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Wyszukujesz frazę ""RNA-Binding Proteins genetics"" wg kryterium: Temat


Tytuł :
TbUTP10, a protein involved in early stages of pre-18S rRNA processing in Trypanosoma brucei
Autorzy :
Faktorová, Drahomíra
Bär, Anita
Hashimi, Hassan
McKenney, Katherine
Horák, Aleš
Schnaufer, Achim
Rubio, Mary Anne T
Alfonzo, Juan D
Lukeš, Julius
Pokaż więcej
Temat :
Gene Silencing
Genes, Essential
Protozoan Proteins/genetics
RNA Processing, Post-Transcriptional
RNA, Ribosomal, 18S/metabolism
RNA, Small Nucleolar/metabolism
RNA-Binding Proteins/genetics
Trypanosoma brucei brucei/enzymology
Źródło :
Faktorová, D, Bär, A, Hashimi, H, McKenney, K, Horák, A, Schnaufer, A, Rubio, M A T, Alfonzo, J D & Lukeš, J 2018, ' TbUTP10, a protein involved in early stages of pre-18S rRNA processing in Trypanosoma brucei ', Molecular and Biochemical Parasitology, vol. 225, pp. 84-93 . https://doi.org/10.1016/j.molbiopara.2018.09.003
Opis pliku :
application/pdf
Tytuł :
Distinct patterns of brain atrophy in Genetic Frontotemporal Dementia Initiative (GENFI) cohort revealed by visual rating scales
Autorzy :
Fumagalli, Giorgio G
Arighi, Andrea
Bocchetta, Martina
Rowe, James
Tagliavini, Fabrizio
Laforce, Robert
Basilico, Paola
Dick, Katrina M
Cash, David M
Harding, Sophie
Mercurio, Matteo
Fenoglio, Chiara
Pietroboni, Anna M
Ghezzi, Laura
Van Swieten, John
Borroni, Barbara
De Mendonça, Alexandre
Masellis, Mario
Tartaglia, Maria C
Graff, Caroline
Frisoni, Giovanni B
Finger, Elizabeth
Sorbi, Sandro
Scarpini, Elio
Rohrer, Jonathan D
Galimberti, Daniela
Genetic FTD Initiative (GENFI)
Pokaż więcej
Temat :
Magnetic Resonance Imaging
Neurology. Diseases of the nervous system
Genetic FTD Initiative (GENFI)
tau Proteins
Brain/diagnostic imaging/pathology
Frontotemporal dementia
International Cooperation
Tau Proteins/genetics
Research
Frontotemporal Dementia/complications/diagnostic imaging/genetics
RNA-Binding Proteins
Genetics
RNA-Binding Proteins/genetics
Progranulins
Female
ddc:618.97
Neurosciences. Biological psychiatry. Neuropsychiatry
MRI
Visual rating
Atrophy/classification/diagnostic imaging/etiology
RC321-571
RC346-429
Progranulins/genetics
Middle Aged
Brain
Nonparametric
Severity of Illness Index
Cohort Studies
Atrophy
Statistics, Nonparametric
Adult
Settore MED/26 - Neurologia
Humans
Male
Statistics
Źródło :
Alzheimer's Research & Therapy
Alzheimer’s Research & Therapy, Vol 10, Iss 1, Pp 1-9 (2018)
Alzheimer's Research and Therapy, Vol. 10, No 1 (2018) P. 46
Opis pliku :
Electronic; application/pdf
Tytuł :
Bayesian association scan reveals loci associated with human lifespan and linked biomarkers.
Autorzy :
McDaid, Aaron F.
Joshi, Peter K.
Komljenovic, Andrea
Deplancke, Bart
Wilson, James F.
Porcu, Eleonora
Li, Hao
Sorrentino, Vincenzo
Litovchenko, Maria
Bevers, Roel P. J.
Rüeger, Sina
Reymond, Alexandre
Bochud, Murielle
Williams, Robert W.
Robinson-Rechavi, Marc
Paccaud, Fred
Rousson, Valentin
Auwerx, Johan
Kutalik, Zoltán
Pokaż więcej
Temat :
Aged
Aged, 80 and over
Arylsulfotransferase/genetics
Bayes Theorem
Biomarkers/analysis
Disease/genetics
European Continental Ancestry Group/genetics
Female
Genome-Wide Association Study
Humans
Longevity/genetics
Male
Nerve Tissue Proteins/genetics
Polymorphism, Single Nucleotide
RNA-Binding Proteins/genetics
Receptors, Nicotinic/genetics
United Kingdom
Article
Źródło :
Nature communications, vol. 8, pp. 15842
McDaid, A F, Joshi, P, Porcu, E, Komljenovic, A, Li, H, Sorrentino, V, Litovchenko, M, Bevers, R, Rüeger, S, Reymond, A, Bochud, M, Deplancke, B, Williams, R, Robinson-Rechavi, M, Paccaud, F, Rousson, V, Auwerx, J, Wilson, J & Kutalik, Z 2017, ' Bayesian association scan reveals loci associated with human lifespan and linked biomarkers ', Nature Communications . https://doi.org/10.1038/ncomms15842
Opis pliku :
application/pdf
Tytuł :
Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder
Autorzy :
Lescai, F
Li, Q
Nyegaard, M
Grove, J
Eickhardt, E
Als, T D
Andorsdottir, G
Biskopstø, M
Hedemand, A
Fiorentino, A
O'Brien, N
Jarram, A
Liang, J
Pallesen, J
Mattheisen, M
Bolund, L
Demontis, D
Wang, A G
McQuillin, A
Mors, O
Wang, J
Børglum, A D
Pokaż więcej
Temat :
Phosphatidylinositol 3-Kinases/genetics
United Kingdom
Polymorphism, Genetic
Research Support, Non-U.S. Gov't
Original Article
Denmark
Gene Regulatory Networks
Bipolar Disorder/genetics
Mutation, Missense
Sequence Analysis, DNA
RNA-Binding Proteins/genetics
Nitric Oxide Synthase Type I/genetics
Journal Article
Calcium-Binding Proteins/genetics
Genetic Predisposition to Disease
Humans
Membrane Proteins/genetics
Phosphoproteins/genetics
Case-Control Studies
Źródło :
Translational Psychiatry, 7 (2), Article e1034. (2017)
Lescai, F, Als, T D, Li, Q, Nyegaard, M, Andorsdottir, G, Biskopstø, M, Hedemand, A, Fiorentino, A, O'Brien, N L, Jarram, A, Liang, T J, Grove, J, Pallesen, J, Eickhardt, E, Mattheisen, M, Bolund, L, Demontis, D, Wang, A G, McQuillin, A, Mors, O, Wang, J & Børglum, A D 2017, ' Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder ', Translational Psychiatry, vol. 7, no. 2, pp. e1034 . https://doi.org/10.1038/tp.2017.3
Lescai, F, Als, T D, Li, Q, Nyegaard, M, Andorsdottir, G, Biskopstø, M, Hedemand, A, Fiorentino, A, O'Brien, N, Jarram, A, Liang, J, Grove, J, Pallesen, J, Eickhardt, E, Mattheisen, M, Bolund, L, Demontis, D, Wang, A G, McQuillin, A, Mors, O, Wang, J & Børglum, A D 2017, ' Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder ', Translational Psychiatry, vol. 7, e1034 . https://doi.org/10.1038/tp.2017.3
Opis pliku :
text; application/pdf
Tytuł :
A mutation in the glutamate-rich region of RNA-binding motif protein 20 causes dilated cardiomyopathy through missplicing of titin and impaired Frank-Starling mechanism
Autorzy :
Beqqali, Abdelaziz
Bollen, I. A. E.
Rasmussen, T. B.
van den Hoogenhof, M. M.
van Deutekom, H. W. M.
Schafer-Korting, M.
Haas, J
Meder, Benjamin
Sorensen, K. E.
van Oort, R. J.
Mogensen, Jens
Hubner, N.
Creemers, E. E.
van der Velden, J.
Pinto, Yigal M
Pokaż więcej
Temat :
Sarcomere Cardiomyopathy Dilated cardiomyopathy Heart failure Alternative splicing RBM20 length-dependent activation calcium homeostasis troponin-i rbm20 expression gene myocardium stiffness reveals tension Cardiovascular System & Cardiology
Heart failure
Alternative splicing
Dilated cardiomyopathy
Cardiomyopathy
RBM20
Sarcomere
Myocytes, Cardiac/metabolism
Phosphorylation
Alternative Splicing
Cyclic AMP-Dependent Protein Kinases/metabolism
Humans
Male
RNA-Binding Proteins/genetics
Case-Control Studies
Connectin/genetics
Transfection
DNA Mutational Analysis
Adult
Female
Cardiomyopathy, Dilated/genetics
Cell Line
Genetic Predisposition to Disease
Genetic Association Studies
Models, Cardiovascular
Rats
Heredity
Haploinsufficiency
Phenotype
Animals
Muscle Contraction
Pedigree
Protein Isoforms
Heterozygote
Aged
Mutation
Źródło :
Beqqali, A, Bollen, I A E, Rasmussen, T B, van den Hoogenhof, M M, van Deutekom, H W M, Schafer-Korting, M, Haas, J, Meder, B, Sorensen, K E, van Oort, R J, Mogensen, J, Hubner, N, Creemers, E E, van der Velden, J & Pinto, Y M 2016, ' A mutation in the glutamate-rich region of RNA-binding motif protein 20 causes dilated cardiomyopathy through missplicing of titin and impaired Frank-Starling mechanism ', Cardiovascular Research, vol. 112, no. 1, pp. 452-463 . https://doi.org/10.1093/cvr/cvw192

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