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Wyszukujesz frazę ""Diabetes Mellitus genetics"" wg kryterium: Temat


Tytuł :
Family Phenotypic Heterogeneity Caused by Mitochondrial DNA Mutation A3243G
Autorzy :
Daniela Alves
Maria Eufémia Calmeiro
Carmo Macário
Rosa Silva
Pokaż więcej
Temat :
Child
Deafness/genetics
Diabetes Mellitus/genetics
DNA, Mitochondrial/genetics
Mutation
Medicine
Medicine (General)
R5-920
Źródło :
Acta Médica Portuguesa, Vol 30, Iss 7-8, Pp 581-585 (2017)
Opis pliku :
electronic resource
Relacje :
http://actamedicaportuguesa.com/revista/index.php/amp/article/view/8638; https://doaj.org/toc/0870-399X; https://doaj.org/toc/1646-0758
Dostęp URL :
https://doaj.org/article/9f8f1653d6694d698d3a3f1f1871f8f6
Czasopismo naukowe
Tytuł :
Letter to the Editor: Maternally Inherited Diabetes and Deafness is Not Only Biorgan but Multiorgan
Autorzy :
Josef Finsterer
Sinda Zarrouk-Mahjoub
Pokaż więcej
Temat :
Child
Deafness/genetics
Diabetes Mellitus/genetics
DNA, Mitochondrial/genetics
Mutation
Medicine
Medicine (General)
R5-920
Źródło :
Acta Médica Portuguesa, Vol 30, Iss 9, Pp 665-666 (2017)
Opis pliku :
electronic resource
Relacje :
http://actamedicaportuguesa.com/revista/index.php/amp/article/view/9716; https://doaj.org/toc/0870-399X; https://doaj.org/toc/1646-0758
Dostęp URL :
https://doaj.org/article/72f93549ec384caf87be8a696bb7d332
Czasopismo naukowe
Tytuł :
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
Autorzy :
Teumer, Alexander
Li, Yong
Wuttke, Matthias
Giri, Ayush
Qiu, Chengxiang
Kirsten, Holger
Tin, Adrienne
Feitosa, Mary F.
Chai, Jin-Fang
Cocca, Massimiliano
Gorski, Mathias
Horn, Katrin
Li, Man
Marten, Jonathan
van der Most, Peter J.
Burkhardt, Ralph
Coresh, Josef
de Borst, Martin H.
Ehret, Georg
Endlich, Karlhans
Felix, Janine F.
Franke, Andre
Freedman, Barry I.
Freitag-Wolf, Sandra
Giedraitis, Vilmantas
Grundner-Culemann, Franziska
Gudnason, Vilmundur
Hicks, Andrew A.
Ikram, M. Arfan
Ingelsson, Erik
Jaddoe, Vincent W. V.
Josyula, Navya Shilpa
Khor, Chiea-Chuen
Koenig, Wolfgang
Kovacs, Peter
Kronenberg, Florian
Lindgren, Cecilia M.
Liu, Jianjun
Lyytikäinen, Leo-Pekka
Mahajan, Anubha
Mascalzoni, Deborah
Miliku, Kozeta
Müller-Nurasyid, Martina
Mychaleckyj, Josyf C.
Palmer, Nicholette D.
Poulain, Tanja
Raffield, Laura M.
Rice, Kenneth M.
Rivadeneira, Fernando
Sabanayagam, Charumathi
Smith, Albert V.
Sun, Benjamin B.
Szymczak, Silke
Taylor, Kent D.
Thio, Chris H. L.
Uitterlinden, André G.
van der Harst, Pim
Verweij, Niek
Völker, Uwe
Wang, Chaolong
Yang, Qiong
Devuyst, Olivier
Edwards, Todd L.
Ho, Kevin
Morris, Andrew P.
Pendergrass, Sarah A.
Rotter, Jerome I.
Stefansson, Kari
Susztak, Katalin
Scholz, Markus
Butterworth, Adam S.
Hung, Adriana M.
Pattaro, Cristian
Köttgen, Anna
Ghasemi, Sahar
Prins, Bram P.
Hermle, Tobias
Sieber, Karsten B.
Chu, Audrey Y.
Bansal, Nisha
Wang, Lihua
Fuchsberger, Christian
Hoppmann, Anselm
Noce, Damia
Nutile, Teresa
Sedaghat, Sanaz
Sveinbjornsson, Gardar
Tayo, Bamidele O.
Xu, Yizhe
Yu, Zhi
Gerstner, Lea
Ärnlöv, Johan
Bakker, Stephan J. L.
Baptista, Daniela
Biggs, Mary L.
Boerwinkle, Eric
Brenner, Hermann
Carroll, Robert J.
Chee, Miao-Li
Chee, Miao-Ling
Chen, Mengmeng
Cheng, Ching-Yu
Cook, James P.
Corre, Tanguy
Danesh, John
De Grandi, Alessandro
de Mutsert, Renée
de Vries, Aiko P. J.
Degenhardt, Frauke
Dittrich, Katalin
Divers, Jasmin
Eckardt, Kai-Uwe
Franco, Oscar H.
Gansevoort, Ron T.
Gögele, Martin
Gudbjartsson, Daniel F.
Hamet, Pavel
Harris, Tamara B.
Holm, Hilma
Foo, Valencia Hui Xian
Hwang, Shih-Jen
Jakobsdottir, Johanna
Jung, Bettina
Kähönen, Mika
Kiess, Wieland
Körner, Antje
Kramer, Holly
Krämer, Bernhard K.
Lange, Leslie A.
Langefeld, Carl D.
Lee, Jeannette Jen-Mai
Lehtimäki, Terho
Lieb, Wolfgang
Lim, Su-Chi
Lind, Lars
Loeffler, Markus
Maranville, Joseph C.
McMullen, Barbara
Meisinger, Christa
Meitinger, Thomas
Mook-Kanamori, Dennis O.
Nauck, Matthias
Nikus, Kjell
Ning, Boting
Noordam, Raymond
Connell, Jeffrey O’
Olafsson, Isleifur
Peters, Annette
Podgornaia, Anna I.
Ponte, Belen
Pramstaller, Peter P.
Rabelink, Ton J.
Reilly, Dermot F.
Rettig, Rainer
Rheinberger, Myriam
Runz, Heiko
Ryan, Kathleen A.
Saum, Kai-Uwe
Schöttker, Ben
Shaffer, Christian M.
Shi, Yuan
Strauch, Konstantin
Stumvoll, Michael
Tai, E-Shyong
Tan, Nicholas Y. Q.
Teren, Andrej
Tham, Yih-Chung
Thiery, Joachim
Thomsen, Hauke
Thorsteinsdottir, Unnur
Tönjes, Anke
Tremblay, Johanne
Vogelezang, Suzanne
Waldenberger, Melanie
Wilson, Otis D.
Wong, Charlene
Wong, Tien-Yin
Yasuda, Masayuki
Akilesh, Shreeram
Bochud, Murielle
Böger, Carsten A.
Parsa, Afshin
Psaty, Bruce M.
Wilson, James G.
Snieder, Harold
Heid, Iris M.
Pokaż więcej
Temat :
610 Medicine & health
Drosophila melanogaster/genetics
Genetic Loci
360 Social problems & social services
Animals
Risk Factors
Creatinine/urine
Meta-Analysis as Topic
Albuminuria/genetics
Article
Gene Expression Regulation
Medical Genetics
Medicinsk genetik
Chromosome Mapping
Kidney diseases
Genome-Wide Association Study
Science
Genetic Predisposition to Disease
Humans
Genome-wide association studies
Diabetes Mellitus/genetics
Phenomics
Źródło :
Nature Communications, Vol 10, Iss 1, Pp 1-19 (2019)
Teumer, Alexander; Li, Yong; Ghasemi, Sahar; Prins, Bram P; Wuttke, Matthias; Hermle, Tobias; Giri, Ayush; Sieber, Karsten B; Qiu, Chengxiang; Kirsten, Holger; Tin, Adrienne; Chu, Audrey Y; Bansal, Nisha; Feitosa, Mary F; Wang, Lihua; Chai, Jin-Fang; Cocca, Massimiliano; Fuchsberger, Christian; Gorski, Mathias; Hoppmann, Anselm; ... (2019). Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria. Nature communications, 10(1), p. 4130. Nature Publishing Group 10.1038/s41467-019-11576-0
Teumer, A, Li, Y, Ghasemi, S, Prins, B P, Wuttke, M, Hermle, T, Giri, A, Sieber, K B, Qiu, C, Kirsten, H, Tin, A, Chu, A Y, Bansal, N, Feitosa, M F, Wang, L, Chai, J-F, Cocca, M, Fuchsberger, C, Gorski, M, Hoppmann, A, Horn, K, Li, M, Marten, J, Noce, D, Nutile, T, Sedaghat, S, Sveinbjornsson, G, Tayo, B O, van der Most, P J, Xu, Y, Yu, Z, Gerstner, L, Ärnlöv, J, Bakker, S J L, Baptista, D, Biggs, M L, Boerwinkle, E, Brenner, H, Burkhardt, R, Carroll, R J, Chee, M-L, Chee, M-L, Chen, M, Cheng, C-Y, Cook, J P, Coresh, J, Corre, T, Danesh, J, de Borst, M H, De Grandi, A, de Mutsert, R, de Vries, A P J, Degenhardt, F, Dittrich, K, Divers, J, Eckardt, K-U, Ehret, G, Endlich, K, Felix, J F, Franco, O H, Franke, A, Freedman, B I, Freitag-Wolf, S, Gansevoort, R T, Giedraitis, V, Gögele, M, Grundner-Culemann, F, Gudbjartsson, D F, Gudnason, V, Hamet, P, Harris, T B, Hicks, A A, Holm, H, Foo, V H X, Hwang, S-J, Ikram, M A, Ingelsson, E, Jaddoe, V W V, Jakobsdottir, J, Josyula, N S, Jung, B, Kähönen, M, Khor, C-C, Kiess, W, Koenig, W, Körner, A, Kovacs, P, Kramer, H, Krämer, B K, Kronenberg, F, Lange, L A, Langefeld, C D, Lee, J J-M, Lehtimäki, T, Lieb, W, Lim, S-C, Lind, L, Lindgren, C M, Liu, J, Loeffler, M, Lyytikäinen, L-P, Mahajan, A, Maranville, J C, Mascalzoni, D, McMullen, B, Meisinger, C, Meitinger, T, Miliku, K, Mook-Kanamori, D O, Müller-Nurasyid, M, Mychaleckyj, J C, Nauck, M, Nikus, K, Ning, B, Noordam, R, Connell, J O, Olafsson, I, Palmer, N D, Peters, A, Podgornaia, A I, Ponte, B, Poulain, T, Pramstaller, P P, Rabelink, T J, Raffield, L M, Reilly, D F, Rettig, R, Rheinberger, M, Rice, K M, Rivadeneira, F, Runz, H, Ryan, K A, Sabanayagam, C, Saum, K-U, Schöttker, B, Shaffer, C M, Shi, Y, Smith, A V, Strauch, K, Stumvoll, M, Sun, B B, Szymczak, S, Tai, E-S, Tan, N Y Q, Taylor, K D, Teren, A, Tham, Y-C, Thiery, J, Thio, C H L, Thomsen, H, Thorsteinsdottir, U, Tönjes, A, Tremblay, J, Uitterlinden, A G, van der Harst, P, Verweij, N, Vogelezang, S, Völker, U, Waldenberger, M, Wang, C, Wilson, O D, Wong, C, Wong, T-Y, Yang, Q, Yasuda, M, Akilesh, S, Bochud, M, Böger, C A, Devuyst, O, Edwards, T L, Ho, K, Morris, A P, Parsa, A, Pendergrass, S A, Psaty, B M, Rotter, J I, Stefansson, K, Wilson, J G, Susztak, K, Snieder, H, Heid, I M, Scholz, M, Butterworth, A S, Hung, A M, Pattaro, C & Köttgen, A 2019, ' Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria ', Nature Communications, vol. 10, no. 1, pp. 4130 . https://doi.org/10.1038/s41467-019-11576-0
Opis pliku :
application/pdf
Tytuł :
Asociación de variantes en genes de las proteínas desacoplantes con diabetes mellitus tipo 2 en una población del nordeste colombiano
Autorzy :
Liliana Franco-Hincapié
Constanza Elena Duque
María Victoria Parra
Natalia Gallego
Alberto Villegas
Andrés Ruiz-Linares
Gabriel Bedoya
Pokaż więcej
Temat :
Diabetes mellitus/genetics
insulin resistance
obesity
polymorphism
genotype
haplotypes
Medicine
Arctic medicine. Tropical medicine
RC955-962
Źródło :
Biomédica: revista del Instituto Nacional de Salud, Vol 29, Iss 1, Pp 108-118 (2009)
Opis pliku :
electronic resource
Relacje :
http://www.revistabiomedica.org/index.php/biomedica/article/view/46; https://doaj.org/toc/0120-4157
Dostęp URL :
https://doaj.org/article/1437abf5cc6a482da733f55baa680f72
Czasopismo naukowe
Tytuł :
Calcineurin Inhibitors Downregulate HNF-1 and May Affect the Outcome of HNF1B Patients After Renal Transplantation
Autorzy :
Faguer, Stanislas
Esposito, Laure
Casemayou, Audrey
Pirson, Yves
Decramer, Stephane
Cartery, Claire
Hazzan, Marc
Garrigue, Valerie
Roussey, Gwenaelle
Cointault, Olivier
Ho, Thien
Merville, Pierre
Devuyst, Olivier
Gourdy, Pierre
Chassaing, Nicolas
Bascands, Jean-Loup
Kamar, Nassim
Schanstra, Joost-Peter
Rostaing, Lionel
Chauveau, Dominique
Pokaż więcej
Temat :
Mesh:Cross-Sectional Studies
Mesh:Kidney Failure
Mesh:Chronic/genetics
Mesh:Genetic Predisposition to Disease
Mesh:Time Factors
Mesh:Treatment Outcome
Mesh:NFATC Transcription Factors/genetics
Mesh:RNA Interference
Mesh:Liver/drug effects
Mesh:Adult
Mesh:Calcineurin Inhibitors/adverse effects
Mesh:Dose-Response Relationship
Mesh:Drug
Mesh:Immunosuppressive Agents/adverse effects
Mesh:Infant
Mesh:Newborn
Mesh:Kidney/metabolism
Mesh:Chronic/diagnosis
Mesh:Chronic/metabolism
Mesh:Chronic/surgery
Mesh:Kidney Transplantation*/adverse effects
Mesh:Liver/metabolism
Mesh:Liver/pathology
Mesh:Mutation
Mesh:NFATC Transcription Factors/metabolism
Mesh:Pancreas Transplantation
Mesh:Phenotype
Mesh:Retrospective Studies
Mesh:Transfection
Mesh:Kidney/pathology
Mesh:Adolescent
Mesh:Chemical and Drug Induced Liver Injury/etiology
Mesh:Chemical and Drug Induced Liver Injury/genetics
Mesh:Chemical and Drug Induced Liver Injury/metabolism
Mesh:Child
Mesh:Kidney/drug effects
Mesh:Hepatocyte Nuclear Factor 1-beta/genetics
Mesh:Diabetes Mellitus/chemically induced
Mesh:Diabetes Mellitus/metabolism
Mesh:Down-Regulation
Mesh:Preschool
Mesh:Diabetes Mellitus/genetics
Mesh:France
Mesh:Hep G2 Cells
Mesh:Humans
Mesh:Hepatocyte Nuclear Factor 1-beta/metabolism
Sciences du Vivant [q-bio]

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