نتائج البحث

1

Thrombin and plasmin generation in patients with plasminogen or plasminogen activator inhibitor type 1 deficiency

المؤلفون: Saskia E M Schols, Kathleen F. Betbadal, Sweta Gupta, Waander L. van Heerde, Joline L Saes, Amy D. Shapiro, Brandon M. Hardesty, Kitty Verbeek-Knobbe, Mark van Geffen

المصدر: Haemophilia, 25, 1073-1082
Haemophilia
Haemophilia, 25, 6, pp. 1073-1082

مصطلحات موضوعية: plasmin generation, Adult, Male, medicine.medical_specialty, Genotype, phenotype, Plasmin, medicine.medical_treatment, Vascular damage Radboud Institute for Health Sciences [Radboudumc 16], plasminogen deficiency, Coagulation Protein Disorders, 030204 cardiovascular system & hematology, Hemorrhagic Disorders, Thrombin generation, Fibrin, 03 medical and health sciences, 0302 clinical medicine, Thrombin, Internal medicine, Plasminogen Activator Inhibitor 1, Fibrinolysis, Humans, Medicine, Fibrinolysin, Child, Genetics (clinical), plasminogen activator inhibitor type 1 deficiency, biology, business.industry, Plasminogen Activator Inhibitor Type 1, Original Articles, Hematology, General Medicine, Middle Aged, Laboratory Science, Endocrinology, Coagulation, thrombin generation, Hemostasis, biology.protein, Original Article, Female, business, circulatory and respiratory physiology, 030215 immunology, medicine.drug

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a022a505ffebac999eebdffc9fb23825Test
https://doi.org/10.1111/hae.13842Test

2

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

3

Novel SNPs of WNK1 and AKR1C3 are associated with preeclampsia

المؤلفون: Cheng-Juan Sun, Wei-Yuan Zhang, Lin Li, Xue-Yan Li, Xiaowei Liu

المصدر: Gene. 668:27-32

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9eb03f51a8f51249a8d956bb329e381Test
https://doi.org/10.1016/j.gene.2018.05.055Test

4

A Polymorphism in the Gene Encoding the Insulin Receptor Binding Protein ENPP-1 Is Associated with Decreased Glomerular Filtration Rate in an Under-Investigated Indigenous African Population

المؤلفون: Eleanor Cave, Nigel J. Crowther, Jaya A. George, Katherine L. Prigge, Carolyn J. Padoa

المصدر: Kidney & Blood Pressure Research, Vol 45, Iss 6, Pp 1009-1017 (2020)

مصطلحات موضوعية: Adult, Male, lcsh:Diseases of the circulatory (Cardiovascular) system, medicine.medical_specialty, Black People, Renal function, rs1044498, lcsh:RC870-923, Polymorphism, Single Nucleotide, polymorphism, South Africa, Young Adult, Insulin resistance, Internal medicine, Diabetes mellitus, Genotype, lcsh:Dermatology, medicine, Humans, Pyrophosphatases, Allele, Aged, glomerular filtration rate, biology, Phosphoric Diester Hydrolases, business.industry, General Medicine, Middle Aged, lcsh:RL1-803, lcsh:Diseases of the genitourinary system. Urology, medicine.disease, Insulin receptor, Endocrinology, lcsh:RC666-701, Nephrology, Insulin receptor binding, biology.protein, Female, Kidney Diseases, Cardiology and Cardiovascular Medicine, business, ectonucleotide pyrophosphatase/phosphodiesterase 1, Kidney disease

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55f4f23ad1e1f8b314f2d78f85f05c10Test
https://doi.org/10.1159/000511213Test

5

Association between the -844 G>A, HindIII C>G, and 4G/5G PAI-1 Polymorphisms and Susceptibility to Multiple Sclerosis in Western Mexican Population

المؤلفون: José Francisco Muñoz-Valle, Xochil Trujillo, Miguel Ángel Macías-Islas, Baltazar-Rodríguez Luz Margarita, Miguel Huerta, Mario A. Mireles-Ramírez, Emmanuel Valdés-Alvarado, Jorge Gutierrez, Yeminia Valle

المصدر: Disease Markers, Vol 2019 (2019)
Disease Markers

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, medicine.medical_specialty, Multiple Sclerosis, Genotype, Article Subject, Plasmin, Clinical Biochemistry, Biology, HindIII, Polymerase Chain Reaction, Tissue plasminogen activator, 03 medical and health sciences, Sex Factors, 0302 clinical medicine, Internal medicine, Plasminogen Activator Inhibitor 1, Gene expression, Odds Ratio, Genetics, medicine, Humans, Genetic Predisposition to Disease, Allele, Mexico, Molecular Biology, Inflammation, lcsh:R5-920, Polymorphism, Genetic, Multiple sclerosis, Biochemistry (medical), General Medicine, Odds ratio, medicine.disease, 030104 developmental biology, Endocrinology, Tissue Plasminogen Activator, Disease Progression, biology.protein, Female, lcsh:Medicine (General), Polymorphism, Restriction Fragment Length, 030217 neurology & neurosurgery, Research Article, medicine.drug

وصف الملف: text/xhtml

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7df508d7cfc44d5101d8ad41981ceb55Test
https://doi.org/10.1155/2019/9626289Test

6

Vitamin D Pathway Genetic Variation and Type 1 Diabetes: A Case-Control Association Study

المؤلفون: Joana T Almeida, Manuel C. Lemos, Joana Guimarães, Dircea Rodrigues

المصدر: Genes
Genes, Vol 11, Iss 897, p 897 (2020)

مصطلحات موضوعية: Vitamin, Adult, Male, medicine.medical_specialty, Oxidoreductases Acting on CH-CH Group Donors, lcsh:QH426-470, Adolescent, type 1 diabetes, SNP, 030209 endocrinology & metabolism, Single-nucleotide polymorphism, 030204 cardiovascular system & hematology, Biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, single nucleotide polymorphism, Internal medicine, Genotype, Genetic variation, medicine, Vitamin D and neurology, Humans, genetics, Allele, Vitamin D, Child, Cytochrome P450 Family 2, Vitamin D3 24-Hydroxylase, Allele frequency, Genetics (clinical), Type 1 diabetes, Vitamin D-Binding Protein, Communication, autoimmune, medicine.disease, lcsh:Genetics, Endocrinology, Diabetes Mellitus, Type 1, chemistry, Cholestanetriol 26-Monooxygenase, Female

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d932899406db67727554f289903ce09bTest
https://pubmed.ncbi.nlm.nih.gov/32764491Test

7

Analysis of genetic polymorphisms associated with intervertebral disc degeneration

المؤلفون: Serkan Kitiş, Pelin Tasdemir, Ayse Gul Zamani, Aynur Acar, Ebru Tuncez, Zeynep Mine Coskun

المساهمون: KİTİŞ, SERKAN

المصدر: Cellular and Molecular Biology. 64:61-65

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Genotype, Turkey, Kitis S., COSKUN Z., TASDEMIR P., TUNCEZ E., ZAMANI A., ACAR A., -Analysis of genetic polymorphisms associated with intervertebral disc degeneration.-, Cellular and molecular biology (Noisy-le-Grand, France), cilt.64, ss.61-65, 2018, medicine.medical_treatment, Intervertebral Disc Degeneration, Biology, Calcitriol receptor, Receptor, IGF Type 1, 03 medical and health sciences, Insulin-like growth factor, 0302 clinical medicine, Internal medicine, medicine, Humans, Allele, Gene, Insulin-like growth factor 1 receptor, Polymorphism, Genetic, Receptors, Somatomedin, Intervertebral disc, General Medicine, Middle Aged, Endocrinology, medicine.anatomical_structure, 030220 oncology & carcinogenesis, Matrix Metalloproteinase 2, Receptors, Calcitriol, Female, Gene polymorphism, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d7369038d9df92d7c0153cfc75eaaf8Test
https://doi.org/10.14715/cmb/2018.64.10.10Test

8

Meta-genome-wide association studies identify a locus on chromosome 1 and multiple variants in the MHC region for serum C-peptide in type 1 diabetes

المؤلفون: Andrew D. Paterson, Shelley B. Bull, Hillary A. Keenan, Delnaz Roshandel, Rose Gubitosi-Klug, Ronald Klein, Barbara E.K. Klein, Angelo J. Canty, Michael N. Weedon, George L. King, Janet K. Snell-Bergeon, Marcus G. Pezzolesi, Tina Costacou, Richard A. Oram, Trevor J. Orchard, David M. Maahs

المصدر: Diabetologia

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Genome-wide association study, medicine.medical_specialty, Adolescent, Genotype, Endocrinology, Diabetes and Metabolism, Locus (genetics), Single-nucleotide polymorphism, Major histocompatibility complex, Polymorphism, Single Nucleotide, Article, Young Adult, 03 medical and health sciences, Gene Frequency, Internal medicine, Internal Medicine, medicine, Humans, Genetic Predisposition to Disease, Allele, Allele frequency, Alleles, Type 1 diabetes, C-Peptide, biology, Insulin-secreting cells, Histocompatibility Antigens Class I, medicine.disease, Single nucleotide polymorphism, 3. Good health, Minor allele frequency, Cross-Sectional Studies, Diabetes Mellitus, Type 1, 030104 developmental biology, Endocrinology, Chromosomes, Human, Pair 1, biology.protein, Female

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14180d6dbba4f52f5e1945969049c8a7Test
https://doi.org/10.1007/s00125-018-4555-9Test

9

Association of sirtuin 1 gene polymorphisms with nephrolithiasis in Eastern chinese population

المؤلفون: Lu Li, Xiaofeng Gao, Jiarong Ding, Jiebin Hou, Yonghan Peng, Zhiyong Guo

المصدر: Renal Failure
Renal Failure, Vol 41, Iss 1, Pp 34-41 (2019)

مصطلحات موضوعية: Male, Linkage disequilibrium, endocrine system diseases, Mice, Knockout, ApoE, 030232 urology & nephrology, 030204 cardiovascular system & hematology, Critical Care and Intensive Care Medicine, Linkage Disequilibrium, Mice, 0302 clinical medicine, Sirtuin 1, single nucleotide polymorphism, Kidney, biology, Incidence, General Medicine, Middle Aged, kidney stone, Kidney Tubules, medicine.anatomical_structure, Nephrology, Female, lipids (amino acids, peptides, and proteins), biological phenomena, cell phenomena, and immunity, SIRT1 Gene, hormones, hormone substitutes, and hormone antagonists, Adult, medicine.medical_specialty, Genotype, Single-nucleotide polymorphism, Nephrolithiasis, Polymorphism, Single Nucleotide, 03 medical and health sciences, SIRT1, Asian People, Internal medicine, medicine, Animals, Humans, Genetic Predisposition to Disease, Chinese, Calcium Oxalate, business.industry, Haplotype, Case-control study, CaOx crystal, medicine.disease, Diseases of the genitourinary system. Urology, Mice, Inbred C57BL, Disease Models, Animal, enzymes and coenzymes (carbohydrates), Endocrinology, Case-Control Studies, Clinical Study, biology.protein, Kidney stones, RC870-923, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02cd3b171643327ca83d1ea8c6509724Test
https://doi.org/10.1080/0886022x.2019.1568258Test

10

Role of PON1, SOD2, OGG1, XRCC1, and XRCC4 polymorphisms on modulation of DNA damage in workers occupationally exposed to pesticides

المؤلفون: Daniel Simon, Claudia Telles de Souza, Varinderpal S. Dhillon, Melissa Rosa de Souza, Juliana Picinini, Michael Fenech, Flávia Valadão Thiesen, Mirian Salvador, Cátia dos Santos Branco, Juliana da Silva, Fernanda Rabaioli da Silva, Jodel Alves, Vivian Francília Silva Kahl, Gabrieli Flesch da Silva, Johnny Ferraz Dias

المصدر: Ecotoxicology and Environmental Safety. 159:164-171

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, medicine.medical_specialty, Genotype, DNA damage, Health, Toxicology and Mutagenesis, DNA Glycosylases, Superoxide dismutase, 03 medical and health sciences, XRCC1, 0302 clinical medicine, Occupational Exposure, Internal medicine, Tobacco, medicine, Humans, Pesticides, Farmers, Micronucleus Tests, Polymorphism, Genetic, biology, Aryldialkylphosphatase, Superoxide Dismutase, Public Health, Environmental and Occupational Health, Paraoxonase, General Medicine, Middle Aged, DNA repair protein XRCC4, Pollution, PON1, DNA-Binding Proteins, Comet assay, X-ray Repair Cross Complementing Protein 1, 030104 developmental biology, Endocrinology, DNA glycosylase, 030220 oncology & carcinogenesis, biology.protein, Female, Comet Assay, DNA Damage

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17f751b27787481be235969db6d6867eTest
https://doi.org/10.1016/j.ecoenv.2018.04.052Test

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