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1دورية أكاديمية
المؤلفون: Hamano S., Nishibori Y., Hada I., Mikami N., Ito-Nitta N., Fukuhara D., Kudo A., Xiao Z., Nukui M., Patrakka J., Tryggvason K., Yan K.
المساهمون: DUKE-NUS MEDICAL SCHOOL
المصدر: Unpaywall 20191101
مصطلحات موضوعية: mammalian target of rapamycin complex 1, tyrosine, carrier protein, CRB2 protein, human, mouse, membrane protein, adult, animal cell, animal experiment, Article, cell maturation, cell membrane, confocal microscopy, controlled study, CRB2 gene, energy, enzyme activation, gene, gene function, genetic association, HEK293 cell line, male, MDCK cell line, newborn, nonhuman, podocyte, protein assembly, protein glycosylation, protein localization
العلاقة: Hamano S., Nishibori Y., Hada I., Mikami N., Ito-Nitta N., Fukuhara D., Kudo A., Xiao Z., Nukui M., Patrakka J., Tryggvason K., Yan K. (2018). Association of crumbs homolog-2 with mTORC1 in developing podocyte. PLoS ONE 13 (8) : e0202400. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0202400Test; https://scholarbank.nus.edu.sg/handle/10635/161217Test
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2دورية أكاديمية
المؤلفون: Morchang A., Lee R.C.H., Yenchitsomanus P.-T., Sreekanth G.P., Noisakran S., Chu J.J.H., Limjindaporn T.
المساهمون: MICROBIOLOGY AND IMMUNOLOGY
المصدر: Unpaywall 20191101
مصطلحات موضوعية: abc 294649, caspase 3, caspase 8, caspase 9, phosphotransferase inhibitor, small interfering RNA, sphingosine kinase 2, tumor necrosis factor, tumor necrosis factor superfamily member 12, unclassified drug, phosphotransferase, human, apoptosis, Article, Dengue virus, enzyme activity, gene function, gene silencing, genetic screening, Hep-G2 cell line, Huh-7 cell line, human cell, liver cell, RNA interference, SPHK2 gene, TNFSF12 gene, cell line, genetics, liver, metabolism
العلاقة: Morchang A., Lee R.C.H., Yenchitsomanus P.-T., Sreekanth G.P., Noisakran S., Chu J.J.H., Limjindaporn T. (2017). RNAi screen reveals a role of SPHK2 in dengue virus–mediated apoptosis in hepatic cell lines. PLoS ONE 12 (11) : e0188121. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0188121Test; https://scholarbank.nus.edu.sg/handle/10635/161167Test
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3دورية أكاديمية
المؤلفون: Esslinger U., Garnier S., Korniat A., Proust C., Kararigas G., Müller-Nurasyid M., Empana J.-P., Morley M.P., Perret C., Stark K., Bick A.G., Prasad S.K., Kriebel J., Li J., Tiret L., Strauch K., O'Regan D.P., Marguiles K.B., Seidman J.G., Boutouyrie P., Lacolley P., Jouven X., Hengstenberg C., Komajda M., Hakonarson H., Isnard R., Arbustini E., Grallert H., Cook S.A., Seidman C.E., Regitz-Zagrosek V., Cappola T.P., Charron P., Cambien F., Villard E.
المساهمون: DUKE-NUS MEDICAL SCHOOL
المصدر: Unpaywall 20191101
مصطلحات موضوعية: ALPK3 gene, Article, BAG3 gene, computer model, congestive cardiomyopathy, controlled study, exome, female, FHOD3 gene, FLNC gene, gene, gene expression, gene function, gene identification, gene locus, gene mapping, gene mutation, genetic susceptibility, genome-wide association study, genotype, HSPB7 gene, human, human cell, human tissue, major clinical study, male, missense mutation, MLIP gene, population research, single nucleotide polymorphism
العلاقة: Esslinger U., Garnier S., Korniat A., Proust C., Kararigas G., Müller-Nurasyid M., Empana J.-P., Morley M.P., Perret C., Stark K., Bick A.G., Prasad S.K., Kriebel J., Li J., Tiret L., Strauch K., O'Regan D.P., Marguiles K.B., Seidman J.G., Boutouyrie P., Lacolley P., Jouven X., Hengstenberg C., Komajda M., Hakonarson H., Isnard R., Arbustini E., Grallert H., Cook S.A., Seidman C.E., Regitz-Zagrosek V., Cappola T.P., Charron P., Cambien F., Villard E. (2017). Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy. PLoS ONE 12 (3) : e0172995. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0172995Test; https://scholarbank.nus.edu.sg/handle/10635/161526Test
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4دورية أكاديمية
المؤلفون: Scolnick J.A., Dimon M., Wang I.-C., Huelga S.C., Amorese D.A.
المساهمون: PHYSIOLOGY
المصدر: Unpaywall 20191101
مصطلحات موضوعية: RNA, Article, controlled study, exon, formalin fixed paraffin embedded, frozen section, gene function, gene fusion, gene identification, gene targeting, human, human cell, human tissue, investigative procedures, molecular dynamics, RNA sequence, sequence analysis, tissue section, breast tumor, fluorescence in situ hybridization, genetics, high throughput sequencing, Paget nipple disease, pathology, Breast Neoplasms, Carcinoma, Ductal, Breast, High-Throughput Nucleotide Sequencing, Humans
العلاقة: Scolnick J.A., Dimon M., Wang I.-C., Huelga S.C., Amorese D.A. (2015). An efficient method for identifying gene fusions by targeted RNA sequencing from fresh frozen and FFPE samples. PLoS ONE 10 (7) : e0128916. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0128916Test; https://scholarbank.nus.edu.sg/handle/10635/161501Test
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5دورية أكاديمية
المؤلفون: Narang V., Ramli M.A., Singhal A., Kumar P., de Libero G., Poidinger M., Monterola C.
المساهمون: BIOLOGY (NU)
المصدر: Unpaywall 20191101
مصطلحات موضوعية: Article, autoanalysis, data analysis, gene function, gene identification, gene regulatory network, gene targeting, genetic algorithm, human genetics, mathematical analysis, MCF 7 cell line, microarray analysis, molecular evolution, transcription regulation, algorithm, biology, breast tumor, classification, female, gene expression profiling, genetic database, genetics, human, metabolism, procedures, tumor cell line, estrogen, tumor marker, Algorithms, Biomarkers
العلاقة: Narang V., Ramli M.A., Singhal A., Kumar P., de Libero G., Poidinger M., Monterola C. (2015). Automated Identification of Core Regulatory Genes in Human Gene Regulatory Networks. PLoS Computational Biology 11 (9) : e1004504. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pcbi.1004504Test; https://scholarbank.nus.edu.sg/handle/10635/161933Test
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6دورية أكاديمية
المؤلفون: Todesco M., Kim S.-T., Chae E., Bomblies K., Zaidem M., Smith L.M., Weigel D., Laitinen R.A.E.
المساهمون: BIOLOGICAL SCIENCES
المصدر: Unpaywall 20191101
مصطلحات موضوعية: genomic DNA, plant DNA, ACD6 protein, Arabidopsis, ankyrin, Arabidopsis protein, ACD6 gene, allele, Arabidopsis thaliana, article, autoimmunity, cell death, epistasis, evolutionary adaptation, gene function, gene interaction, gene locus, gene mapping, gene sequence, genetic variability, haplotype, immunoregulation, immunostimulation, nonhuman, nucleotide sequence, plant cell, plant defense, plant gene, plant immunity, plant pathogen interaction
العلاقة: Todesco M., Kim S.-T., Chae E., Bomblies K., Zaidem M., Smith L.M., Weigel D., Laitinen R.A.E. (2014). Activation of the Arabidopsis thaliana Immune System by Combinations of Common ACD6 Alleles. PLoS Genetics 10 (7) : e1004459. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pgen.1004459Test; https://scholarbank.nus.edu.sg/handle/10635/161949Test
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7دورية أكاديمية
المؤلفون: Liu H., Li Y., Hung K.K.H., Wang N., Wang C., Chen X., Sheng D., Fu X., See K., Foo J.N., Low H., Liany H., Irwan I.D., Liu J., Yang B., Chen M., Yu Y., Yu G., Niu G., You J., Zhou Y., Ma S., Wang T., Yan X., Goh B.K., Common J.E.A., Lane B.E., Sun Y., Zhou G., Lu X., Wang Z., Tian H., Cao Y., Chen S., Liu Q., Zhang F.
المساهمون: PATHOLOGY
المصدر: Unpaywall 20191101
مصطلحات موضوعية: ABCB6 gene, animal experiment, article, Chinese, clinical article, coloboma, controlled study, dyschromatosis universalis hereditaria, embryo, exome, gene, gene expression regulation, gene function, gene mutation, gene sequence, genetic analysis, genetic association, genetic disorder, genetic linkage, genome analysis, human, human cell, immunohistochemistry, melanocyte, mutational analysis, nonhuman, nucleotide sequence, phenotype, real time polymerase chain reaction, sequence analysis
العلاقة: Liu H., Li Y., Hung K.K.H., Wang N., Wang C., Chen X., Sheng D., Fu X., See K., Foo J.N., Low H., Liany H., Irwan I.D., Liu J., Yang B., Chen M., Yu Y., Yu G., Niu G., You J., Zhou Y., Ma S., Wang T., Yan X., Goh B.K., Common J.E.A., Lane B.E., Sun Y., Zhou G., Lu X., Wang Z., Tian H., Cao Y., Chen S., Liu Q., Liu J., Zhang F. (2014). Genome-wide linkage, exome sequencing and functional analyses identify ABCB6 as the pathogenic gene of dyschromatosis universalis hereditaria. PLoS ONE 9 (2) : e87250. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0087250Test; https://scholarbank.nus.edu.sg/handle/10635/161431Test
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8دورية أكاديمية
المؤلفون: Khan S., Greco D., Michailidou K., Milne R.L., Muranen T.A., Heikkinen T., Aaltonen K., Dennis J., Bolla M.K., Liu J., Hall P., Irwanto A., Humphreys K., Li J., Czene K., Chang-Claude J., Hein R., Rudolph A., Seibold P., Flesch-Janys D., Fletcher O., Peto J., Silva I.D.S., Johnson N., Gibson L., Aitken Z., Hopper J.L., Tsimiklis H., Bui M., Makalic E., Schmidt D.F., Southey M.C., Apicella C., Stone J., Waisfisz Q., Meijers-Heijboer H., Adank M.A., Van Der Luijt R.B., Meindl A., Schmutzler R.K., Müller-Myhsok B., Lichtner P., Turnbull C., Rahman N., Chanock S.J., Hunter D.J., Cox A., Cross S.S., Reed M.W.R., Schmidt M.K., Broeks A., Van'T Veer L.J., Hogervorst F.B., Fasching P.A., Schrauder M.G., Ekici A.B., Beckmann M.W., Bojesen S.E., Nordestgaard B.G., Nielsen S.F., Flyger H., Benitez J., Zamora P.M., Perez J.I.A., Haiman C.A., Henderson B.E., Schumacher F., March L.L., Pharoah P.D.P., Dunning A.M., Shah M., Luben R., Brown J., Couch F.J., Wang X., Vachon C., Olson J.E., Lambrechts D., Moisse M., Paridaens R., Christiaens M.-R., Guénel P., Truong T., Laurent-Puig P., Mulot C., Marme F., Burwinkel B., Schneeweiss A., Sohn C., Sawyer E.J., Tomlinson I., Kerin M.J., Miller N., Andrulis I.L., Knight J.A., Tchatchou S., Mulligan A.M., Dörk T., Bogdanova N.V., Antonenkova N.N., Anton-Culver H., Darabi H., Eriksson M., Garcia-Closas M., Figueroa J., Lissowska J., Brinton L., Devilee P., Tollenaar R.A.E.M., Seynaeve C., Van Asperen C.J., Kristensen V.N., Australian Ovarian Cancer Study Group S.S., Tol A.E., Ambrosone C.B., Yannoukakos D., Lindblom A., Margolin S., Radice P., Peterlongo P., Barile M., Mariani P., Hooning M.J., Martens J.W.M., Margriet Collée J., Jager A., Jakubowska A., Lubinski J., Jaworska-Bieniek K., Durda K., Giles G.G., McLean C., Brauch H., Brüning T., Ko Y.-D., The Genica Network H.B., Dieffenbach A.K., Arndt V., Stegmaier C., Swerdlow A., Ashworth A., Orr N., Jones M., Simard J., Goldberg M.S., Labrèche F., Dumont M., Winqvist R., Pylkäs K., Jukkola-Vuorinen A., Grip M., Kataja V., Kosma V.-M., Hartikainen J.M., Mannermaa A., Hamann U., Chenevix-Trench G., Blomqvist C., Aittomäki K., Easton D.F., Nevanlinna H.
المساهمون: DEPT OF SURGERY
المصدر: Unpaywall 20191101
مصطلحات موضوعية: caspase 8, microRNA, 3' untranslated region, estrogen receptor, adult, allele, apoptosis, Article, binding site, breast cancer, cancer risk, cancer susceptibility, CASP8 gene, controlled study, disease association, DROSHA gene, estrogen receptor positive breast cancer, ethnic group, female, gene, gene expression regulation, gene function, genetic association, genotype, HDDC3 gene, human, major clinical study, MUSTN1 gene, MYCL1 gene, RNA processing
العلاقة: Khan S., Greco D., Michailidou K., Milne R.L., Muranen T.A., Heikkinen T., Aaltonen K., Dennis J., Bolla M.K., Liu J., Hall P., Irwanto A., Humphreys K., Li J., Czene K., Chang-Claude J., Hein R., Rudolph A., Seibold P., Flesch-Janys D., Fletcher O., Peto J., Silva I.D.S., Johnson N., Gibson L., Aitken Z., Hopper J.L., Tsimiklis H., Bui M., Makalic E., Schmidt D.F., Southey M.C., Apicella C., Stone J., Waisfisz Q., Meijers-Heijboer H., Adank M.A., Van Der Luijt R.B., Meindl A., Schmutzler R.K., Müller-Myhsok B., Lichtner P., Turnbull C., Rahman N., Chanock S.J., Hunter D.J., Cox A., Cross S.S., Reed M.W.R., Schmidt M.K., Broeks A., Van'T Veer L.J., Hogervorst F.B., Fasching P.A., Schrauder M.G., Ekici A.B., Beckmann M.W., Bojesen S.E., Nordestgaard B.G., Nielsen S.F., Flyger H., Benitez J., Zamora P.M., Perez J.I.A., Haiman C.A., Henderson B.E., Schumacher F., March L.L., Pharoah P.D.P., Dunning A.M., Shah M., Luben R., Brown J., Couch F.J., Wang X., Vachon C., Olson J.E., Lambrechts D., Moisse M., Paridaens R., Christiaens M.-R., Guénel P., Truong T., Laurent-Puig P., Mulot C., Marme F., Burwinkel B., Schneeweiss A., Sohn C., Sawyer E.J., Tomlinson I., Kerin M.J., Miller N., Andrulis I.L., Knight J.A., Tchatchou S., Mulligan A.M., Dörk T., Bogdanova N.V., Antonenkova N.N., Anton-Culver H., Darabi H., Eriksson M., Garcia-Closas M., Figueroa J., Lissowska J., Brinton L., Devilee P., Tollenaar R.A.E.M., Seynaeve C., Van Asperen C.J., Kristensen V.N., Australian Ovarian Cancer Study Group S.S., Tol A.E., Ambrosone C.B., Yannoukakos D., Lindblom A., Margolin S., Radice P., Peterlongo P., Barile M., Mariani P., Hooning M.J., Martens J.W.M., Margriet Collée J., Jager A., Jakubowska A., Lubinski J., Jaworska-Bieniek K., Durda K., Giles G.G., McLean C., Brauch H., Brüning T., Ko Y.-D., The Genica Network H.B., Dieffenbach A.K., Arndt V., Stegmaier C., Swerdlow A., Ashworth A., Orr N., Jones M., Simard J., Goldberg M.S., Labrèche F., Dumont M., Winqvist R., Pylkäs K., Jukkola-Vuorinen A., Grip M., Kataja V., Kosma V.-M., Hartikainen J.M., Mannermaa A., Hamann U., Chenevix-Trench G., Blomqvist C., Aittomäki K., Easton D.F., Nevanlinna H. (2014). MicroRNA related polymorphisms and breast cancer risk. PLoS ONE 9 (11) : e109973. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0109973Test; https://scholarbank.nus.edu.sg/handle/10635/161759Test
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9دورية أكاديمية
المؤلفون: Yamanaka Y., Oshima T., Ishihama A., Yamamoto K.
المساهمون: MECHANOBIOLOGY INSTITUTE
المصدر: Unpaywall 20191101
مصطلحات موضوعية: antiporter, bacterial protein, transcription factor, transcription factor DctR, transcription factor GadE, transcription factor GadW, transcription factor NhaR, unclassified drug, Escherichia coli protein, glutamic acid, YdeO protein, E coli, anaerobic respiration, Article, bacterial gene, bacterial genome, bacterial metabolism, binding site, breathing, cellular stress response, chromatin immunoprecipitation, DNA footprinting, Escherichia coli, gel mobility shift assay, gene function, gene identification, genetic regulation, in vivo study, luciferase assay, metabolic regulation
العلاقة: Yamanaka Y., Oshima T., Ishihama A., Yamamoto K. (2014). Characterization of the YdeO regulon in Escherichia coli. PLoS ONE 9 (11) : e111962. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0111962Test; https://scholarbank.nus.edu.sg/handle/10635/161760Test
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10دورية أكاديمية
المؤلفون: Bis J.C., DeStefano A., Liu X., Brody J.A., Choi S.H., Verhaaren B.F.J., Debette S., Ikram M.A., Shahar E., Butler Jr. K.R., Gottesman R.F., Muzny D., Kovar C.L., Psaty B.M., Hofman A., Lumley T., Gupta M., Wolf P.A., Van Duijn C., Gibbs R.A., Mosley T.H., Longstreth Jr. W.T., Boerwinkle E., Seshadri S., Fornage M.
المساهمون: DUKE-NUS MEDICAL SCHOOL
المصدر: Unpaywall 20191101
مصطلحات موضوعية: adult, aged, article, atherosclerosis, brain ischemia, cardiovascular disease, controlled study, female, gene frequency, gene function, gene locus, gene mapping, gene sequence, genetic association, genetic heterogeneity, genetic variability, human, incidence, intron, major clinical study, male, medical research, middle aged, NINJ2 gene, risk assessment, Caucasian, DNA sequence, genetic association study, genetics, ischemia
العلاقة: Bis J.C., DeStefano A., Liu X., Brody J.A., Choi S.H., Verhaaren B.F.J., Debette S., Ikram M.A., Shahar E., Butler Jr. K.R., Gottesman R.F., Muzny D., Kovar C.L., Psaty B.M., Hofman A., Lumley T., Gupta M., Wolf P.A., Van Duijn C., Gibbs R.A., Mosley T.H., Longstreth Jr. W.T., Boerwinkle E., Seshadri S., Fornage M. (2014). Associations of NINJ2 sequence variants with incident ischemic stroke in the Cohorts for Heart and Aging in Genomic Epidemiology (CHARGE) consortium. PLoS ONE 9 (6) : e99798. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0099798Test; https://scholarbank.nus.edu.sg/handle/10635/161403Test
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