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Wyszukujesz frazę ""Gene Expression Regulation genetics"" wg kryterium: Temat


Tytuł :
The circadian clock components BMAL1 and REV-ERBα regulate flavivirus replication
Autorzy :
Lai, Alvina G
Donald, Claire L
Rudge, Simon Alan
Pinnick, Katherine
Wing, Peter AC
Qin, Ximing
Ray, David
Loudon, Andrew
Balfe, Peter
Wakelam, Michael
Butterworth, Sam
Zitzmann, Nicole
McKeating, Jane A
Zhuang, Xiaodong
Magri, Andrea
Hill, Michelle
Kumar, Abhinav
Rambhatla, Srinivasa Bhargav
Lopez-Clavijo, Andrea F
Chang, Wai Hoong
Brown, Ryan
Simmonds, Peter
Baumert, Thomas F
Kohl, Alain
Jopling, Catherine L
Pokaż więcej
Temat :
Essential/genetics
Hepacivirus/drug effects/genetics/metabolism
Messenger/metabolism
Dengue Virus/drug effects/genetics
Virus Replication
Circadian Clocks/*genetics/immunology
DNA Replication
Nuclear Receptor Subfamily 1, Group D, Member 1
Circadian Clocks
Virus Internalization
Zika Virus
Virus Replication/*drug effects
RNA, Messenger
Hepatocytes/immunology/virology
Cell Line
Flavivirus
ARNTL Transcription Factors
Zika Virus Infection
Virus Internalization/drug effects
viruses
Hepacivirus
Proteomics
RNA
Genes
Hepatitis C
Genes, Essential
Dengue Virus
Dengue
Hepatocytes
Article
Gene Expression Regulation
Nuclear Receptor Subfamily 1
Zika Virus/drug effects/genetics
Science
Gene Expression Regulation/genetics
ARNTL Transcription Factors/*genetics/immunology/pharmacology
Flavivirus/drug effects/*genetics/metabolism/pathogenicity
Humans
Member 1/*genetics/immunology/pharmacology
[SDV.MHEP]Life Sciences [q-bio]/Human health and pathology
Group D
Źródło :
Nature Communications, Nature Publishing Group, 2019, 10 (1), ⟨10.1038/s41467-019-08299-7⟩
Zhuang, X, Magri, A, Hill, M, Lai, A G, Kumar, A, Rambhatla, S B, Donald, C L, Lopez-Clavijo, A F, Rudge, S, Pinnick, K, Chang, W H, Wing, P A C, Brown, R, Qin, X, Simmonds, P, Baumert, T F, Ray, D, Loudon, A, Balfe, P, Wakelam, M, Butterworth, S, Kohl, A, Jopling, C L, Zitzmann, N & McKeating, J A 2019, ' The circadian clock components BMAL1 and REV-ERBα regulate flavivirus replication ', Nature Communications, vol. 10, no. 1, pp. 377 . https://doi.org/10.1038/s41467-019-08299-7
Nature Communications, Vol 10, Iss 1, Pp 1-13 (2019)
Opis pliku :
Electronic
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 :
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
Autorzy :
Demontis, Ditte
Walters, Raymond K.
Martin, Joanna
Mattheisen, Manuel
Als, Thomas D.
Agerbo, Esben
Baldursson, Gísli
Belliveau, Rich
Bybjerg-Grauholm, Jonas
Bækvad-Hansen, Marie
Cerrato, Felecia
Chambert, Kimberly
Churchhouse, Claire
Dumont, Ashley
Eriksson, Nicholas
Gandal, Michael
Goldstein, Jacqueline I.
Grasby, Katrina L.
Grove, Jakob
Gudmundsson, Olafur O.
Hansen, Christine S.
Hauberg, Mads Engel
Hollegaard, Mads V.
Howrigan, Daniel P.
Huang, Hailiang
Maller, Julian B.
Martin, Alicia R.
Martin, Nicholas G.
Moran, Jennifer
Pallesen, Jonatan
Palmer, Duncan S.
Pedersen, Carsten Bøcker
Pedersen, Marianne Giørtz
Poterba, Timothy
Poulsen, Jesper Buchhave
Ripke, Stephan
Robinson, Elise B.
Satterstrom, F. Kyle
Smith, George Davey
Davies, Gareth E.
Evans, David M.
Kemp, John P.
Ring, Susan
Stergiakouli, Evie
Pourcain, Beate St
Stoltenberg, Camilla
Timpson, Nicholas J.
Langley, Kate
Thapar, Anita
Medland, Sarah E.
Pokaż więcej
Temat :
Genetic Loci/genetics
Brain/physiology
Genome-Wide Association Study/methods
Research Support, Non-U.S. Gov't
Attention Deficit Disorder with Hyperactivity/genetics
behavioral disciplines and activities
Female
Child, Preschool
Meta-Analysis
mental disorders
Genetic Predisposition to Disease/genetics
Research Support, N.I.H., Extramural
Gene Expression Regulation/genetics
Cohort Studies
Adolescent
Risk
Journal Article
Humans
Male
Child
Polymorphism, Single Nucleotide/genetics
Źródło :
the 23 and Me Research Team, Demontis, D, Walters, R K, Martin, J, Mattheisen, M, Als, T D, Agerbo, E, Baldursson, G, Belliveau, R, Bybjerg-Grauholm, J, Bækvad-Hansen, M, Cerrato, F, Chambert, K, Churchhouse, C, Dumont, A, Eriksson, N, Gandal, M, Goldstein, J I, Grasby, K L, Grove, J, Gudmundsson, O O, Hansen, C S, Hauberg, M E, Hollegaard, M V, Howrigan, D P, Huang, H, Maller, J B, Martin, A R, Martin, N G, Moran, J, Pallesen, J, Palmer, D S, Pedersen, C B, Pedersen, M G, Poterba, T, Poulsen, J B, Ripke, S, Robinson, E B, Satterstrom, F K, Smith, G D, Davies, G E, Evans, D M, Kemp, J P, Ring, S, Stergiakouli, E, Pourcain, B S, Stoltenberg, C, Timpson, N J & Langley, K & Thapar, A & Medland, S E 2019, ' Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder ', Nature Genetics, vol. 51, no. 1, pp. 63-75 . https://doi.org/10.1038/s41588-018-0269-7
Opis pliku :
application/pdf
Tytuł :
RNA-mediated gene regulation is less evolvable than transcriptional regulation
Autorzy :
Payne, Joshua L
Khalid, Fahad
Wagner, Andreas
Pokaż więcej
Temat :
Multidisciplinary
empirical genotype-phenotype map
transcription factors
PNAS Plus
evolution
Biological Sciences
Animals
Binding Sites/genetics
DNA/metabolism
DNA-Binding Proteins/metabolism
Drosophila/genetics
Evolution, Molecular
Gene Expression Regulation/genetics
Gene Expression Regulation/physiology
Humans
Mutation
RNA/metabolism
RNA Processing, Post-Transcriptional/genetics
RNA-Binding Proteins/metabolism
Regulatory Sequences, Nucleic Acid
Transcription Factors/genetics
Transcription Factors/metabolism
Transcription, Genetic/genetics
RNA binding proteins
empirical genotype–phenotype map
gene regulation
Institute of Evolutionary Biology and Environmental Studies
590 Animals (Zoology)
570 Life sciences
biology
Źródło :
Proceedings of the National Academy of Sciences of the United States of America, vol. 115, no. 15, pp. E3481-E3490
Proceedings of the National Academy of Sciences of the United States of America, 115 (15)
Payne, Joshua L; Khalid, Fahad; Wagner, Andreas (2018). RNA-mediated gene regulation is less evolvable than transcriptional regulation. PNAS Proceedings of the National Academy of Sciences of the United States of America, 115(15):E3481-E3490.
Proceedings of the National Academy of Sciences of the United States of America
Opis pliku :
application/pdf; application/application/pdf
Tytuł :
A variant in a Cis-regulatory element enhances claudin-14 expression and is associated with pediatric-onset hypercalciuria and kidney stones
Autorzy :
Ure, Megan E
Heydari, Emma
Pan, Wanling
Ramesh, Ajay
Rehman, Sabah
Morgan, Catherine
Pinsk, Maury
Erickson, Robin
Herrmann, Johannes M
Dimke, Henrik
Cordat, Emmanuelle
Lemaire, Mathieu
Walter, Michael
Alexander, R Todd
Pokaż więcej
Temat :
Journal Article
hypercalciuria
claudin-14
pediatric kidney stones
Haplotypes
Protein Binding/genetics
Genetic Predisposition to Disease
Claudins/genetics
Humans
Child, Preschool
Infant
Male
Repressor Proteins/genetics
Binding Sites/genetics
Polymorphism, Single Nucleotide/genetics
Adolescent
Female
Hypercalciuria/complications
Calcium/blood
Child
Kidney Calculi/complications
Gene Expression Regulation/genetics
Źródło :
Ure, M E, Heydari, E, Pan, W, Ramesh, A, Rehman, S, Morgan, C, Pinsk, M, Erickson, R, Herrmann, J M, Dimke, H, Cordat, E, Lemaire, M, Walter, M & Alexander, R T 2017, ' A variant in a Cis-regulatory element enhances claudin-14 expression and is associated with pediatric-onset hypercalciuria and kidney stones ', Human Mutation, vol. 38, no. 6, pp. 649–657 . https://doi.org/10.1002/humu.23202

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