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  1. Article ; Online: Noel Warner Ph.D.

    Preffer, Frederic / Dunne, Jack / Recktenwald, Diether / Blidy, Andrew / Lanier, Lewis / Trotter, Joe / Daley, Michael J

    Cytometry. Part B, Clinical cytometry

    2023  Volume 104, Issue 1, Page(s) 7–9

    MeSH term(s) Humans ; Flow Cytometry
    Language English
    Publishing date 2023-01-09
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2099657-3
    ISSN 1552-4957 ; 1552-4949 ; 0196-4763
    ISSN (online) 1552-4957
    ISSN 1552-4949 ; 0196-4763
    DOI 10.1002/cyto.b.22112
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  2. Article ; Online: Dopamine D

    Lewis, Mechelle M / Van Scoy, Lauren J / De Jesus, Sol / Hakun, Jonathan G / Eslinger, Paul J / Fernandez-Mendoza, Julio / Kong, Lan / Yang, Yang / Snyder, Bethany L / Loktionova, Natalia / Duvvuri, Sridhar / Gray, David L / Huang, Xuemei / Mailman, Richard B

    Biomolecules

    2023  Volume 13, Issue 5

    Abstract: ... metrics inadequately gauge efficacy in LsPD patients. We explored if a D ...

    Abstract Current pharmacotherapy has limited efficacy and/or intolerable side effects in late-stage Parkinson's disease (LsPD) patients whose daily life depends primarily on caregivers and palliative care. Clinical metrics inadequately gauge efficacy in LsPD patients. We explored if a D
    MeSH term(s) Humans ; Parkinson Disease/drug therapy ; Levodopa/therapeutic use ; Levodopa/adverse effects ; Dopamine Agonists/therapeutic use ; Antiparkinson Agents/therapeutic use ; Dopamine
    Chemical Substances Levodopa (46627O600J) ; Dopamine Agonists ; Antiparkinson Agents ; Dopamine (VTD58H1Z2X)
    Language English
    Publishing date 2023-05-12
    Publishing country Switzerland
    Document type Randomized Controlled Trial ; Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2701262-1
    ISSN 2218-273X ; 2218-273X
    ISSN (online) 2218-273X
    ISSN 2218-273X
    DOI 10.3390/biom13050829
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  3. Article ; Online: Precise Measurement of the D_{s}^{+} Lifetime at Belle II.

    Adachi, I / Aggarwal, L / Aihara, H / Akopov, N / Aloisio, A / Anh Ky, N / Asner, D M / Atmacan, H / Aushev, T / Aushev, V / Aversano, M / Babu, V / Bae, H / Bahinipati, S / Bambade, P / Banerjee, Sw / Barrett, M / Baudot, J / Bauer, M /
    Baur, A / Beaubien, A / Becker, J / Behera, P K / Bennett, J V / Bernlochner, F U / Bertacchi, V / Bertemes, M / Bertholet, E / Bessner, M / Bettarini, S / Bhuyan, B / Bianchi, F / Bilka, T / Biswas, D / Bodrov, D / Bondar, A / Bozek, A / Bračko, M / Branchini, P / Briere, R A / Browder, T E / Budano, A / Bussino, S / Campajola, M / Cao, L / Casarosa, G / Cecchi, C / Cerasoli, J / Chang, M-C / Chang, P / Cheema, P / Chekelian, V / Cheon, B G / Chilikin, K / Chirapatpimol, K / Cho, H-E / Cho, K / Choi, S-K / Choudhury, S / Cochran, J / Corona, L / Das, S / Dattola, F / De La Motte, S A / de Marino, G / De Nardo, G / De Nuccio, M / De Pietro, G / de Sangro, R / Destefanis, M / Dey, S / Dhamija, R / Di Canto, A / Di Capua, F / Dingfelder, J / Doležal, Z / Domínguez Jiménez, I / Dong, T V / Dorigo, M / Dort, K / Dreyer, S / Dubey, S / Dujany, G / Ecker, P / Epifanov, D / Feichtinger, P / Ferlewicz, D / Finck, C / Finocchiaro, G / Fodor, A / Forti, F / Frey, A / Fulsom, B G / Gabrielli, A / Ganiev, E / Garcia-Hernandez, M / Garmash, A / Gaudino, G / Gaur, V / Gaz, A / Gellrich, A / Ghevondyan, G / Ghosh, D / Ghumaryan, H / Giakoustidis, G / Giordano, R / Giri, A / Glazov, A / Gobbo, B / Godang, R / Gogota, O / Goldenzweig, P / Gradl, W / Graziani, E / Greenwald, D / Gruberová, Z / Gu, T / Guan, Y / Gudkova, K / Han, Y / Hayasaka, K / Hayashii, H / Hazra, S / Hearty, C / Heredia de la Cruz, I / Hershenhorn, A / Higuchi, T / Hill, E C / Hoek, M / Hohmann, M / Hsu, C-L / Humair, T / Iijima, T / Inami, K / Ipsita, N / Ishikawa, A / Ito, S / Itoh, R / Iwasaki, M / Jackson, P / Jacobs, W W / Jaffe, D E / Jang, E-J / Ji, Q P / Jia, S / Jin, Y / Junkerkalefeld, H / Kaliyar, A B / Kandra, J / Karyan, G / Kawasaki, T / Keil, F / Ketter, C / Kiesling, C / Kim, C-H / Kim, D Y / Kim, K-H / Kim, Y-K / Kindo, H / Kinoshita, K / Kodyš, P / Koga, T / Kohani, S / Kojima, K / Korobov, A / Korpar, S / Kowalewski, R / Kraetzschmar, T M G / Križan, P / Krokovny, P / Kuhr, T / Kumar, J / Kumar, M / Kumar, R / Kumara, K / Kuzmin, A / Kwon, Y-J / Lacaprara, S / Lai, Y-T / Lam, T / Lange, J S / Laurenza, M / Leboucher, R / Le Diberder, F R / Leitl, P / Levit, D / Lewis, P M / Li, L K / Libby, J / Liu, Q Y / Liu, Z Q / Liventsev, D / Longo, S / Lueck, T / Lyu, C / Ma, Y / Maggiora, M / Maharana, S P / Maiti, R / Maity, S / Manfredi, R / Manoni, E / Mantovano, M / Marcantonio, D / Marcello, S / Marinas, C / Martellini, C / Martini, A / Martinov, T / Massaccesi, L / Masuda, M / Matsuda, T / Matsuoka, K / Matvienko, D / Maurya, S K / McKenna, J A / Mehta, R / Meier, F / Merola, M / Metzner, F / Milesi, M / Miller, C / Mirra, M / Miyabayashi, K / Mohanty, G B / Molina-Gonzalez, N / Mondal, S / Moneta, S / Moser, H-G / Mrvar, M / Mussa, R / Nakamura, I / Nakazawa, Y / Narimani Charan, A / Naruki, M / Natkaniec, Z / Natochii, A / Nayak, L / Nazaryan, G / Nisar, N K / Nishida, S / Ono, H / Otani, F / Oxford, E R / Pakhlov, P / Pakhlova, G / Paladino, A / Panta, A / Paoloni, E / Pardi, S / Passeri, A / Patra, S / Paul, S / Pedlar, T K / Peruzzi, I / Peschke, R / Pestotnik, R / Pham, F / Piccolo, M / Piilonen, L E / Podobnik, T / Pokharel, S / Praz, C / Prell, S / Prencipe, E / Prim, M T / Purwar, H / Rados, P / Raeuber, G / Raiz, S / Reif, M / Reiter, S / Remnev, M / Ripp-Baudot, I / Rizzo, G / Roney, J M / Rostomyan, A / Rout, N / Russo, G / Sandilya, S / Sangal, A / Santelj, L / Sato, Y / Savinov, V / Scavino, B / Schmitt, C / Schwanda, C / Schwartz, A J / Seino, Y / Selce, A / Senyo, K / Serrano, J / Sevior, M E / Sfienti, C / Shan, W / Shi, X D / Shillington, T / Shiu, J-G / Shtol, D / Sibidanov, A / Simon, F / Sobie, R J / Sobotzik, M / Soffer, A / Sokolov, A / Solovieva, E / Spataro, S / Spruck, B / Starič, M / Stavroulakis, P / Stottler, Z S / Stroili, R / Sumihama, M / Svidras, H / Takahashi, M / Takizawa, M / Tamponi, U / Tanida, K / Tenchini, F / Tittel, O / Tonelli, D / Torassa, E / Trabelsi, K / Tsaklidis, I / Unger, K / Unno, Y / Uno, K / Uno, S / Urquijo, P / Ushiroda, Y / Vahsen, S E / van Tonder, R / Varvell, K E / Veronesi, M / Vismaya, V S / Vitale, L / Volpe, R / Wach, B / Wallner, S / Wang, E / Wang, M-Z / Wang, X L / Wang, Z / Warburton, A / Watanabe, M / Wessel, C / Won, E / Xu, X P / Yabsley, B D / Yamada, S / Yan, W / Yang, S B / Yoshihara, K / Yuan, C Z / Yusa, Y / Zhang, Y / Zhilich, V / Zhou, J S / Zhou, Q D / Zhukova, V I / Žlebčík, R

    Physical review letters

    2023  Volume 131, Issue 17, Page(s) 171803

    Abstract: We measure the lifetime of the D_{s}^{+} meson using a data sample of 207  fb^{-1} collected ... determined by fitting the decay-time distribution of a sample of 116×10^{3} D_{s}^{+}→ϕπ^{+} decays ... Our result is τ_{D_{s}^{+}}=(499.5±1.7±0.9)  fs, where the first uncertainty is statistical and the second is ...

    Abstract We measure the lifetime of the D_{s}^{+} meson using a data sample of 207  fb^{-1} collected by the Belle II experiment running at the SuperKEKB asymmetric-energy e^{+}e^{-} collider. The lifetime is determined by fitting the decay-time distribution of a sample of 116×10^{3} D_{s}^{+}→ϕπ^{+} decays. Our result is τ_{D_{s}^{+}}=(499.5±1.7±0.9)  fs, where the first uncertainty is statistical and the second is systematic. This result is significantly more precise than previous measurements.
    Language English
    Publishing date 2023-11-13
    Publishing country United States
    Document type Journal Article
    ZDB-ID 208853-8
    ISSN 1079-7114 ; 0031-9007
    ISSN (online) 1079-7114
    ISSN 0031-9007
    DOI 10.1103/PhysRevLett.131.171803
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  4. Article ; Online: A Dopamine D

    Yang, Yang / Lewis, Mechelle M / Kong, Lan / Mailman, Richard B

    The Journal of pharmacology and experimental therapeutics

    2022  Volume 382, Issue 2, Page(s) 88–99

    Abstract: ... D ...

    Abstract Methylphenidate is used widely to treat symptoms of attention-deficit/hyperactivity disorder (ADHD), but like other stimulants has significant side effects. This study used a rodent model (spontaneously hypertensive rat) of spatial working memory (sWM) to compare the effects of methylphenidate with the novel dopamine D
    MeSH term(s) Animals ; Attention Deficit Disorder with Hyperactivity/drug therapy ; Central Nervous System Stimulants/pharmacology ; Dopamine ; Dopamine Agonists/pharmacology ; Memory, Short-Term ; Methylphenidate/pharmacology ; Prefrontal Cortex ; Rats ; Receptors, Dopamine D1/physiology ; Retrospective Studies
    Chemical Substances Central Nervous System Stimulants ; Dopamine Agonists ; Receptors, Dopamine D1 ; Methylphenidate (207ZZ9QZ49) ; Dopamine (VTD58H1Z2X)
    Language English
    Publishing date 2022-06-05
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, N.I.H., Extramural
    ZDB-ID 3106-9
    ISSN 1521-0103 ; 0022-3565
    ISSN (online) 1521-0103
    ISSN 0022-3565
    DOI 10.1124/jpet.122.001215
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  5. Article ; Online: Dopamine D

    Yang, Yang / Lewis, Mechelle M / Huang, Xuemei / Dokholyan, Nikolay V / Mailman, Richard B

    The international journal of biochemistry & cell biology

    2022  Volume 148, Page(s) 106235

    Abstract: ... ligands for the dopamine D ...

    Abstract The awareness of the potential importance of functional selectivity/biased signaling has led to the discovery of biased compounds as both research tools and novel drugs. A major pan-receptor focus has been to identify GPCR-selective ligands that have bias in G protein-dependent vs. β-arrestin related signaling. Although this field has exploded during the past two decades, it is only recently that highly β-arrestin biased ligands for the dopamine D
    MeSH term(s) Animals ; Arrestins/metabolism ; Biology ; Dopamine/metabolism ; Ligands ; Neurophysiology ; Signal Transduction ; beta-Arrestin 1/metabolism ; beta-Arrestins/metabolism
    Chemical Substances Arrestins ; Ligands ; beta-Arrestin 1 ; beta-Arrestins ; Dopamine (VTD58H1Z2X)
    Language English
    Publishing date 2022-06-07
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1228429-4
    ISSN 1878-5875 ; 1357-2725
    ISSN (online) 1878-5875
    ISSN 1357-2725
    DOI 10.1016/j.biocel.2022.106235
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  6. Article: Lipophilic analogues of D-cysteine prevent and reverse physical dependence to fentanyl in male rats.

    Bates, James N / Getsy, Paulina M / Coffee, Gregory A / Baby, Santhosh M / MacFarlane, Peter M / Hsieh, Yee-Hsee / Knauss, Zackery T / Bubier, Jason A / Mueller, Devin / Lewis, Stephen J

    Frontiers in pharmacology

    2024  Volume 14, Page(s) 1336440

    Abstract: We examined whether co-injections of the cell-permeant D-cysteine analogues, D-cysteine ethyl ester ... D-CYSee) and D-cysteine ethyl amide (D-CYSea), prevent acquisition of physical dependence induced ... that had received co-injections of D-CYSee (250 μmol/kg, IV) or D-CYSea (100 μmol/kg, IV), but not D ...

    Abstract We examined whether co-injections of the cell-permeant D-cysteine analogues, D-cysteine ethyl ester (D-CYSee) and D-cysteine ethyl amide (D-CYSea), prevent acquisition of physical dependence induced by twice-daily injections of fentanyl, and reverse acquired dependence to these injections in freely-moving male Sprague Dawley rats. Injection of the opioid receptor antagonist, naloxone HCl (NLX, 1.5 mg/kg, IV), elicited a series of withdrawal phenomena that included cardiorespiratory and behavioral responses, and falls in body weight and body temperature, in rats that received 5 or 10 injections of fentanyl (125 μg/kg, IV), and the same number of vehicle co-injections. Regarding the development of physical dependence, the NLX-precipitated withdrawal phenomena were markedly reduced in fentanyl-injected rats that had received co-injections of D-CYSee (250 μmol/kg, IV) or D-CYSea (100 μmol/kg, IV), but not D-cysteine (250 μmol/kg, IV). Regarding reversal of established dependence to fentanyl, the NLX-precipitated withdrawal phenomena in rats that had received 10 injections of fentanyl (125 μg/kg, IV) was markedly reduced in rats that received co-injections of D-CYSee (250 μmol/kg, IV) or D-CYSea (100 μmol/kg, IV), but not D-cysteine (250 μmol/kg, IV), starting with injection 6 of fentanyl. This study provides evidence that co-injections of D-CYSee and D-CYSea prevent the acquisition of physical dependence, and reverse acquired dependence to fentanyl in male rats. The lack of effect of D-cysteine suggests that the enhanced cell-penetrability of D-CYSee and D-CYSea into cells, particularly within the brain, is key to their ability to interact with intracellular signaling events involved in acquisition to physical dependence to fentanyl.
    Language English
    Publishing date 2024-04-05
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2587355-6
    ISSN 1663-9812
    ISSN 1663-9812
    DOI 10.3389/fphar.2023.1336440
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  7. Article ; Online: Reply to A Drewnowski et al, O Devinsky, D A Booth and E L Gibson, and D J Millward.

    Ludwig, David S / Aronne, Louis J / Astrup, Arne / de Cabo, Rafael / Cantley, Lewis C / Friedman, Mark I / Heymsfield, Steven B / Johnson, James D / King, Janet C / Krauss, Ronald M / Lieberman, Daniel E / Taubes, Gary / Volek, Jeff S / Westman, Eric C / Willett, Walter C / Yancy, William S / Ebbeling, Cara B

    The American journal of clinical nutrition

    2022  Volume 115, Issue 2, Page(s) 595–597

    Language English
    Publishing date 2022-02-09
    Publishing country United States
    Document type Letter ; Comment
    ZDB-ID 280048-2
    ISSN 1938-3207 ; 0002-9165
    ISSN (online) 1938-3207
    ISSN 0002-9165
    DOI 10.1093/ajcn/nqab385
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  8. Article ; Online: Arrestin-3 Agonism at Dopamine D

    Schamiloglu, Selin / Lewis, Elinor / Keeshen, Caroline M / Hergarden, Anne C / Bender, Kevin J / Whistler, Jennifer L

    Biological psychiatry

    2023  Volume 94, Issue 7, Page(s) 531–542

    Abstract: ... this unpredictability in treatment efficacy remain unclear. All SGAs bind the dopamine D: Methods: Here, we used ...

    Abstract Background: Second-generation antipsychotics (SGAs) are frontline treatments for serious mental illness. Often, individual patients benefit only from some SGAs and not others. The mechanisms underlying this unpredictability in treatment efficacy remain unclear. All SGAs bind the dopamine D
    Methods: Here, we used a combination of two-photon calcium imaging, in vitro signaling assays, and mouse behavior to assess signaling by SGAs at D3R.
    Results: We report that some clinically important SGAs function as arrestin-3 agonists at D3R, resulting in modulation of calcium channels localized to the site of action potential initiation in prefrontal cortex pyramidal neurons. We further show that chronic treatment with an arrestin-3 agonist SGA, but not an antagonist SGA, abolishes D3R function through postendocytic receptor degradation by GASP1 (G protein-coupled receptor-associated sorting protein-1).
    Conclusions: These results implicate D3R-arrestin-3 signaling as a source of SGA variability, highlighting the importance of including arrestin-3 signaling in characterizations of drug action. Furthermore, they suggest that postendocytic receptor trafficking that occurs during chronic SGA treatment may contribute to treatment efficacy.
    MeSH term(s) Mice ; Animals ; Dopamine ; beta-Arrestin 2/metabolism ; Antipsychotic Agents/pharmacology ; Receptors, Dopamine D3/metabolism ; Dopamine Agonists/pharmacology ; Drug Tolerance ; Receptors, Dopamine D1/metabolism
    Chemical Substances Dopamine (VTD58H1Z2X) ; beta-Arrestin 2 ; Antipsychotic Agents ; Receptors, Dopamine D3 ; Dopamine Agonists ; Receptors, Dopamine D1
    Language English
    Publishing date 2023-03-15
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 209434-4
    ISSN 1873-2402 ; 0006-3223
    ISSN (online) 1873-2402
    ISSN 0006-3223
    DOI 10.1016/j.biopsych.2023.03.006
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  9. Article ; Online: Chromatographic Phospholipid Trapping for Automated H/D Exchange Mass Spectrometry of Membrane Protein-Lipid Assemblies.

    Hammerschmid, Dietmar / Calvaresi, Valeria / Bailey, Chloe / Russell Lewis, Benjamin / Politis, Argyris / Morris, Michael / Denbigh, Laetitia / Anderson, Malcolm / Reading, Eamonn

    Analytical chemistry

    2023  Volume 95, Issue 5, Page(s) 3002–3011

    Abstract: ... with the ∼115 kDa transmembrane protein AcrB─proving efficient and automated phospholipid capture with minimal D ...

    Abstract Lipid interactions modulate the function, folding, structure, and organization of membrane proteins. Hydrogen/deuterium exchange mass spectrometry (HDX-MS) has emerged as a useful tool to understand the structural dynamics of these proteins within lipid environments. Lipids, however, have proven problematic for HDX-MS analysis of membrane-embedded proteins due to their presence of impairing proteolytic digestion, causing liquid chromatography column fouling, ion suppression, and/or mass spectral overlap. Herein, we describe the integration of a chromatographic phospholipid trap column into the HDX-MS apparatus to enable online sample delipidation prior to protease digestion of deuterium-labeled protein-lipid assemblies. We demonstrate the utility of this method on membrane scaffold protein-lipid nanodisc─both empty and loaded with the ∼115 kDa transmembrane protein AcrB─proving efficient and automated phospholipid capture with minimal D-to-H back-exchange, peptide carry-over, and protein loss. Our results provide insights into the efficiency of phospholipid capture by ZrO
    MeSH term(s) Phospholipids ; Deuterium ; Membrane Lipids ; Mass Spectrometry/methods ; Deuterium Exchange Measurement/methods ; Membrane Proteins ; Peptide Hydrolases
    Chemical Substances Phospholipids ; Deuterium (AR09D82C7G) ; Membrane Lipids ; Membrane Proteins ; Peptide Hydrolases (EC 3.4.-)
    Language English
    Publishing date 2023-01-27
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1508-8
    ISSN 1520-6882 ; 0003-2700
    ISSN (online) 1520-6882
    ISSN 0003-2700
    DOI 10.1021/acs.analchem.2c04876
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  10. Article ; Online: FGL1 as a modulator of plasma D-dimer levels: Exome-wide marker analysis of plasma tPA, PAI-1, and D-dimer.

    Thibord, Florian / Song, Ci / Pattee, Jack / Rodriguez, Benjamin A T / Chen, Ming-Huei / O'Donnell, Christopher J / Kleber, Marcus E / Delgado, Graciela E / Guo, Xiuqing / Yao, Jie / Taylor, Kent D / Ozel, Ayse Bilge / Brody, Jennifer A / McKnight, Barbara / Gyorgy, Beata / Simonsick, Eleanor / Leonard, Hampton L / Carrasquilla, Germán D / Guindo-Martinez, Marta /
    Silveira, Angela / Temprano-Sagrera, Gerard / Yanek, Lisa R / Becker, Diane M / Mathias, Rasika A / Becker, Lewis C / Raffield, Laura M / Kilpeläinen, Tuomas O / Grarup, Niels / Pedersen, Oluf / Hansen, Torben / Linneberg, Allan / Hamsten, Anders / Watkins, Hugh / Sabater-Lleal, Maria / Nalls, Mike A / Trégouët, David-Alexandre / Morange, Pierre-Emmanuel / Psaty, Bruce M / Tracy, Russel P / Smith, Nicholas L / Desch, Karl C / Cushman, Mary / Rotter, Jerome I / de Vries, Paul S / Pankratz, Nathan D / Folsom, Aaron R / Morrison, Alanna C / März, Winfried / Tang, Weihong / Johnson, Andrew D

    Journal of thrombosis and haemostasis : JTH

    2021  Volume 19, Issue 8, Page(s) 2019–2028

    Abstract: ... Plasminogen activator-inhibitor 1 (PAI-1), tissue plasminogen activator (tPA), and the plasma product D-dimer are ... studies of PAI-1, tPA, and D-dimer.: Objectives: We sought to discover new genetic loci contributing ... effects meta-analyses of PAI-1 (n = 15 603), tPA (n = 6876,) and D-dimer (n = 19 306) from 12 cohorts ...

    Abstract Background: Use of targeted exome-arrays with common, rare variants and functionally enriched variation has led to discovery of new genes contributing to population variation in risk factors. Plasminogen activator-inhibitor 1 (PAI-1), tissue plasminogen activator (tPA), and the plasma product D-dimer are important components of the fibrinolytic system. There have been few large-scale genome-wide or exome-wide studies of PAI-1, tPA, and D-dimer.
    Objectives: We sought to discover new genetic loci contributing to variation in these traits using an exome-array approach.
    Methods: Cohort-level analyses and fixed effects meta-analyses of PAI-1 (n = 15 603), tPA (n = 6876,) and D-dimer (n = 19 306) from 12 cohorts of European ancestry with diverse study design were conducted, including single-variant analyses and gene-based burden testing.
    Results: Five variants located in NME7, FGL1, and the fibrinogen locus, all associated with D-dimer levels, achieved genome-wide significance (P < 5 × 10
    Conclusion: This work provides new evidence for a role of FGL1 in hemostasis.
    MeSH term(s) Exome ; Fibrin Fibrinogen Degradation Products ; Fibrinogen/genetics ; Fibrinolysis ; Humans ; Plasminogen Activator Inhibitor 1/genetics ; Tissue Plasminogen Activator/genetics
    Chemical Substances FGL1 protein, human ; Fibrin Fibrinogen Degradation Products ; Plasminogen Activator Inhibitor 1 ; fibrin fragment D ; Fibrinogen (9001-32-5) ; Tissue Plasminogen Activator (EC 3.4.21.68)
    Language English
    Publishing date 2021-05-30
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, N.I.H., Intramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2112661-6
    ISSN 1538-7836 ; 1538-7933
    ISSN (online) 1538-7836
    ISSN 1538-7933
    DOI 10.1111/jth.15345
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