نتائج البحث - "Genetics, Genomics, and Proteomics"

1

Association between Insertion-Deletion Polymorphism of the Angiotensin-Converting Enzyme Gene and Treatment Response to Antipsychotic Medications: A Study of Antipsychotic-Naïve First-Episode Psychosis Patients and Nonadherent Chronic Psychosis Patients

المؤلفون: Sergej Nadalin, Sanja Dević Pavlić, Vjekoslav Peitl, Dalibor Karlović, Lena Zatković, Smiljana Ristić, Alena Buretić-Tomljanović, Hrvoje Jakovac

المصدر: International Journal of Molecular Sciences
Volume 23
Issue 20
International Journal of Molecular Sciences; Volume 23; Issue 20; Pages: 12180

مصطلحات موضوعية: Male, Angiotensins, Genotype, BIOMEDICINE AND HEALTHCARE. Basic Medical Sciences. Immunology, Peptidyl-Dipeptidase A, Catalysis, angiotensin‐converting enzyme (ACE), polymorphism, Inorganic Chemistry, BIOMEDICINA I ZDRAVSTVO. Kliničke medicinske znanosti. Psihijatrija, BIOMEDICINE AND HEALTHCARE. Basic Medical Sciences. Human Genetics, Genomics and Proteomics, Humans, Physical and Theoretical Chemistry, Molecular Biology, Spectroscopy, Metabolic Syndrome, psychiatry_mental_health_studies, Organic Chemistry, treatment response, General Medicine, BIOMEDICINE AND HEALTHCARE. Clinical Medical Sciences. Psychiatry, Lipids, antipsychotic medication, Computer Science Applications, angiotensin-converting enzyme (ACE), insertion/deletion, Glucose, Psychotic Disorders, BIOMEDICINA I ZDRAVSTVO. Temeljne medicinske znanosti. Imunologija, Female, BIOMEDICINA I ZDRAVSTVO. Temeljne medicinske znanosti. Genetika, genomika i proteomika čovjeka, Antipsychotic Agents

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b327280c1300f31771ba3a0e2cf54733Test
https://repository.medri.uniri.hr/islandora/object/medri:6914Test

2

Genetic and epigenetic profiling indicates the proximal tubule origin of renal cancers in end‐stage renal disease

المؤلفون: Sekiko Taneda, Yoji Nagashima, Kazuhiko Yoshida, Kazunari Tanabe, Tsunenori Kondo, Naoko Hattori, Toshio Takagi, Satoshi Yamashita, Toshikazu Ushijima, Omar El-Omar, Hironori Fukuda, Yu-Yu Liu, Hiroki Ishihara, Takashi Ikeda

المصدر: Cancer Science

مصطلحات موضوعية: Male, 0301 basic medicine, Cancer Research, Nephron, Chromophobe cell, urologic and male genital diseases, Epigenesis, Genetic, Kidney Tubules, Proximal, Epigenome, 0302 clinical medicine, Renal cell carcinoma, Genetics, Genomics, and Proteomics, BAP1, hemodialysis, kidney cancer, General Medicine, Middle Aged, Immunohistochemistry, Kidney Neoplasms, female genital diseases and pregnancy complications, medicine.anatomical_structure, Oncology, 030220 oncology & carcinogenesis, DNA methylation, Original Article, Female, Adult, renal cell carcinoma, DNA Copy Number Variations, Genotype, Biology, End stage renal disease, 03 medical and health sciences, Chromosome 16, medicine, Humans, Genetic Predisposition to Disease, Epigenetics, Carcinoma, Renal Cell, Aged, epigenetics, Gene Expression Profiling, Original Articles, medicine.disease, 030104 developmental biology, ACD‐RCC, Mutation, Cancer research, Kidney Failure, Chronic, Transcriptome

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b81dd00d6c76e31d8743ce9fb4378bd8Test
https://doi.org/10.1111/cas.14633Test

3

Potential protective role of a NOD2 polymorphism in the susceptibility to multiple sclerosis is not associated with interferon therapy

المؤلفون: Nada Starčević Čizmarević, Luca Lovrečić, Aleš Maver, Borut Peterlin, Aida Zečkanović, Smiljana Ristić

المصدر: Biomed Rep
Biomedical Reports
Volume 15
Issue 6

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1f416737efa546dbe3a6ec39e0580feTest
https://pubmed.ncbi.nlm.nih.gov/34667597Test

4

NOTCH1 pathway activating mutations and clonal evolution in pediatric T‐cell acute lymphoblastic leukemia

المؤلفون: Shunsuke Kimura, Kenichi Yoshida, Katsuyoshi Koh, Yuichi Shiraishi, Akira Oka, Seishi Ogawa, Atsushi Manabe, Yasuhide Hayashi, Toshihiko Imamura, Satoru Miyano, Masaharu Akiyama, Junko Takita, Masafumi Seki, Masao Kobayashi

المصدر: Cancer Science

مصطلحات موضوعية: 0301 basic medicine, Male, Cancer Research, F-Box-WD Repeat-Containing Protein 7, Adolescent, Genotype, T cell, T-Lymphocytes, Clone (cell biology), Disease, Precursor T-Cell Lymphoblastic Leukemia-Lymphoma, Somatic evolution in cancer, Polymorphism, Single Nucleotide, Deep sequencing, Clonal Evolution, 03 medical and health sciences, 0302 clinical medicine, NOTCH1, Recurrence, hemic and lymphatic diseases, T‐cell acute lymphoblastic leukemia, medicine, Humans, Receptor, Notch1, Child, Genetics, Genomics, and Proteomics, Exome sequencing, relapse, business.industry, High-Throughput Nucleotide Sequencing, General Medicine, Original Articles, Amplicon, 030104 developmental biology, medicine.anatomical_structure, Oncology, 030220 oncology & carcinogenesis, Child, Preschool, Cohort, Mutation, Cancer research, Original Article, pediatric leukemia, Female, business, whole–exome sequencing, Signal Transduction

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9eaa0b69ea8434fb004379736ab6baf5Test
http://europepmc.org/articles/PMC6361559Test

5

Prevalence of rare F5 variants in general population from Bosnia and Herzegovina

المؤلفون: Adna Ašić, Ramona Salazar, Damir Marjanović, Dragan Primorac, Serkan Dogan, Wolfgang Höppner, Niels Storm

المصدر: Molecular Biology Reports
Volume 48
Issue 6

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9ee6c0348a552bccfc529dd6d2422f0Test
https://www.bib.irb.hr/1250739Test

6

ACE I/D polymorphism and epidemiological findings for COVID-19: One year after the pandemic outbreak in Europe

المؤلفون: Smiljana Ristić, Sanja Dević Pavlić, Sergej Nadalin, Nada Starčević Čizmarević

المصدر: Journal of Infection
Volume 83
Issue 3

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4acd49a0b1f5f9558c9008724535e26Test
https://www.bib.irb.hr/1140010Test

7

Rapid and sensitive detection of UGT1A1 polymorphisms associated with irinotecan toxicity by a novel DNA microarray

المؤلفون: Naoko Okayama, Hiroaki Nagano, Shoichi Hazama, Ryouichi Tsunedomi, Masaaki Oka

المصدر: Cancer Science

مصطلحات موضوعية: 0301 basic medicine, Cancer Research, Genotype, Colorectal cancer, precision medicine, Computational biology, Biology, Irinotecan, Polymorphism, Single Nucleotide, polymorphism, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, medicine, Humans, Genetic Predisposition to Disease, in vitro diagnostics, Genetic Testing, Glucuronosyltransferase, Genotyping, Genetics, Genomics, and Proteomics, Oligonucleotide Array Sequence Analysis, business.industry, DNA microarray, General Medicine, Original Articles, medicine.disease, Precision medicine, Molecular biology, Antineoplastic Agents, Phytogenic, 030104 developmental biology, Oncology, chemistry, 030220 oncology & carcinogenesis, Toxicity, Original Article, Camptothecin, Personalized medicine, business, Colorectal Neoplasms, DNA, medicine.drug

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9636c41b208dabc4b973de458f23f2d8Test
http://europepmc.org/articles/PMC5497725Test

8

Association between PLA2G6 gene polymorphism for calcium-independent phospholipase A2 and nicotine dependence among males with schizophrenia

المؤلفون: Jelena Rebić, Vjekoslav Peitl, Dalibor Karlović, Vesna Šendula Jengić, Alena Buretić-Tomljanović, Sergej Nadalin

المصدر: Prostaglandins, Leukotrienes and Essential Fatty Acids
Volume 148

مصطلحات موضوعية: Male, 0301 basic medicine, Clinical Biochemistry, phospholipase A2, polymorphism, schizophrenia, smoking, DOPAMINE, 0302 clinical medicine, BIOMEDICINE AND HEALTHCARE. Basic Medical Sciences. Human Genetics, Genomics and Proteomics, Polymorphism (computer science), Phospholipase A2, Genotype, Medicine, Age of Onset, BRAIN, POLYUNSATURATED FATTY-ACIDS, Sex Characteristics, Positive and Negative Syndrome Scale, biology, Smoking, Tobacco Use Disorder, Middle Aged, Schizophrenia, Female, BIOMEDICINA I ZDRAVSTVO. Temeljne medicinske znanosti. Genetika, genomika i proteomika čovjeka, Psychopathology, Adult, phospholipase A2, polymorphism, schizophrenia, smoking, medicine.medical_specialty, Croatia, 030209 endocrinology & metabolism, Polymorphism, Single Nucleotide, Group VI Phospholipases A2, 03 medical and health sciences, BIOMEDICINA I ZDRAVSTVO. Kliničke medicinske znanosti. Psihijatrija, Polymorphism, POSTMORTEM ORBITOFRONTAL CORTEX, DOCOSAHEXAENOIC ACID, CIGARETTE-SMOKING, BANI POLYMORPHISM, A(2) ACTIVITY, ALLELIC ASSOCIATION, TOBACCO SMOKING, Internal medicine, Humans, Allele, Genetic Association Studies, 030109 nutrition & dietetics, business.industry, Group IV Phospholipases A2, Cell Biology, BIOMEDICINE AND HEALTHCARE. Clinical Medical Sciences. Psychiatry, medicine.disease, PLA2G4A, Endocrinology, biology.protein, Gene polymorphism, business

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::350215fa47511dc118834130129d1a1cTest
https://www.bib.irb.hr/1048540Test

9

Population study of thrombophilic markers and pharmacogenetic markers of warfarin prevalence in Bosnia and Herzegovina

المؤلفون: Damir Marjanović, Adna Ašić, Ramona Salazar, Wolfgang Höppner, Niels Storm, Dragan Primorac, Serkan Dogan

المصدر: Croatian Medical Journal
Volume 60
Issue 3

مصطلحات موضوعية: Male, pharmacogenetic markers, Gastroenterology, Thrombophilic markers, 0302 clinical medicine, BIOMEDICINE AND HEALTHCARE. Basic Medical Sciences. Human Genetics, Genomics and Proteomics, Gene Frequency, Pregnancy, Medicine, Thrombophilia, 030212 general & internal medicine, BIOMEDICINA I ZDRAVSTVO. Kliničke medicinske znanosti. Interna medicina, education.field_of_study, biology, Factor XIII, General Medicine, Middle Aged, Blood Coagulation Factors, Female, Prothrombin, VKORC1, BIOMEDICINA I ZDRAVSTVO. Temeljne medicinske znanosti. Genetika, genomika i proteomika čovjeka, medicine.drug, Adult, medicine.medical_specialty, Adolescent, Genotype, Population, 03 medical and health sciences, Young Adult, 11th ISABS CONFERENCE, Internal medicine, Vitamin K Epoxide Reductases, thrombophilic markers, warfarin, Plasminogen Activator Inhibitor 1, Factor V Leiden, Humans, education, Allele frequency, BIOMEDICINE AND HEALTHCARE. Clinical Medical Sciences. Internal Medicine, Alleles, Methylenetetrahydrofolate Reductase (NADPH2), Cytochrome P-450 CYP2C9, Bosnia and Herzegovina, business.industry, Warfarin, Anticoagulants, Factor V, medicine.disease, Methylenetetrahydrofolate reductase, biology.protein, business, Pharmacogenetics, Biomarkers

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7b18db477761808c54dcf1611ee72b0Test
https://urn.nsk.hr/urn:nbn:hr:184:188436Test

10

Maternal LINE-1 DNA Methylation and Congenital Heart Defects in Down Syndrome

المؤلفون: Maja Živković, Jadranka Vraneković, Bojana Brajenović-Milić, Ivana Babić Božović, Aleksandra Stanković, Vesna Mahulja-Stamenković

المصدر: Frontiers in Genetics
Chromosome Research
Volume 10
Frontiers in Genetics, Vol 10 (2019)

مصطلحات موضوعية: 0301 basic medicine, Down syndrome, lcsh:QH426-470, Physiology, Overweight, 03 medical and health sciences, symbols.namesake, LINE-1, 0302 clinical medicine, BIOMEDICINE AND HEALTHCARE. Basic Medical Sciences. Human Genetics, Genomics and Proteomics, LINE-1 methylation, congenital heart defects, Genotype, Genetics, Medicine, Genotyping, Genetics (clinical), Original Research, 2. Zero hunger, DNA methylation, business.industry, Methylation, medicine.disease, 3. Good health, lcsh:Genetics, 030104 developmental biology, Bonferroni correction, 030220 oncology & carcinogenesis, symbols, maternal risk, Molecular Medicine, medicine.symptom, business, Body mass index, BIOMEDICINA I ZDRAVSTVO. Temeljne medicinske znanosti. Genetika, genomika i proteomika čovjeka

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d0ca449ac710a4c6e2799106562e830Test
https://vinar.vin.bg.ac.rs/handle/123456789/8208Test

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