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Wyszukujesz frazę ""Nerve Tissue Proteins genetics"" wg kryterium: Temat


Tytuł :
An enhanced workflow for variant interpretation in UniProtKB/Swiss-Prot improves consistency and reuse in ClinVar
Autorzy :
Famiglietti, M L
Estreicher, A
Breuza, L
Poux, S
Redaschi, N
Xenarios, I
Bridge, A
Pokaż więcej
Temat :
Original Article
Copper-transporting ATPases/genetics
Databases, Protein
Genetic Variation
Knowledge Bases
Nerve Tissue Proteins/genetics
Workflow
Zinc Finger Protein Gli3/genetics
natural sciences
Źródło :
Database: The Journal of Biological Databases and Curation
Opis pliku :
application/pdf
Tytuł :
Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity.
Autorzy :
Kilpeläinen, T.O.
Bentley, A.R.
Noordam, R.
Sung, Y.J.
Schwander, K.
Winkler, T.W.
Jakupović, H.
Chasman, D.I.
Manning, A.
Ntalla, I.
Aschard, H.
Brown, M.R.
de Las Fuentes, L.
Franceschini, N.
Guo, X.
Vojinovic, D.
Aslibekyan, S.
Feitosa, M.F.
Kho, M.
Musani, S.K.
Richard, M.
Wang, H.
Wang, Z.
Bartz, T.M.
Bielak, L.F.
Campbell, A.
Dorajoo, R.
Fisher, V.
Hartwig, F.P.
Horimoto, ARVR
Li, C.
Lohman, K.K.
Marten, J.
Sim, X.
Smith, A.V.
Tajuddin, S.M.
Alver, M.
Amini, M.
Boissel, M.
Chai, J.F.
Chen, X.
Divers, J.
Evangelou, E.
Gao, C.
Graff, M.
Harris, S.E.
He, M.
Hsu, F.C.
Jackson, A.U.
Zhao, J.H.
Kraja, A.T.
Kühnel, B.
Laguzzi, F.
Lyytikäinen, L.P.
Nolte, I.M.
Rauramaa, R.
Riaz, M.
Robino, A.
Rueedi, R.
Stringham, H.M.
Takeuchi, F.
van der Most, P.J.
Varga, T.V.
Verweij, N.
Ware, E.B.
Wen, W.
Li, X.
Yanek, L.R.
Amin, N.
Arnett, D.K.
Boerwinkle, E.
Brumat, M.
Cade, B.
Canouil, M.
Chen, Y.I.
Concas, M.P.
Connell, J.
de Mutsert, R.
de Silva, H.J.
de Vries, P.S.
Demirkan, A.
Ding, J.
Eaton, C.B.
Faul, J.D.
Friedlander, Y.
Gabriel, K.P.
Ghanbari, M.
Giulianini, F.
Gu, C.C.
Gu, D.
Harris, T.B.
He, J.
Heikkinen, S.
Heng, C.K.
Hunt, S.C.
Ikram, M.A.
Jonas, J.B.
Koh, W.P.
Komulainen, P.
Krieger, J.E.
Kritchevsky, S.B.
Kutalik, Z.
Kuusisto, J.
Langefeld, C.D.
Langenberg, C.
Launer, L.J.
Leander, K.
Lemaitre, R.N.
Lewis, C.E.
Liang, J.
Liu, J.
Mägi, R.
Manichaikul, A.
Meitinger, T.
Metspalu, A.
Milaneschi, Y.
Mohlke, K.L.
Mosley, T.H.
Murray, A.D.
Nalls, M.A.
Nang, E.K.
Nelson, C.P.
Nona, S.
Norris, J.M.
Nwuba, C.V.
O'Connell, J.
Palmer, N.D.
Papanicolau, G.J.
Pazoki, R.
Pedersen, N.L.
Peters, A.
Peyser, P.A.
Polasek, O.
Porteous, D.J.
Poveda, A.
Raitakari, O.T.
Rich, S.S.
Risch, N.
Robinson, J.G.
Rose, L.M.
Rudan, I.
Schreiner, P.J.
Scott, R.A.
Sidney, S.S.
Sims, M.
Smith, J.A.
Snieder, H.
Sofer, T.
Starr, J.M.
Sternfeld, B.
Strauch, K.
Tang, H.
Taylor, K.D.
Tsai, M.Y.
Tuomilehto, J.
Uitterlinden, A.G.
van der Ende, M.Y.
van Heemst, D.
Voortman, T.
Waldenberger, M.
Wennberg, P.
Wilson, G.
Xiang, Y.B.
Yao, J.
Yu, C.
Yuan, J.M.
Zhao, W.
Zonderman, A.B.
Becker, D.M.
Boehnke, M.
Bowden, D.W.
de Faire, U.
Deary, I.J.
Elliott, P.
Esko, T.
Freedman, B.I.
Froguel, P.
Gasparini, P.
Gieger, C.
Kato, N.
Laakso, M.
Lakka, T.A.
Lehtimäki, T.
Magnusson, PKE
Oldehinkel, A.J.
Penninx, BWJH
Samani, N.J.
Shu, X.O.
van der Harst, P.
Van Vliet-Ostaptchouk, J.V.
Vollenweider, P.
Wagenknecht, L.E.
Wang, Y.X.
Wareham, N.J.
Weir, D.R.
Wu, T.
Zheng, W.
Zhu, X.
Evans, M.K.
Franks, P.W.
Gudnason, V.
Hayward, C.
Horta, B.L.
Kelly, T.N.
Liu, Y.
North, K.E.
Pereira, A.C.
Ridker, P.M.
Tai, E.S.
van Dam, R.M.
Fox, E.R.
Kardia, SLR
Liu, C.T.
Mook-Kanamori, D.O.
Province, M.A.
Redline, S.
van Duijn, C.M.
Rotter, J.I.
Kooperberg, C.B.
Gauderman, W.J.
Psaty, B.M.
Rice, K.
Munroe, P.B.
Fornage, M.
Cupples, L.A.
Rotimi, C.N.
Morrison, A.C.
Rao, D.C.
Loos, RJF
Pokaż więcej
Temat :
lipids (amino acids, peptides, and proteins)
Adolescent
Adult
African Continental Ancestry Group/genetics
Aged
Aged, 80 and over
Asian Continental Ancestry Group/genetics
Brazil
Calcium-Binding Proteins/genetics
Cholesterol/blood
Cholesterol, HDL/blood
Cholesterol, HDL/genetics
Cholesterol, LDL/blood
Cholesterol, LDL/genetics
European Continental Ancestry Group/genetics
Exercise
Female
Genetic Loci/genetics
Genome-Wide Association Study
Genotype
Hispanic Americans/genetics
Humans
LIM-Homeodomain Proteins/genetics
Lipid Metabolism/genetics
Lipids/blood
Lipids/genetics
Male
Membrane Proteins/genetics
Microtubule-Associated Proteins/genetics
Middle Aged
Muscle Proteins/genetics
Nerve Tissue Proteins/genetics
Transcription Factors/genetics
Triglycerides/blood
Triglycerides/genetics
Young Adult
Źródło :
Nature communications, vol. 10, no. 1, pp. 376
Opis pliku :
application/pdf
Tytuł :
Behavioral flexibility in a mouse model for obsessive-compulsive disorder: Impaired Pavlovian reversal learning in SAPAP3 mutants: Impaired Pavlovian reversal learning in SAPAP3 mutants
Autorzy :
van den Boom, Bastijn J. G.
Mooij, Adriana H.
Misevičiūtė, Ieva
Denys, Damiaan
Willuhn, Ingo
Pokaż więcej
Temat :
Animals
Conditioning, Classical
Female
Male
Mice
Mice, Inbred C57BL
Nerve Tissue Proteins/genetics
Obsessive-Compulsive Disorder/genetics
Źródło :
Genes, brain, and behavior, 18(4). Wiley-Blackwell
Tytuł :
Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants
Autorzy :
Pizzo, Lucilla
Jensen, Matthew
Polyak, Andrew
Rosenfeld, Jill A.
Mannik, Katrin
Krishnan, Arjun
McCready, Elizabeth
Pichon, Olivier
Le Caignec, Cedric
Van Dijck, Anke
Pope, Kate
Voorhoeve, Els
Yoon, Jieun
Stankiewicz, Paweł
Cheung, Sau Wai
Pazuchanics, Damian
Huber, Emily
Kumar, Vijay
Kember, Rachel L.
Mari, Francesca
Curró, Aurora
Castiglia, Lucia
Galesi, Ornella
Avola, Emanuela
Mattina, Teresa
Fichera, Marco
Mandarà, Luana
Vincent, Marie
Nizon, Mathilde
Mercier, Sandra
Bénéteau, Claire
Blesson, Sophie
Martin-Coignard, Dominique
Mosca-Boidron, Anne-Laure
Caberg, Jean-Hubert
Bucan, Maja
Zeesman, Susan
Nowaczyk, Małgorzata J. M.
Lefebvre, Mathilde
Faivre, Laurence
Callier, Patrick
Skinner, Cindy
Keren, Boris
Perrine, Charles
Prontera, Paolo
Marle, Nathalie
Renieri, Alessandra
Reymond, Alexandre
Kooy, R. Frank
Isidor, Bertrand
Schwartz, Charles
Romano, Corrado
Sistermans, Erik
Amor, David J.
Andrieux, Joris
Girirajan, Santhosh
Pokaż więcej
Temat :
Biology
phenotypic variability
16p11.2 deletion
autism
CNV
modifier
Genetics (clinical)
Autistic Disorder
Cell Adhesion Molecules, Neuronal
Chromosomes, Human, Pair 16
Cognition
DNA Copy Number Variations
Female
Gene Expression Regulation
Genetic Background
Humans
Male
Methyltransferases
Nerve Tissue Proteins
Parents
Pedigree
Phenotype
Proteins
Sequence Deletion
Siblings
Genetic Carrier Screening
Autistic Disorder/genetics
Autistic Disorder/physiopathology
Cell Adhesion Molecules, Neuronal/genetics
Chromosomes, Human, Pair 16/genetics
Cognition/physiology
DNA Copy Number Variations/genetics
Gene Expression Regulation/genetics
Methyltransferases/genetics
Nerve Tissue Proteins/genetics
Proteins/genetics
Sequence Deletion/genetics
[SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics
Human medicine
Article
Źródło :
Genetics in Medicine, Nature Publishing Group, In press, ⟨10.1038/s41436-018-0266-3⟩
Genetics in medicine : official journal of the American College of Medical Genetics
Genetics in medicine, vol. 21, no. 4, pp. 816-825
Opis pliku :
pdf; application/pdf
Tytuł :
Identification of expression quantitative trait loci associated with schizophrenia and affective disorders in normal brain tissue
Autorzy :
Bhalala, Oneil G
Inouye, Michael
Sibley, Christopher R
Nath, Artika P
UK Brain Expression Consortium
Pokaż więcej
Temat :
Nerve Tissue Proteins
Mood Disorders/diagnosis
Mood Disorders
Developmental Biology
Receptors, Nicotinic/genetics
Schizophrenia
Brain
Receptors, Nicotinic
Quantitative Trait Loci
Genotype
Gene Expression Regulation
UK Brain Expression Consortium
Nerve Tissue Proteins/genetics
Schizophrenia/diagnosis
QH426-470
Genetics
Polymorphism, Single Nucleotide
Genome-Wide Association Study
Brain/metabolism
Humans
0604 Genetics
Principal Component Analysis
Źródło :
2018, ' Identification of expression quantitative trait loci associated with schizophrenia and affective disorders in normal brain tissue ', PLoS Genetics, vol. 14, no. 8, pp. e1007607 . https://doi.org/10.1371/journal.pgen.1007607
PLoS Genetics, Vol 14, Iss 8, p e1007607 (2018)
Opis pliku :
Electronic-eCollection; application/pdf
Tytuł :
New insights into the pharmacogenomics of antidepressant response from the GENDEP and STAR*D studies:rare variant analysis and high-density imputation
Autorzy :
Fabbri, Chiara
Tansey, Katherine E.
Pokaż więcej
Temat :
Antidepressive Agents/adverse effects
Nerve Tissue Proteins/genetics
Pharmacogenetics/trends
Integrins/genetics
Genome-Wide Association Study
Polymorphism, Single Nucleotide
Genetics research, Predictive markers
Genetic Variation
Depressive Disorder, Major/drug therapy
Humans
Treatment Outcome
Genotype
Źródło :
Pharmacogenomics Journal, 18 pp. 413-422. (2017)
Fabbri, C, Tansey, K E, Perlis, R H, Hauser, J, Henigsberg, N, Maier, W, Mors, O, Placentino, A, Rietschel, M, Souery, D, Breen, G, Curtis, C, Sang-Hyuk, L, Newhouse, S, Patel, H, Guipponi, M, Perroud, N, Bondolfi, G, O'Donovan, M, Lewis, G, Biernacka, J M, Weinshilboum, R M, Farmer, A, Aitchison, K J, Craig, I, McGuffin, P, Uher, R & Lewis, C M 2018, ' New insights into the pharmacogenomics of antidepressant response from the GENDEP and STAR*D studies : rare variant analysis and high-density imputation ', The Pharmacogenomics Journal, vol. 18, no. 3, pp. 413-421 . https://doi.org/10.1038/tpj.2017.44
Opis pliku :
application/pdf; text
Tytuł :
TMEM59 potentiates Wnt signaling by promoting signalosome formation
Autorzy :
Tauriello, Daniele V. F.
Gerlach, Jan P.
Jordens, Ingrid
van ‘t Land-Kuper, Ineke
Bugter, Jeroen M.
Noordstra, Ivar
van der Kooij, Johanneke
Low, Teck Y.
Pimentel-Muiños, Felipe X.
Xanthakis, Despina
Fenderico, Nicola
Rabouille, Catherine
Heck, Albert J. R.
Egan, David A.
Maurice, Madelon M.
Pokaż więcej
Temat :
Protein–protein interactions
Signalosome
Low Density Lipoprotein Receptor-Related Protein-6/genetics
PNAS Plus
Multiprotein Complexes/genetics
Mice
Biological Sciences
protein-protein interactions
Wnt signaling
Multimerization
Nerve Tissue Proteins/genetics
Wnt Signaling Pathway/physiology
Cell Biology
Frizzled
Animals
HEK293 Cells
Wnt3A Protein/genetics
Humans
Membrane Proteins/genetics
Źródło :
Proceedings of the National Academy of Sciences of the United States of America, 115(17), E3996
Proceedings of the National Academy of Sciences of the United States of America, 115(17), E3996 - E4005. National Academy of Sciences
Proceedings of the National Academy of Sciences of the United States of America
Opis pliku :
image/pdf
Tytuł :
Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways
Autorzy :
Howard, David M.
Adams, Mark J.
Shirali, Masoud
Coleman, Jonathan R. I.
Shen, Xueyi
Lewis, Cathryn M.
Smith, Daniel J.
Haley, Chris S.
McIntosh, Andrew M.
Clarke, Toni-Kim
Marioni, Riccardo E.
Davies, Gail
Alloza, Clara
Barbu, Miruna C.
Wigmore, Eleanor M.
Gibson, Jude
Hagenaars, Saskia P.
Ward, Joey
Sullivan, Patrick F.
Breen, Gerome
Deary, Ian J.
Pokaż więcej
Temat :
Phenotype
United Kingdom
Depressive Disorder, Major/genetics
Biomarkers/metabolism
Synaptic Transmission/genetics
Genetic Loci
Article
Gene Expression Regulation
Nerve Tissue Proteins/genetics
Biological Specimen Banks
Mechanotransduction, Cellular/genetics
Genome-Wide Association Study
Science
Cohort Studies
Genetic Predisposition to Disease
Depression/genetics
Synapses/genetics
Humans
International Classification of Diseases
Linkage Disequilibrium
Źródło :
Howard, D M, Adams, M J, Shirali, M, Clarke, T-K, Marioni, R E, Davies, G, Coleman, J R I, Alloza, C, Shen, X, Barbu, M C, Wigmore, E M, Gibson, J, Hagenaars, S P, Lewis, C M, Ward, J, Smith, D J, Sullivan, P F, Haley, C S, Breen, G, Deary, I J & McIntosh, A M 2018, ' Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways ', Nature Communications, vol. 9, no. 1, 1470 . https://doi.org/10.1038/s41467-018-03819-3
Nature Communications, Vol 9, Iss 1, Pp 1-10 (2018)
Howard, D M, Adams, M J, Shirali, M, Clarke, T-K, Marioni, R, Davies, G, Coleman, J R I, Alloza, C, Shen, X, Barbu, M, Wigmore, E, Gibson, J, Hagenaars, S P, Lewis, C M, Ward, J, Smith, D J, Sullivan, P F, Haley, C, Breen, G, Deary, I & McIntosh, A 2018, ' Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways ', Nature Communications, vol. 9, no. 1, 1470, pp. 1-10 . https://doi.org/10.1038/s41467-018-03819-3, https://doi.org/10.1038/s41467-018-03819-3, https://doi.org/10.1038/s41467-018-03819-3
Opis pliku :
application/pdf
Tytuł :
Gene expression profiling of fast- and slow-growing non-functioning gonadotroph pituitary adenomas
Autorzy :
Falch, Camilla Maria
Sundaram, Arvind Y M
Øystese, Kristin Astrid
Normann, Kjersti Ringvoll
Lekva, Tove
Silamikelis, Ivars
Eieland, Alexander Kirkeby
Andersen, Marianne Skovsager
Bollerslev, Jens
Olarescu, Nicoleta Cristina
Pokaż więcej
Temat :
Adaptor Proteins, Signal Transducing/genetics
Adenoma/genetics
Adult
Aged
Cadherins/genetics
Cell Adhesion Molecules/genetics
Cell Movement/genetics
Cyclic AMP-Dependent Protein Kinase Catalytic Subunits/genetics
Epithelial-Mesenchymal Transition/genetics
Female
Follicle Stimulating Hormone/metabolism
Gene Expression Profiling
Gene Expression Regulation, Neoplastic
Gene Silencing
Humans
In Vitro Techniques
Intracellular Signaling Peptides and Proteins/genetics
Luteinizing Hormone/metabolism
Male
Membrane Glycoproteins/genetics
Microtubule-Associated Proteins/genetics
Middle Aged
Myosin Type I/genetics
Nerve Tissue Proteins/genetics
Pituitary Neoplasms/genetics
Proto-Oncogene Proteins/genetics
RNA, Messenger/metabolism
Receptors, Cell Surface/genetics
Reverse Transcriptase Polymerase Chain Reaction
Ribonucleases/genetics
Sialoglycoproteins/genetics
Time Factors
Źródło :
Falch, C M, Sundaram, A Y M, Øystese, K A, Normann, K R, Lekva, T, Silamikelis, I, Eieland, A K, Andersen, M S, Bollerslev, J & Olarescu, N C 2018, ' Gene expression profiling of fast- and slow-growing non-functioning gonadotroph pituitary adenomas ', European Journal of Endocrinology, vol. 178, no. 3, pp. 295-307 . https://doi.org/10.1530/EJE-17-0702
Tytuł :
Maternal eating disorders affect offspring cord-blood DNA methylation::a prospective study
Autorzy :
Micali, Nadia
Kazmi, Nabila
Gaunt, Tom R.
Relton, Caroline
Pokaż więcej
Temat :
Cord blood
Comparative Study
Epigenetic
Fetal Blood/chemistry
ALSPAC
Young Adult
Eating disorders
Research
Research Support, Non-U.S. Gov't
Galectin 2/genetics
Nerve Tissue Proteins/genetics
Oxidoreductases Acting on CH-CH Group Donors/genetics
QH426-470
Genetics
Female
Prenatal Exposure Delayed Effects/genetics
Maternal eating disorder
Feeding and Eating Disorders/genetics
Pregnancy
Medicine
ALSPAC, Cord blood, Eating disorders, Epigenetic, Methylation
Linear Models
DNA methylation
ddc:616.89
Methylation
Genome-Wide Association Study
Prospective Studies
Journal Article
Adult
Humans
Male
Longitudinal Studies
Źródło :
Clinical Epigenetics, 9, Article 120. (2017)
Clinical Epigenetics, Vol. 9 (2017) P. 120
Kazmi, N, Gaunt, T, Relton, C & Micali, N 2017, ' Maternal eating disorders affect offspring cord-blood DNA methylation: a prospective study ', Clinical Epigenetics . https://doi.org/10.1186/s13148-017-0418-3
Clinical Epigenetics, Vol 9, Iss 1, Pp 1-8 (2017)
Opis pliku :
text; 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

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