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Wyszukujesz frazę ""Fibroblasts metabolism"" wg kryterium: Temat


Tytuł :
Charting DENR-dependent translation reinitiation uncovers predictive uORF features and links to circadian timekeeping via Clock
Autorzy :
Castelo-Szekely, Violeta
De Matos, Mara
Tusup, Marina
Pascolo, Steve
Ule, Jernej
Gatfield, David
Pokaż więcej
Temat :
5' Untranslated Regions
Animals
CLOCK Proteins/genetics
CLOCK Proteins/metabolism
Circadian Rhythm
Cloning, Molecular
Codon, Initiator
Eukaryotic Initiation Factors/genetics
Eukaryotic Initiation Factors/metabolism
Fibroblasts/metabolism
Gene Expression Regulation
HEK293 Cells
Humans
Luciferases/metabolism
Mice
Mutation
NIH 3T3 Cells
Open Reading Frames
RNA, Messenger/metabolism
Ribosomes/metabolism
Genetics
Dermatology Clinic
610 Medicine & health
Genomics
Źródło :
Nucleic acids research, vol. 47, no. 10, pp. 5193-5209
Castelo-Szekely, Violeta; De Matos, Mara; Tusup, Marina; Pascolo, Steve; Ule, Jernej; Gatfield, David (2019). Charting DENR-dependent translation reinitiation uncovers predictive uORF features and links to circadian timekeeping via Clock. Nucleic Acids Research, 47(10):5193-5209.
Opis pliku :
application/pdf
Tytuł :
Synchronized mechanical oscillations at the cell-matrix interface in the formation of tensile tissue
Autorzy :
Holmes, David F.
Yeung, Ching-Yan Chloé
Garva, Richa
Zindy, Egor
Taylor, Susan H.
Lu, Yinhui
Watson, Simon
Kalson, Nicholas S.
Kadler, Karl E.
Pokaż więcej
Temat :
Tensile Strength
Extracellular Matrix/metabolism
Cell Membrane/metabolism
PNAS Plus
Fibroblasts/metabolism
Humans
Stress, Mechanical
Źródło :
Holmes, D F, Yeung, C-Y C, Garva, R, Zindy, E, Taylor, S H, Lu, Y, Watson, S, Kalson, N S & Kadler, K E 2018, ' Synchronized mechanical oscillations at the cell-matrix interface in the formation of tensile tissue ', Proceedings of the National Academy of Sciences of the United States of America, vol. 115, no. 40, pp. E9288-E9297 . https://doi.org/10.1073/pnas.1801759115
Opis pliku :
application/pdf
Tytuł :
Biallelic RIPK1 mutations in humans cause severe immunodeficiency, arthritis and intestinal inflammation
Autorzy :
Cuchet-Lourenço, Delphine
Eletto, Davide
Plagnol, Vincent
Papapietro, Olivier
Bacon, Chris M
Alsaleem, Badr
Maes, Mailis
Alisaac, Ali
Goss, Emma
AlIdrissi, Eman
Wajant, Harald
Kumararatne, Dinakantha
Arkwright, Peter D
Abinun, Mario
Doffinger, Rainer
Nejentsev, Sergey
Wu, Changxin
Curtis, James
Ceron-Gutierrez, Lourdes
Hackett, Scott
Gaspar, Miguel
Siegmund, Daniela
AlZahrani, Mofareh S
Pokaż więcej
Temat :
Inflammatory Bowel Diseases
Receptor-Interacting Protein Serine-Threonine Kinases
Lymphopenia/genetics
Receptor-Interacting Protein Serine-Threonine Kinases/genetics
b_open_article_in_toll_access_journal
Fibroblasts/metabolism
Arthritis/genetics
Severe Combined Immunodeficiency
Article
Pedigree
Severe Combined Immunodeficiency/genetics
Mitogen-Activated Protein Kinases/metabolism
Fibroblasts
Arthritis
Inflammatory Bowel Diseases/genetics
Mitogen-Activated Protein Kinases
Cytokines
Alleles, Arthritis, Cytokines, Female, Fibroblasts, Humans, Inflammatory Bowel Diseases, Lymphopenia, Male, Mitogen-Activated Protein Kinases, Pedigree, Receptor-Interacting Protein Serine-Threonine Kinases, Severe Combined Immunodeficiency
Cytokines/metabolism
Female
Humans
Lymphopenia
Male
Alleles
Źródło :
Science, 361(6404), 810 - 813. American Association for the Advancement of Science
Science, 361 (6404) pp. 810-813. (2018)
Cuchet-Lourenço, D, Eletto, D, Wu, C, Plagnot, V, Papapietro, O, Curtis, J, Ceron-Gutierrez, L, Bacon, C M, Hackett, S, Alsaleem, B, Maes, M, Gaspar, M, Alisaac, A, Goos, E, Alidrissi, E, Siegmund, D, Wajant, H, Kumararatne, D, AlZahrani, M S, Arkwright, P, Abinun, M, Doffinger, R & Nejentsev, S 2018, ' Biallelic RIPK1 mutations in humans cause severe immunodeficiency, arthritis and intestinal inflammation ', Science . https://doi.org/10.1126/science.aar2641
Opis pliku :
Print-Electronic; text; application/pdf
Tytuł :
Mice knocked out for the primary brain calcification - associated gene Slc20a2 show unimpaired pre-natal survival but retarded growth and nodules in the brain that grow and calcify over time
Autorzy :
Jensen, Nina
Schrøder, Henrik D
Hejbøl, Eva K
Thomsen, Jesper S
Brüel, Annemarie
Larsen, Frederik T
Vinding, Mikkel C
Orlowski, Dariusz
Füchtbauer, Ernst-Martin
Oliveira, João Rm
Pedersen, Lene
Pokaż więcej
Temat :
Sodium-Phosphate Cotransporter Proteins, Type III/physiology
Cells, Cultured
Growth Disorders/physiopathology
Calcinosis/physiopathology
Fibroblasts/metabolism
Animals
Brain Diseases/physiopathology
Female
Mice
Mice, Knockout
Male
Animals, Newborn
Źródło :
Jensen, N, Schrøder, H D, Hejbøl, E K, Thomsen, J S, Brüel, A, Larsen, F T, Vinding, M C, Orlowski, D, Füchtbauer, E-M, Oliveira, J R & Pedersen, L 2018, ' Mice knocked out for the primary brain calcification associated gene Slc20a2 show unimpaired pre-natal survival but retarded growth and nodules in the brain that grow and calcify over time ', The American Journal of Pathology, vol. 188, no. 8, pp. 1865-1881 . https://doi.org/10.1016/j.ajpath.2018.04.010
Jensen, N, Schrøder, H D, Kildall Hejbøl, E, Thomsen, J S, Brüel, A, Larsen, F, Vinding, M C, Orlowski, D, Füchtbauer, E-M, Oliveira, J R M & Pedersen, L 2018, ' Mice knocked out for the primary brain calcification - associated gene Slc20a2 show unimpaired pre-natal survival but retarded growth and nodules in the brain that grow and calcify over time ', American Journal of Pathology, vol. 188, no. 8, pp. 1865-1881 . https://doi.org/10.1016/j.ajpath.2018.04.010
Opis pliku :
application/pdf
Tytuł :
Protein synthesis levels are increased in a subset of individuals with Fragile X syndrome
Autorzy :
Bagni, Claudia
Jacquemont, Sébastien
Pacini, Laura
Jønch, Aia E
Cencelli, Giulia
Rozenberg, Izabela
He, Yunsheng
D’Andrea, Laura
Pedini, Giorgia
Eldeeb, Marwa
Willemsen, Rob
Gasparini, Fabrizio
Tassone, Flora
Hagerman, Randi
Gomez-Mancilla, Baltazar
Pokaż więcej
Temat :
congenital, hereditary, and neonatal diseases and abnormalities
Autism Spectrum Disorder/genetics
Aged
Young Adult
Fibroblasts/metabolism
Fragile X Mental Retardation Protein/biosynthesis
Middle Aged
Mice
Mice, Knockout
Fragile X Syndrome/genetics
Neurons/metabolism
Disease Models, Animal
Corrigendum
Adolescent
Adult
Animals
Autism Spectrum Disorder/physiopathology
Child
Female
Fibroblasts/pathology
Fragile X Mental Retardation Protein/genetics
Fragile X Syndrome/physiopathology
Hippocampus/metabolism
Hippocampus/physiopathology
Humans
Male
Neurons/pathology
Articles
Źródło :
Human molecular genetics, vol. 27, no. 12, pp. 2039-2051
Human Molecular Genetics, 27(21)
Human Molecular Genetics, vol. 27, no. 21, pp. 3825
Human Molecular Genetics, 27(12), 2039 - 2051
Jacquemont, S, Pacini, L, Jønch, A E, Cencelli, G, Rozenberg, I, He, Y, D'Andrea, L, Pedini, G, Eldeeb, M, Willemsen, R, Gasparini, F, Tassone, F, Hagerman, R, Gomez-Mancilla, B & Bagni, C 2018, ' Protein synthesis levels are increased in a subset of individuals with Fragile X syndrome ', Human Molecular Genetics, vol. 27, no. 12, pp. 2039–2051 . https://doi.org/10.1093/hmg/ddy099
Opis pliku :
application/pdf
Tytuł :
TET2-mediated 5-hydroxymethylcytosine induces genetic instability and mutagenesis
Autorzy :
Mahfoudhi, Emna
Talhaoui, Ibtissam
Cabagnols, Xenia
Della Valle, Véronique
Secardin, Lise
Rameau, Philippe
Bernard, Olivier A
Ishchenko, Alexander A
Abbes, Salem
Vainchenker, William
Saparbaev, Murat
Plo, Isabelle
Pokaż więcej
Temat :
MESH: Animals
[SDV.MHEP] Life Sciences [q-bio]/Human health and pathology
MESH: 5-Methylcytosine/metabolism
MESH: DNA-Binding Proteins/metabolism
MESH: Cytosine/metabolism
[SDV.BC] Life Sciences [q-bio]/Cellular Biology
[SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Genomics [q-bio.GN]
TET2
MESH: Mutagenesis
MESH: Tumor Suppressor Protein p53/genetics
MESH: Genomic Instability
MESH: Megakaryocyte Progenitor Cells/cytology
MESH: Cell Line
MESH: 5-Methylcytosine/analogs & derivatives
MESH: Fibroblasts/cytology
MESH: B-Lymphocytes/cytology
MESH: DNA Repair
Genetic instability
MESH: Fibroblasts/metabolism
MESH: S Phase
MESH: Proto-Oncogene Proteins/metabolism
MESH: Megakaryocyte Progenitor Cells/metabolism
Cell cycle
5-hmC
MESH: Humans
MESH: Thymine DNA Glycosylase/genetics
MESH: Tumor Suppressor Protein p53/metabolism
MESH: Proto-Oncogene Proteins/genetics
MESH: Mice
MESH: Thymine DNA Glycosylase/deficiency
MESH: Epigenesis, Genetic
TDG
MESH: B-Lymphocytes/metabolism
MESH: Cytosine/analogs & derivatives
MESH: DNA-Binding Proteins/genetics
MESH: Base Sequence
MESH: Hydroxylation
Źródło :
DNA Repair, Elsevier, 2016, 43, pp.78 - 88. ⟨10.1016/j.dnarep.2016.05.031⟩
DNA Repair, Elsevier, 2016, 43, pp.78-88.

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