Temat: "Polymorphism, Single Nucleotide" - OpacWWW

Skocz do pozycji: 1 1.

Tytuł :: Overwhelming mutations or SNPs of SARS-CoV-2: A point of caution.
Autorzy :: Vankadari N; Monash Biomedicine Discovery Institute and Department of Biochemistry and Molecular Biology, Monash University, Victoria 3800, Australia. Electronic address: .; Pokaż więcej
Źródło :: Gene [Gene] 2020 Aug 20; Vol. 752, pp. 144792. Date of Electronic Publication: 2020 May 20.
Typ publikacji :: Letter
Journal Info :: Publisher: Elsevier/North-Holland Country of Publication: Netherlands NLM ID: 7706761 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-0038 (Electronic) Linking ISSN: 03781119 NLM ISO Abbreviation: Gene Subsets: MEDLINE
MeSH Terms :: Point Mutation*
Polymorphism, Single Nucleotide*
Betacoronavirus/*genetics
Americas/epidemiology ; Asia/epidemiology ; Coronavirus Infections/epidemiology ; Coronavirus Infections/virology ; Drug Resistance, Viral ; Europe/epidemiology ; Genome, Viral ; Humans ; Pandemics ; Phylogeny ; Pneumonia, Viral/epidemiology ; Pneumonia, Viral/virology ; Spike Glycoprotein, Coronavirus/genetics ; Viral Proteins/classification ; Viral Proteins/genetics
SCR Disease Name :: COVID-19
SCR Organism :: severe acute respiratory syndrome coronavirus 2
: Opinia redakcyjna

Szczegóły

Skocz do pozycji: 2 2.

Tytuł :: The Contribution of MMP-9 Genotypes to Pterygium in Taiwan.
Autorzy :: Tsai CB; Department of Ophthalmology, Chia-Yi Christian Hospital, Chia-Yi, Taiwan, R.O.C.
Hsia NY; Department of Ophthalmology, China Medical University Hospital, Taichung, Taiwan, R.O.C.; Terry Fox Cancer Research Laboratory, Department of Medical Research, China Medical University Hospital, Taichung, Taiwan, R.O.C.
Wang ZH; Department of Food Nutrition and Health Biotechnology, Asia University, Taichung, Taiwan, R.O.C.
Yang JS; Terry Fox Cancer Research Laboratory, Department of Medical Research, China Medical University Hospital, Taichung, Taiwan, R.O.C.; Department of Medical Research, China Medical University Hospital, Taichung, Taiwan, R.O.C.
Hsu YM; Department of Biological Science and Technology, China Medical University, Taichung, Taiwan, R.O.C.
Wang YC; Terry Fox Cancer Research Laboratory, Department of Medical Research, China Medical University Hospital, Taichung, Taiwan, R.O.C.
Chang WS; Terry Fox Cancer Research Laboratory, Department of Medical Research, China Medical University Hospital, Taichung, Taiwan, R.O.C.
Bau DT; Terry Fox Cancer Research Laboratory, Department of Medical Research, China Medical University Hospital, Taichung, Taiwan, R.O.C. .; Department of Bioinformatics and Medical Engineering, Asia University, Taichung, Taiwan, R.O.C.
Yin MC; Department of Food Nutrition and Health Biotechnology, Asia University, Taichung, Taiwan, R.O.C. .
Tsai CW; Terry Fox Cancer Research Laboratory, Department of Medical Research, China Medical University Hospital, Taichung, Taiwan, R.O.C. .; Pokaż więcej
Źródło :: Anticancer research [Anticancer Res] 2020 Aug; Vol. 40 (8), pp. 4523-4527.
Typ publikacji :: Journal Article
Journal Info :: Publisher: International Institute of Anticancer Research Country of Publication: Greece NLM ID: 8102988 Publication Model: Print Cited Medium: Internet ISSN: 1791-7530 (Electronic) Linking ISSN: 02507005 NLM ISO Abbreviation: Anticancer Res. Subsets: MEDLINE
MeSH Terms :: Polymorphism, Single Nucleotide*
Asian Continental Ancestry Group/*genetics
Matrix Metalloproteinase 9/*genetics
Pterygium/*genetics
Aged ; Aged, 80 and over ; Case-Control Studies ; Female ; Gene Frequency ; Genetic Association Studies ; Genetic Predisposition to Disease ; Genotype ; Humans ; Male ; Middle Aged ; Prognosis ; Promoter Regions, Genetic ; Pterygium/diagnosis ; Taiwan
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 3 3.

Tytuł :: MiR-196a-2 Genotypes Determine the Susceptibility and Early Onset of Childhood Acute Lymphoblastic Leukemia.
Autorzy :: Chen CC; Department of Pediatrics, Taoyuan General Hospital, Ministry of Health and Welfare, Taoyuan, Taiwan, R.O.C.
Hsu PC; Department of Pediatrics, Taoyuan General Hospital, Ministry of Health and Welfare, Taoyuan, Taiwan, R.O.C.
Shih LC; Department of Medical Research, Terry Fox Cancer Research Laboratory, China Medical University Hospital, Taichung, Taiwan, R.O.C.; Department of Otorhinolaryngology, China Medical University Hospital, Taichung, Taiwan, R.O.C.
Hsu YN; Department of Family Medicine, Taoyuan General Hospital, Ministry of Health and Welfare, Taoyuan, Taiwan, R.O.C.
Kuo CC; Department of Pediatric Orthopedics, China Medical University Hospital, Taichung, Taiwan, R.O.C.
Chao CY; Department of Food Nutrition and Health Biotechnology, Asia University, Taichung, Taiwan, R.O.C.
Chang WS; Department of Medical Research, Terry Fox Cancer Research Laboratory, China Medical University Hospital, Taichung, Taiwan, R.O.C.; Graduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan, R.O.C.
Tsai CW; Department of Medical Research, Terry Fox Cancer Research Laboratory, China Medical University Hospital, Taichung, Taiwan, R.O.C.; Graduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan, R.O.C.
Bau DT; Department of Medical Research, Terry Fox Cancer Research Laboratory, China Medical University Hospital, Taichung, Taiwan, R.O.C. .; Graduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan, R.O.C.; Department of Bioinformatics and Medical Engineering, Asia University, Taichung, Taiwan, R.O.C.
Pei JS; Department of Pediatrics, Taoyuan General Hospital, Ministry of Health and Welfare, Taoyuan, Taiwan, R.O.C. .; Pokaż więcej
Źródło :: Anticancer research [Anticancer Res] 2020 Aug; Vol. 40 (8), pp. 4465-4469.
Typ publikacji :: Journal Article
Journal Info :: Publisher: International Institute of Anticancer Research Country of Publication: Greece NLM ID: 8102988 Publication Model: Print Cited Medium: Internet ISSN: 1791-7530 (Electronic) Linking ISSN: 02507005 NLM ISO Abbreviation: Anticancer Res. Subsets: MEDLINE
MeSH Terms :: Polymorphism, Single Nucleotide*
Asian Continental Ancestry Group/*genetics
MicroRNAs/*genetics
Precursor Cell Lymphoblastic Leukemia-Lymphoma/*genetics
Adolescent ; Age of Onset ; Case-Control Studies ; Child ; Child, Preschool ; Female ; Genetic Association Studies ; Genetic Predisposition to Disease ; Genotype ; Humans ; Male ; Taiwan
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 4 4.

Tytuł :: Genetic variations of CARMN affect risk of esophageal cancer in northwest China.
Autorzy :: Jia A; Department of Digestive System, the First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi 710061, China.
Wu Y; Department of Operation, the First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi 710061, China.
Ren W; Department of Otolaryngology & Head Neck, the First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi 710061, China.
Han P; Department of Otolaryngology & Head Neck, the First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi 710061, China. Electronic address: .
Shao Y; Department of Otolaryngology & Head Neck, the First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi 710061, China. Electronic address: .; Pokaż więcej
Źródło :: Gene [Gene] 2020 Jul 20; Vol. 748, pp. 144680. Date of Electronic Publication: 2020 Apr 17.
Typ publikacji :: Journal Article
Journal Info :: Publisher: Elsevier/North-Holland Country of Publication: Netherlands NLM ID: 7706761 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-0038 (Electronic) Linking ISSN: 03781119 NLM ISO Abbreviation: Gene Subsets: MEDLINE
MeSH Terms :: Genetic Predisposition to Disease*
Polymorphism, Single Nucleotide*
Esophageal Neoplasms/*genetics
RNA, Long Noncoding/*genetics
Aged ; China/epidemiology ; Female ; Haplotypes ; Humans ; Male ; Middle Aged
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 5 5.

Tytuł :: Decisive evidence corroborates a null relationship between MTHFR C677T and chronic kidney disease: A case-control study and a meta-analysis.
Autorzy :: Chang HL; aSchool of Public Health bSchool of Dentistry cCenter for General Education, National Defense Medical Center, Taipei dDepartment of Internal Medicine, Taoyuan Armed Forces General Hospital eDivision of Infectious Diseases, Department of Internal Medicine, Taoyuan Armed Forces General Hospital, National Defense Medical Center, Taoyuan fDepartment of Ophthalmology, Tri-Service General Hospital, National Defense Medical Center, Taipei gDepartment of Emergency Medicine, Taoyuan Armed Forces General Hospital, National Defense Medical Center, Taoyuan hGraduate Institute of Life Sciences, National Defense Medical Center, Taipei iDepartment of Health Industry Management, Kainan University, Taoyuan jDivision of Thoracic Medicine, Department of Medicine, Cheng Hsin General Hospital kDepartment of Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan, ROC.
Chen GR
Hsiao PJ
Chiu CC
Tai MC
Kao CC
Tsai DJ
Su H
Chen YH
Chen WT
Su SL; Pokaż więcej
Źródło :: Medicine [Medicine (Baltimore)] 2020 Jul 17; Vol. 99 (29), pp. e21045.
Typ publikacji :: Journal Article; Meta-Analysis; Systematic Review
Journal Info :: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 2985248R Publication Model: Print Cited Medium: Internet ISSN: 1536-5964 (Electronic) Linking ISSN: 00257974 NLM ISO Abbreviation: Medicine (Baltimore) Subsets: Core Clinical (AIM); MEDLINE
MeSH Terms :: Polymorphism, Single Nucleotide*
Methylenetetrahydrofolate Reductase (NADPH2)/*genetics
Renal Insufficiency, Chronic/*genetics
Aged ; Asian Continental Ancestry Group/genetics ; Case-Control Studies ; European Continental Ancestry Group/genetics ; Female ; Gene-Environment Interaction ; Genetic Predisposition to Disease ; Humans ; Male ; Taiwan
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 6 6.

Tytuł :: Genetic polymorphisms in serine protease inhibitor Kazal-type 5 and risk of atopic dermatitis: A meta-analysis.
Autorzy :: Li Y; Department of Dermatology, Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou 310052, Zhejiang Province, China.
Li Y
Li W
Guo X
Zhou S
Zheng H; Pokaż więcej
Źródło :: Medicine [Medicine (Baltimore)] 2020 Jul 10; Vol. 99 (28), pp. e21256.
Typ publikacji :: Journal Article; Meta-Analysis
Journal Info :: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 2985248R Publication Model: Print Cited Medium: Internet ISSN: 1536-5964 (Electronic) Linking ISSN: 00257974 NLM ISO Abbreviation: Medicine (Baltimore) Subsets: Core Clinical (AIM); MEDLINE
MeSH Terms :: Polymorphism, Single Nucleotide*
Dermatitis, Atopic/*genetics
Genetic Predisposition to Disease/*genetics
Serine Peptidase Inhibitor Kazal-Type 5/*genetics
Adolescent ; Adult ; Aged ; Child ; Female ; Genotyping Techniques ; Humans ; Male ; Middle Aged ; Risk Factors ; Young Adult
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 7 7.

Tytuł :: Correlation of Tumor Necrosis Factor-α -308G>A Polymorphism with Susceptibility, Clinical Manifestations, and Severity in Behçet Syndrome: Evidences from an Italian Genetic Case-Control Study.
Autorzy :: Padula MC; Rheumatology Institute of Lucania (IReL), San Carlo Hospital of Potenza and Madonna delle Grazie Hospital of Matera, Potenza, Italy.; Department of Science, University of Basilicata, Potenza, Italy.
Leccese P; Rheumatology Institute of Lucania (IReL), San Carlo Hospital of Potenza and Madonna delle Grazie Hospital of Matera, Potenza, Italy.
Lascaro N; Rheumatology Institute of Lucania (IReL), San Carlo Hospital of Potenza and Madonna delle Grazie Hospital of Matera, Potenza, Italy.
Radice RP; Department of Science, University of Basilicata, Potenza, Italy.; Bioinnova srls, Potenza, Italy.
Limongi AR; Department of Science, University of Basilicata, Potenza, Italy.; Bioinnova srls, Potenza, Italy.
Sorrento GG; Department of Science, University of Basilicata, Potenza, Italy.
Carbone T; Rheumatology Institute of Lucania (IReL), San Carlo Hospital of Potenza and Madonna delle Grazie Hospital of Matera, Potenza, Italy.
Padula AA; Rheumatology Institute of Lucania (IReL), San Carlo Hospital of Potenza and Madonna delle Grazie Hospital of Matera, Potenza, Italy.
Martelli G; Department of Science, University of Basilicata, Potenza, Italy.
D'Angelo S; Rheumatology Institute of Lucania (IReL), San Carlo Hospital of Potenza and Madonna delle Grazie Hospital of Matera, Potenza, Italy.; Pokaż więcej
Źródło :: DNA and cell biology [DNA Cell Biol] 2020 Jul; Vol. 39 (7), pp. 1104-1110. Date of Electronic Publication: 2020 Apr 29.
Typ publikacji :: Journal Article
Journal Info :: Publisher: Mary Ann Liebert Country of Publication: United States NLM ID: 9004522 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1557-7430 (Electronic) Linking ISSN: 10445498 NLM ISO Abbreviation: DNA Cell Biol. Subsets: MEDLINE
MeSH Terms :: Polymorphism, Single Nucleotide*
Behcet Syndrome/*genetics
Genetic Predisposition to Disease/*genetics
Tumor Necrosis Factor-alpha/*genetics
Case-Control Studies ; Female ; Humans ; Italy ; Male ; Middle Aged
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 8 8.

Tytuł :: No Significant Effects of IL-6 and IL-13 Gene Variants on Tuberculosis Susceptibility in the Chinese Population.
Autorzy :: Sun W; Department of Laboratory Medicine, Guiyang Children's Hospital, Guiyang, China.
Jiao L; Department of Laboratory Medicine, West China Hospital of Sichuan University, Chengdu, China.
Liu T; Department of Laboratory Medicine, West China Hospital of Sichuan University, Chengdu, China.
Song J; Department of Laboratory Medicine, West China Hospital of Sichuan University, Chengdu, China.
Wang M; Department of Laboratory Medicine, West China Hospital of Sichuan University, Chengdu, China.
Liang L; Department of Laboratory Medicine, Guiyang Children's Hospital, Guiyang, China.
Wen C; Department of Laboratory Medicine, Guiyang Children's Hospital, Guiyang, China.
Hu L; Department of Laboratory Medicine, Guiyang Children's Hospital, Guiyang, China.
Qu W; Department of Laboratory Medicine, Guiyang Children's Hospital, Guiyang, China.
Ying B; Department of Laboratory Medicine, West China Hospital of Sichuan University, Chengdu, China.; Pokaż więcej
Źródło :: DNA and cell biology [DNA Cell Biol] 2020 Jul; Vol. 39 (7), pp. 1356-1367. Date of Electronic Publication: 2020 Jun 09.
Typ publikacji :: Journal Article
Journal Info :: Publisher: Mary Ann Liebert Country of Publication: United States NLM ID: 9004522 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1557-7430 (Electronic) Linking ISSN: 10445498 NLM ISO Abbreviation: DNA Cell Biol. Subsets: MEDLINE
MeSH Terms :: Polymorphism, Single Nucleotide*
Genetic Predisposition to Disease/*genetics
Interleukin-13/*genetics
Interleukin-6/*genetics
Tuberculosis/*genetics
Case-Control Studies ; China/epidemiology ; Haplotypes/genetics ; Humans ; Tuberculosis/epidemiology
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 9 9.

Tytuł :: The rs46522 Polymorphism of the Ubiquitin-Conjugating Enzyme E2Z Gene Is Associated with Abnormal Metabolic Parameters in Patients with Myocardial Infarction: The Genetics of Atherosclerosis Disease Mexican Study.
Autorzy :: Rodríguez-Pérez JM; Department of Molecular Biology and Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
Posadas-Sánchez R; Department of Endocrinology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
Vargas-Alarcón G; Department of Molecular Biology and Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
Blachman-Braun R; Department of Urology, University of Miami Miller School of Medicine, Miami, Florida, USA.
García-Flores E; Department of Molecular Biology and Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
Cazarín-Santos BG; Department of Molecular Biology and Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
Castillo-Avila RG; Department of Molecular Biology and Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.; Academic Division of Health Sciences, Universidad Juárez Autónoma de Tabasco, Villahermosa, Tabasco, Mexico.
Borgonio-Cuadra VM; Department of Genetics, Instituto Nacional de Rehabilitación Luis Guillermo Ibarra Ibarra, Mexico City, Mexico.
Tovilla-Zárate CA; Multidisciplinary Academic Division of Comalcalco, Universidad Juárez Autónoma de Tabasco, Comalcalco, Tabasco, Mexico.
González-Castro TB; Multidisciplinary Academic Division of Jalpa de Méndez, Universidad Juárez Autónoma de Tabasco, Jalpa de Méndez, Tabasco, Mexico.
López-Bautista F; Department of Endocrinology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
Pérez-Hernández N; Department of Molecular Biology and Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.; Pokaż więcej
Źródło :: DNA and cell biology [DNA Cell Biol] 2020 Jul; Vol. 39 (7), pp. 1155-1161. Date of Electronic Publication: 2020 May 11.
Typ publikacji :: Journal Article
Journal Info :: Publisher: Mary Ann Liebert Country of Publication: United States NLM ID: 9004522 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1557-7430 (Electronic) Linking ISSN: 10445498 NLM ISO Abbreviation: DNA Cell Biol. Subsets: MEDLINE
MeSH Terms :: Polymorphism, Single Nucleotide*
Atherosclerosis/*genetics
Myocardial Infarction/*genetics
Myocardial Infarction/*metabolism
Ubiquitin-Conjugating Enzymes/*genetics
Case-Control Studies ; Cohort Studies ; Female ; Humans ; Male ; Mexico/epidemiology ; Middle Aged ; Myocardial Infarction/epidemiology
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 10 10.

Tytuł :: miR-1262 Transcriptionally Modulated by an Enhancer Genetic Variant Improves Efficiency of Epidermal Growth Factor Receptor-Tyrosine Kinase Inhibitors in Advanced Lung Adenocarcinoma.
Autorzy :: Lei T; School of Medicine and Life Sciences, University of Jinan-Shandong Academy of Medical Sciences, Jinan, China.; Shandong Provincial Key Laboratory of Radiation Oncology, Cancer Research Center, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, China.
Zhang L; Department of Medical Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, China.
Song Y; School of Medicine and Life Sciences, University of Jinan-Shandong Academy of Medical Sciences, Jinan, China.; Shandong Provincial Key Laboratory of Radiation Oncology, Cancer Research Center, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, China.
Wang B; Shandong Provincial Key Laboratory of Radiation Oncology, Cancer Research Center, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, China.
Shen Y; Shandong Provincial Key Laboratory of Radiation Oncology, Cancer Research Center, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, China.
Zhang N; Department of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, China.
Yang M; Shandong Provincial Key Laboratory of Radiation Oncology, Cancer Research Center, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, China.; Pokaż więcej
Źródło :: DNA and cell biology [DNA Cell Biol] 2020 Jul; Vol. 39 (7), pp. 1111-1118. Date of Electronic Publication: 2020 Apr 27.
Typ publikacji :: Journal Article
Journal Info :: Publisher: Mary Ann Liebert Country of Publication: United States NLM ID: 9004522 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1557-7430 (Electronic) Linking ISSN: 10445498 NLM ISO Abbreviation: DNA Cell Biol. Subsets: MEDLINE
MeSH Terms :: Polymorphism, Single Nucleotide*
Adenocarcinoma of Lung/*genetics
Adenocarcinoma of Lung/*pathology
ErbB Receptors/*antagonists & inhibitors
Protein Kinase Inhibitors/*pharmacology
Transcription, Genetic/*drug effects
Alleles ; Cell Line, Tumor ; Cohort Studies ; Gefitinib/pharmacology ; Gene Expression Regulation, Neoplastic ; Humans ; Neoplasm Staging
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 11 11.

Tytuł :: Genome-wide association study of genetic variations associated with treatment failure after intravesical bacillus Calmette-Guérin therapy for non-muscle invasive bladder cancer.
Autorzy :: Shiota M; Department of Urology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan. .
Fujimoto N; Department of Urology, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, 807-8556, Japan.
Yamamoto Y; Department of Urology, Graduate School of Medicine, Yamaguchi University, Ube, 755-8505, Japan.
Takeuchi A; Department of Urology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.
Tatsugami K; Department of Urology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.
Uchiumi T; Department of Clinical Chemistry and Laboratory Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka, 812-8582, Japan.
Matsuyama H; Department of Urology, Graduate School of Medicine, Yamaguchi University, Ube, 755-8505, Japan.
Eto M; Department of Urology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.; Pokaż więcej
Źródło :: Cancer immunology, immunotherapy : CII [Cancer Immunol Immunother] 2020 Jul; Vol. 69 (7), pp. 1155-1163. Date of Electronic Publication: 2020 Mar 02.
Typ publikacji :: Journal Article
Journal Info :: Publisher: Springer Verlag Country of Publication: Germany NLM ID: 8605732 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-0851 (Electronic) Linking ISSN: 03407004 NLM ISO Abbreviation: Cancer Immunol. Immunother. Subsets: MEDLINE
MeSH Terms :: Genome-Wide Association Study*
Polymorphism, Single Nucleotide*
BCG Vaccine/*administration & dosage
Biomarkers, Tumor/*genetics
Urinary Bladder Neoplasms/*genetics
Administration, Intravesical ; Aged ; Disease Progression ; Female ; Follow-Up Studies ; Humans ; Male ; Middle Aged ; Retrospective Studies ; Survival Rate ; Treatment Failure ; Urinary Bladder Neoplasms/drug therapy ; Urinary Bladder Neoplasms/pathology
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 12 12.

Tytuł :: IL-12B Polymorphisms Are Associated with the Presence of Premature Coronary Artery Disease and with Cardiovascular Risk Factors: The Genetics of Atherosclerotic Disease Mexican Study.
Autorzy :: Vázquez-Vázquez C; Department of Molecular Biology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
Posadas-Sánchez R; Department of Endocrinology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
Fragoso JM; Department of Molecular Biology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.
Ramírez-Bello J; Research Unit on Endocrine and Metabolic Diseases, Hospital Juárez de México, Mexico City, Mexico.
Sánchez-Guerra M; Department of Developmental Neurobiology, Instituto Nacional de Perinatología, Mexico City, Mexico.
Osorio-Yañez C; Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de Mexico, Mexico City, Mexico.
Vargas-Alarcón G; Department of Molecular Biology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.; Pokaż więcej
Źródło :: DNA and cell biology [DNA Cell Biol] 2020 Jul; Vol. 39 (7), pp. 1347-1355. Date of Electronic Publication: 2020 Apr 29.
Typ publikacji :: Journal Article
Journal Info :: Publisher: Mary Ann Liebert Country of Publication: United States NLM ID: 9004522 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1557-7430 (Electronic) Linking ISSN: 10445498 NLM ISO Abbreviation: DNA Cell Biol. Subsets: MEDLINE
MeSH Terms :: Polymorphism, Single Nucleotide*
Atherosclerosis/*genetics
Coronary Artery Disease/*genetics
Interleukin-12 Subunit p40/*genetics
Coronary Artery Disease/epidemiology ; Female ; Genetic Predisposition to Disease/genetics ; Haplotypes ; Humans ; Male ; Mexico/epidemiology ; Middle Aged ; Risk Factors
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 13 13.

Tytuł :: Genetic variations in drug-metabolizing enzyme CYP2C9 among major ethnic groups of Pakistani population.
Autorzy :: Hizbullah; Department of Biochemistry, Abdul Wali Khan University Mardan (AWKUM), Mardan-23200, Khyber Pakhtunkhwa, Pakistan.
Ahmed S; Shifa College of Pharmaceutical Sciences, Shifa Tameer-e-Millat University, H-8/4, Islamabad.
Noor Mumtaz M; Department of Biochemistry, Abdul Wali Khan University Mardan (AWKUM), Mardan-23200, Khyber Pakhtunkhwa, Pakistan.
Zulfiqar Z; Shifa College of Pharmaceutical Sciences, Shifa Tameer-e-Millat University, H-8/4, Islamabad.
Amir Hamza S; Shifa College of Pharmaceutical Sciences, Shifa Tameer-e-Millat University, H-8/4, Islamabad.
Siraj S; Institute of Basic Medical Sciences, Khyber Medical University, Peshawar, Pakistan.
Jelani M; Center for Omics Sciences, Islamia College Peshawar, Pakistan.
Imran I; Department of Pharmacology, Faculty of Pharmacy, Bahauddin Zakariya University, Multan, Pakistan.
Khan A; Department of Biochemistry, Abdul Wali Khan University Mardan (AWKUM), Mardan-23200, Khyber Pakhtunkhwa, Pakistan. Electronic address: .; Pokaż więcej
Źródło :: Gene [Gene] 2020 Jul 01; Vol. 746, pp. 144659. Date of Electronic Publication: 2020 Apr 07.
Typ publikacji :: Clinical Trial; Journal Article
Journal Info :: Publisher: Elsevier/North-Holland Country of Publication: Netherlands NLM ID: 7706761 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-0038 (Electronic) Linking ISSN: 03781119 NLM ISO Abbreviation: Gene Subsets: MEDLINE
MeSH Terms :: Alternative Splicing*
Pharmacogenomic Variants*
Polymorphism, Single Nucleotide*
Cytochrome P-450 CYP2C9/*genetics
Ethnic Groups/*genetics
Cytochrome P-450 CYP2C9/metabolism ; Female ; Humans ; Male ; Pakistan/ethnology ; Warfarin/pharmacokinetics ; Warfarin/therapeutic use
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 14 14.

Tytuł :: Functional polymorphisms of BCL11A and HBS1L-MYB genes affect both fetal hemoglobin level and clinical outcomes in a cohort of children with sickle cell anemia.
Autorzy :: Sales RR; Programa de Pós-Graduação em Genética, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, Minas Gerais, Brazil. .; Programa de Pós-Graduação em Saúde da Criança e do Adolescente, Faculdade de Medicina, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, Minas Gerais, Brazil. .; Institute of Biological Sciences, Federal University of Minas Gerais (UFMG), Belo Horizonte, Minas Gerais, Brazil. .
Belisário AR; Centro de Tecidos Biológicos de Minas Gerais, Fundação Hemominas, Lagoa Santa, Minas Gerais, 33400-000, Brazil.
Faria G; Serviço de Pesquisa, Fundação Hemominas, Belo Horizonte, Minas Gerais, Brazil.
Mendes F; Serviço de Pesquisa, Fundação Hemominas, Belo Horizonte, Minas Gerais, Brazil.
Luizon MR; Programa de Pós-Graduação em Genética, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, Minas Gerais, Brazil.; Departamento de Genética, Ecologia e Evolução, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, Minas Gerais, Brazil.
Viana MB; Faculdade de Medicina/NUPAD, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, Minas Gerais, Brazil.; Pokaż więcej
Źródło :: Annals of hematology [Ann Hematol] 2020 Jul; Vol. 99 (7), pp. 1453-1463. Date of Electronic Publication: 2020 May 23.
Typ publikacji :: Journal Article
Journal Info :: Publisher: Springer Verlag Country of Publication: Germany NLM ID: 9107334 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-0584 (Electronic) Linking ISSN: 09395555 NLM ISO Abbreviation: Ann. Hematol. Subsets: MEDLINE
MeSH Terms :: Genes, myb*
Polymorphism, Single Nucleotide*
Anemia, Sickle Cell/*diagnosis
Anemia, Sickle Cell/*genetics
Fetal Hemoglobin/*metabolism
GTP-Binding Proteins/*genetics
Repressor Proteins/*genetics
Alleles ; Anemia, Sickle Cell/blood ; Anemia, Sickle Cell/epidemiology ; Brazil/epidemiology ; Child ; Child, Preschool ; Cohort Studies ; Female ; Fetal Hemoglobin/genetics ; Genetic Predisposition to Disease ; Genome-Wide Association Study ; Humans ; Infant ; Infant, Newborn ; Male ; Prognosis ; Retrospective Studies
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 15 15.

Tytuł :: De novo leaf transcriptome assembly of Bougainvillea spectabilis for the identification of genes involves in the secondary metabolite pathways.
Autorzy :: Alsamadany H; Department of Biological Sciences, Faculty of Science, King Abdulaziz University, Jeddah, Saudi Arabia. Electronic address: .; Pokaż więcej
Źródło :: Gene [Gene] 2020 Jul 01; Vol. 746, pp. 144660. Date of Electronic Publication: 2020 Apr 08.
Typ publikacji :: Journal Article
Journal Info :: Publisher: Elsevier/North-Holland Country of Publication: Netherlands NLM ID: 7706761 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-0038 (Electronic) Linking ISSN: 03781119 NLM ISO Abbreviation: Gene Subsets: MEDLINE
MeSH Terms :: Gene Expression Profiling*
Plant Leaves*/genetics
Plant Leaves*/metabolism
Polymorphism, Single Nucleotide*
Software*
Gene Expression Regulation, Plant/*physiology
Transcriptome/*physiology
Nyctaginaceae/genetics ; Nyctaginaceae/metabolism
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 16 16.

Tytuł :: Combined effects of AKT serine/threonine kinase 1 polymorphisms and environment on congenital heart disease risk: A case-control study.
Autorzy :: Zhao J; Department of Cardiology.; Department of Cardiology, Chengdu Shang Jin Nan Fu Hospital, West China Hospital, Sichuan University, Chengdu, Sichuan Province, China.
Zeng Z; Department of Cardiology.; Department of Cardiology, Chengdu Shang Jin Nan Fu Hospital, West China Hospital, Sichuan University, Chengdu, Sichuan Province, China.; Pokaż więcej
Źródło :: Medicine [Medicine (Baltimore)] 2020 Jun 26; Vol. 99 (26), pp. e20400.
Typ publikacji :: Journal Article
Journal Info :: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 2985248R Publication Model: Print Cited Medium: Internet ISSN: 1536-5964 (Electronic) Linking ISSN: 00257974 NLM ISO Abbreviation: Medicine (Baltimore) Subsets: Core Clinical (AIM); MEDLINE
MeSH Terms :: Polymorphism, Single Nucleotide*
Heart Defects, Congenital/*genetics
Proto-Oncogene Proteins c-akt/*genetics
Smoking/*adverse effects
Adolescent ; Alleles ; Case-Control Studies ; Child ; Child, Preschool ; China ; Female ; Genetic Predisposition to Disease ; Genotype ; Heterozygote ; Humans ; Male
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 17 17.

Tytuł :: A comprehensive evaluation of single nucleotide polymorphisms associated with osteosarcoma risk: A protocol for systematic review and network meta-analysis.
Autorzy :: Ye ZM; Ruikang School of Clinical Medicine.
Luo MB; Ruikang School of Clinical Medicine.
Zhang C; Graduate School, Guangxi University of Chinese Medicine.
Zheng JH; Department of Cardiology.
Gao HJ; Department of Urinary Surgery, Ruikang Hospital Affiliated to Guangxi University of Chinese Medicine, Nanning, Guangxi.
Tang YM; Department of Gastroenterology, Ruikang Hospital Affiliated to Guangxi University of Chinese Medicine, Nanning, China.; Pokaż więcej
Źródło :: Medicine [Medicine (Baltimore)] 2020 Jun 26; Vol. 99 (26), pp. e20486.
Typ publikacji :: Journal Article
Journal Info :: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 2985248R Publication Model: Print Cited Medium: Internet ISSN: 1536-5964 (Electronic) Linking ISSN: 00257974 NLM ISO Abbreviation: Medicine (Baltimore) Subsets: Core Clinical (AIM); MEDLINE
MeSH Terms :: Polymorphism, Single Nucleotide*
Bone Neoplasms/*genetics
Osteosarcoma/*genetics
Genetic Predisposition to Disease ; Humans ; Network Meta-Analysis ; Research Design ; Risk Assessment ; Systematic Reviews as Topic
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 18 18.

Tytuł :: Interferon-Induced Transmembrane Protein 3 Genetic Variant rs12252-C Associated With Disease Severity in Coronavirus Disease 2019.
Autorzy :: Zhang Y; Beijing Youan Hospital, Capital Medical University, Beijing, People's Republic of China.; Chinese Academy of Medical Science Oxford Institute, University of Oxford, Oxford, United Kingdom.
Qin L; Beijing Youan Hospital, Capital Medical University, Beijing, People's Republic of China.
Zhao Y; Beijing Youan Hospital, Capital Medical University, Beijing, People's Republic of China.
Zhang P; Chinese Academy of Medical Science Oxford Institute, University of Oxford, Oxford, United Kingdom.; Wellcome Centre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
Xu B; Beijing Youan Hospital, Capital Medical University, Beijing, People's Republic of China.
Li K; Beijing Youan Hospital, Capital Medical University, Beijing, People's Republic of China.
Liang L; Beijing Youan Hospital, Capital Medical University, Beijing, People's Republic of China.
Zhang C; Beijing Youan Hospital, Capital Medical University, Beijing, People's Republic of China.
Dai Y; Beijing Youan Hospital, Capital Medical University, Beijing, People's Republic of China.
Feng Y; Beijing Youan Hospital, Capital Medical University, Beijing, People's Republic of China.
Sun J; Beijing Youan Hospital, Capital Medical University, Beijing, People's Republic of China.
Hu Z; Beijing Youan Hospital, Capital Medical University, Beijing, People's Republic of China.
Xiang H; Beijing Youan Hospital, Capital Medical University, Beijing, People's Republic of China.
Knight JC; Chinese Academy of Medical Science Oxford Institute, University of Oxford, Oxford, United Kingdom.; Wellcome Centre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
Dong T; Chinese Academy of Medical Science Oxford Institute, University of Oxford, Oxford, United Kingdom.; MRC Human Immunology Unit, MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, United Kingdom.
Jin R; Beijing Youan Hospital, Capital Medical University, Beijing, People's Republic of China.; Pokaż więcej
Źródło :: The Journal of infectious diseases [J Infect Dis] 2020 Jun 16; Vol. 222 (1), pp. 34-37.
Typ publikacji :: Journal Article
Journal Info :: Publisher: Oxford University Press Country of Publication: United States NLM ID: 0413675 Publication Model: Print Cited Medium: Internet ISSN: 1537-6613 (Electronic) Linking ISSN: 00221899 NLM ISO Abbreviation: J. Infect. Dis. Subsets: Core Clinical (AIM); MEDLINE
MeSH Terms :: Alleles*
Polymorphism, Single Nucleotide*
Severity of Illness Index*
Betacoronavirus/*genetics
Coronavirus Infections/*genetics
Membrane Proteins/*genetics
Pneumonia, Viral/*genetics
RNA-Binding Proteins/*genetics
Adult ; Aged ; Aged, 80 and over ; Cohort Studies ; Coronavirus Infections/virology ; Female ; Genotype ; High-Throughput Nucleotide Sequencing ; Homozygote ; Hospitalization ; Humans ; Male ; Middle Aged ; Pandemics ; Pneumonia, Viral/virology ; Real-Time Polymerase Chain Reaction
SCR Disease Name :: COVID-19
SCR Organism :: severe acute respiratory syndrome coronavirus 2
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 19 19.

Tytuł :: Association between HIF-1α gene polymorphisms and lung cancer: A meta-analysis.
Autorzy :: Xu S; Department of Respiratory Medicine, Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University, Hangzhou.; Department of Respiratory Medicine, Ningbo Medical Center Lihuili Hospital, Ningbo, Zhejiang, China.
Ying K; Department of Respiratory Medicine, Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University, Hangzhou.; Pokaż więcej
Źródło :: Medicine [Medicine (Baltimore)] 2020 Jun 12; Vol. 99 (24), pp. e20610.
Typ publikacji :: Journal Article; Meta-Analysis
Journal Info :: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 2985248R Publication Model: Print Cited Medium: Internet ISSN: 1536-5964 (Electronic) Linking ISSN: 00257974 NLM ISO Abbreviation: Medicine (Baltimore) Subsets: Core Clinical (AIM); MEDLINE
MeSH Terms :: Polymorphism, Single Nucleotide*
Hypoxia-Inducible Factor 1, alpha Subunit/*genetics
Lung Neoplasms/*genetics
Humans ; Lung Neoplasms/epidemiology ; Risk Assessment
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 20 20.

Tytuł :: Human genetics of HCV infection phenotypes in the era of direct-acting antivirals.
Autorzy :: Nahon P; AP-HP, Hôpital Jean Verdier, Liver Unit, Bondy, France.; University Paris 13, Sorbonne Paris Cité, 'équipe labellisée Ligue Contre Le Cancer', Bobigny, France.; Inserm UMR-1162, Functional Genetics of Solid Tumors, Paris, France.
Cobat A; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Necker Hospital for Sick Children, Paris, France. .; Université de Paris, Imagine Institute, Paris, France. .; Pokaż więcej
Źródło :: Human genetics [Hum Genet] 2020 Jun; Vol. 139 (6-7), pp. 855-863. Date of Electronic Publication: 2020 Feb 25.
Typ publikacji :: Journal Article; Review
Journal Info :: Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1203 (Electronic) Linking ISSN: 03406717 NLM ISO Abbreviation: Hum. Genet. Subsets: MEDLINE
MeSH Terms :: Human Genetics*
Polymorphism, Single Nucleotide*
Antiviral Agents/*therapeutic use
Carcinoma, Hepatocellular/*genetics
Hepatitis C, Chronic/*complications
Liver Cirrhosis/*genetics
Liver Neoplasms/*genetics
Carcinoma, Hepatocellular/metabolism ; Carcinoma, Hepatocellular/virology ; Disease Progression ; Genome-Wide Association Study ; Hepacivirus/drug effects ; Hepacivirus/genetics ; Hepatitis C, Chronic/drug therapy ; Hepatitis C, Chronic/genetics ; Hepatitis C, Chronic/virology ; Humans ; Liver Cirrhosis/metabolism ; Liver Cirrhosis/virology ; Liver Neoplasms/metabolism ; Liver Neoplasms/virology ; Phenotype ; Risk Factors
: Czasopismo naukowe

Szczegóły

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