B. Kim, Jonathan R. Kaltman, Jonathan G. Seidman, Xue Zeng, Jason Homsy, George A. Porter, W. Scott Watkins, Deepak Srivastava, Weni Chang, Martin Tristani-Firouzi, Seema Mital, James R. Knight, Qiongshi Lu, Steven R. DePalma, John E. Deanfield, Christopher Castaldi, J. William Gaynor, Yufeng Shen, Bruce D. Gelb, Mark W. Russell, Richard P. Lifton, Alessandro Giardini, Kaya Bilguvar, Wendy K. Chung, Jane W. Newburger, H. Joseph Yost, Sheng Chih Jin, Mark Yandell, Martina Brueckner, Shrikant Mane, Robert D. Bjornson, Wei Chien Hung, Amy E. Roberts, Junhui Zhang, Christine E. Seidman, Michael C. Sierant, Hongyu Zhao, Shozeb Haider

المصدر: Nature genetics
Nature genetics, vol 49, iss 11

مصطلحات موضوعية: Heart Defects, Congenital, Risk, Adult, Male, 0301 basic medicine, Proband, Heterozygote, Heart disease, Gene Expression, Genome-wide association study, Biology, Medical and Health Sciences, Article, Growth Differentiation Factor 1, Congenital, 03 medical and health sciences, Genotype, Genetics, medicine, Humans, Genetic Predisposition to Disease, Exome, cardiovascular diseases, Autistic Disorder, Child, Exome sequencing, Heart Defects, Tetralogy of Fallot, Myosin Heavy Chains, Homozygote, Case-control study, High-Throughput Nucleotide Sequencing, Biological Sciences, Vascular Endothelial Growth Factor Receptor-3, medicine.disease, Pedigree, 3. Good health, Editorial, 030104 developmental biology, Case-Control Studies, Mutation, Female, Cardiac Myosins, Genome-Wide Association Study, Developmental Biology

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::901990cdfca7f6f14265588f9eac4db8Test
https://doi.org/10.1038/ng.3970Test

4

Association of TUSC1 and DPF3 gene polymorphisms with male infertility

المؤلفون: Kiyomi Matsumiya, Teruaki Iwamoto, Akira Tsujimura, Kiyoshi Komatsu, E. Koh, Jiro Kanaya, Mikio Namiki, Atsushi Tajima, Jiro Eguchi, Chise Hasegawa, Miki Yoshiike, Youichi Sato, Naoki Itoh, Aiko Yamauchi, Shiari Nozawa

المصدر: Journal of Assisted Reproduction and Genetics. 35:257-263

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Infertility, Linkage disequilibrium, Population, Immunoglobulins, Single-nucleotide polymorphism, Biology, urologic and male genital diseases, Polymorphism, Single Nucleotide, Male infertility, Andrology, Double plant homeodomain fingers, 03 medical and health sciences, Asian People, Gene Frequency, Tumor suppressor candidate 1, Genetics, medicine, Humans, SNP, Genetic Predisposition to Disease, Oligozoospermia, Family 3, education, Infertility, Male, Genetics (clinical), Azoospermia, Genetic association, education.field_of_study, Tumor Suppressor Proteins, Membrane Proteins, Obstetrics and Gynecology, Oligospermia, General Medicine, medicine.disease, Single nucleotide polymorphism, DNA-Binding Proteins, Logistic Models, 030104 developmental biology, Reproductive Medicine, Case-Control Studies, Transcription Factors, Developmental Biology

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29014a47189bb78c028b84d800ad475eTest
https://doi.org/10.1007/s10815-017-1052-xTest

5

An analysis of the polymorphisms of the GLUT1 gene in urothelial cell carcinomas of the bladder and its correlation with p53, Ki67 and GLUT1 expressions

المؤلفون: C Xu, X Yang, Y Wang, N Ding, R Han, Y Sun

المصدر: Cancer Gene Therapy. 24:297-303

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Cancer Research, Genotype, Single-nucleotide polymorphism, Biology, medicine.disease_cause, Polymorphism, Single Nucleotide, HaeIII, 03 medical and health sciences, Gene Frequency, medicine, Humans, SNP, Genetic Predisposition to Disease, Allele, Molecular Biology, Alleles, Aged, Neoplasm Staging, Aged, 80 and over, Genetics, Glucose Transporter Type 1, Urethral Neoplasms, Carcinoma, Cancer, Middle Aged, bacterial infections and mycoses, medicine.disease, Immunohistochemistry, Molecular biology, Gene Expression Regulation, Neoplastic, Ki-67 Antigen, 030104 developmental biology, Case-Control Studies, biology.protein, bacteria, Molecular Medicine, Female, GLUT1, Neoplasm Grading, Tumor Suppressor Protein p53, Carcinogenesis, medicine.drug

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8261cdb046682b5d99e54c3011c8bfe1Test
https://doi.org/10.1038/cgt.2017.17Test

6

Gene–environment interactions between ERCC2, ERCC3, XRCC1 and cadmium exposure in nasal polyposis disease

المؤلفون: Rim Khlifi, Fernando Gil, Amel Hamza-Chaffai, Pablo Olmedo, Ahmed Rebai, Boutheina Hammami

المصدر: Journal of Applied Genetics. 58:221-229

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, medicine.medical_specialty, Tunisia, DNA Repair, Genotype, Disease, 010501 environmental sciences, Biology, Bioinformatics, 01 natural sciences, Gastroenterology, 03 medical and health sciences, XRCC1, Nasal Polyps, Risk Factors, Internal medicine, Genetics, medicine, Humans, Genetic Predisposition to Disease, Gene, Xeroderma Pigmentosum Group D Protein, 0105 earth and related environmental sciences, Polymorphism, Genetic, DNA Helicases, General Medicine, Odds ratio, Middle Aged, Confidence interval, DNA-Binding Proteins, X-ray Repair Cross Complementing Protein 1, 030104 developmental biology, Case-Control Studies, Etiology, ERCC2, Female, Gene-Environment Interaction, Cadmium

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ed0ac7eb7e19c3b436e1306865f2b7dTest
https://doi.org/10.1007/s13353-016-0375-0Test

7

Matrix metalloproteinase gene polymorphisms in chronic periodontitis: a case–control study in the Indian population

المؤلفون: Poulami Majumder, Subrata Kumar Dey, Sujay Ghosh

المصدر: Journal of Genetics. 98

مصطلحات موضوعية: Adult, Male, 0106 biological sciences, 0301 basic medicine, MMP3, Genotype, MMP1, Population, India, Biology, MMP8, Polymorphism, Single Nucleotide, 01 natural sciences, Young Adult, 03 medical and health sciences, Gene Frequency, Matrix Metalloproteinase 13, Genetics, Humans, Genetic Predisposition to Disease, Allele, Promoter Regions, Genetic, education, Genotyping, Alleles, Aged, education.field_of_study, Incidence, Case-control study, Middle Aged, Prognosis, Molecular biology, Matrix Metalloproteinases, Genotype frequency, Matrix Metalloproteinase 8, 030104 developmental biology, Case-Control Studies, Chronic Periodontitis, Female, Matrix Metalloproteinase 3, Matrix Metalloproteinase 1, Follow-Up Studies, 010606 plant biology & botany

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3c07135f1c1dd87677f86148beb372fTest
https://doi.org/10.1007/s12041-019-1077-2Test

8

Association of Uncoupling Protein 1 (UCP1) gene polymorphism with obesity: a case-control study

المؤلفون: Amein Al Ali, Zhara Al Ali, Sadananda Acharya, Chittibabu Vatte, Cyril Cyrus, Shahanas Chathoth, Khandaker Ahtesham Ahmed, Mona H Ismail, Aisha Mohammed Al Barqi

المصدر: BMC Medical Genetics
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-10 (2018)

مصطلحات موضوعية: Male, 0301 basic medicine, Gene Expression, Type 2 diabetes, Severity of Illness Index, Body Mass Index, Exon, 0302 clinical medicine, Gene Frequency, Polymorphism (computer science), Genotype, Uncoupling Protein 1, Genetics (clinical), education.field_of_study, Membrane Glycoproteins, Diabetes, Intracellular Signaling Peptides and Proteins, NCP1, Middle Aged, Cholesterol, Cohort, Female, Research Article, Adult, Risk, lcsh:Internal medicine, UCP1, medicine.medical_specialty, lcsh:QH426-470, HDL, Population, Saudi Arabia, 030209 endocrinology & metabolism, LDL, 03 medical and health sciences, Niemann-Pick C1 Protein, Internal medicine, Genetics, medicine, Humans, Genetic Predisposition to Disease, Obesity, lcsh:RC31-1245, education, Alleles, Triglycerides, Polymorphism, Genetic, Cholesterol, HDL, Case-control study, Moderate-obese, Extreme-obese, Cholesterol, LDL, Metabolic disorder, medicine.disease, lcsh:Genetics, 030104 developmental biology, Endocrinology, Diabetes Mellitus, Type 2, Case-Control Studies, Carrier Proteins

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80d6331c93f30486fefd131d94868635Test
https://doi.org/10.1186/s12881-018-0715-5Test

9

NRG1 variant effects in patients with Hirschsprung disease

المؤلفون: Raman Sethi, Alvin Santoso Kalim, Akhmad Makhmudi, Gunadi, Indra Adrianto, Lai Poh San, Nova Yuli Prasetyo Budi, Kristy Iskandar, Taufik Indrawan, Aditya Rifqi Fauzi

المصدر: BMC Pediatrics, Vol 18, Iss 1, Pp 1-9 (2018)
BMC Pediatrics

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Hirschsprung disease, Neuregulin-1, Population, Transcription factor binding motif, Polymerase Chain Reaction, Pathogenesis, 03 medical and health sciences, NRG1 variant, 0302 clinical medicine, Asian People, Polymorphism (computer science), medicine, Humans, Coding region, Genetic Predisposition to Disease, Neuregulin 1, education, Enhancer, Gene, Genetics, education.field_of_study, biology, business.industry, lcsh:RJ1-570, Genetic disorder, Genetic Variation, lcsh:Pediatrics, Sequence Analysis, DNA, medicine.disease, 030104 developmental biology, Indonesia, Case-Control Studies, 030220 oncology & carcinogenesis, Pediatrics, Perinatology and Child Health, biology.protein, Female, business, Research Article, Protein Binding, Transcription Factors

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07cc0a2fe045eb33924d002a0899cc87Test
https://doi.org/10.1186/s12887-018-1265-xTest

10

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

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