These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

359 related articles for article (PubMed ID: 32135084)

  • 1. Pathogenic DDX3X Mutations Impair RNA Metabolism and Neurogenesis during Fetal Cortical Development.
    Lennox AL; Hoye ML; Jiang R; Johnson-Kerner BL; Suit LA; Venkataramanan S; Sheehan CJ; Alsina FC; Fregeau B; Aldinger KA; Moey C; Lobach I; Afenjar A; Babovic-Vuksanovic D; Bézieau S; Blackburn PR; Bunt J; Burglen L; Campeau PM; Charles P; Chung BHY; Cogné B; Curry C; D'Agostino MD; Di Donato N; Faivre L; Héron D; Innes AM; Isidor B; Keren B; Kimball A; Klee EW; Kuentz P; Küry S; Martin-Coignard D; Mirzaa G; Mignot C; Miyake N; Matsumoto N; Fujita A; Nava C; Nizon M; Rodriguez D; Blok LS; Thauvin-Robinet C; Thevenon J; Vincent M; Ziegler A; Dobyns W; Richards LJ; Barkovich AJ; Floor SN; Silver DL; Sherr EH
    Neuron; 2020 May; 106(3):404-420.e8. PubMed ID: 32135084
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Aberrant cortical development is driven by impaired cell cycle and translational control in a
    Hoye ML; Calviello L; Poff AJ; Ejimogu NE; Newman CR; Montgomery MD; Ou J; Floor SN; Silver DL
    Elife; 2022 Jun; 11():. PubMed ID: 35762573
    [TBL] [Abstract][Full Text] [Related]  

  • 3. DDX3X syndrome: From clinical phenotypes to biological insights.
    von Mueffling A; Garcia-Forn M; De Rubeis S
    J Neurochem; 2024 Sep; 168(9):2147-2154. PubMed ID: 38976626
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel de novo DDX3X missense variant in a female with brachycephaly and intellectual disability: a case report.
    Moresco G; Costanza J; Santaniello C; Rondinone O; Grilli F; Prada E; Orcesi S; Coro I; Pichiecchio A; Marchisio P; Miozzo M; Fontana L; Milani D
    Ital J Pediatr; 2021 Mar; 47(1):81. PubMed ID: 33789733
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling.
    Snijders Blok L; Madsen E; Juusola J; Gilissen C; Baralle D; Reijnders MR; Venselaar H; Helsmoortel C; Cho MT; Hoischen A; Vissers LE; Koemans TS; Wissink-Lindhout W; Eichler EE; Romano C; Van Esch H; Stumpel C; Vreeburg M; Smeets E; Oberndorff K; van Bon BW; Shaw M; Gecz J; Haan E; Bienek M; Jensen C; Loeys BL; Van Dijck A; Innes AM; Racher H; Vermeer S; Di Donato N; Rump A; Tatton-Brown K; Parker MJ; Henderson A; Lynch SA; Fryer A; Ross A; Vasudevan P; Kini U; Newbury-Ecob R; Chandler K; Male A; ; Dijkstra S; Schieving J; Giltay J; van Gassen KL; Schuurs-Hoeijmakers J; Tan PL; Pediaditakis I; Haas SA; Retterer K; Reed P; Monaghan KG; Haverfield E; Natowicz M; Myers A; Kruer MC; Stein Q; Strauss KA; Brigatti KW; Keating K; Burton BK; Kim KH; Charrow J; Norman J; Foster-Barber A; Kline AD; Kimball A; Zackai E; Harr M; Fox J; McLaughlin J; Lindstrom K; Haude KM; van Roozendaal K; Brunner H; Chung WK; Kooy RF; Pfundt R; Kalscheuer V; Mehta SG; Katsanis N; Kleefstra T
    Am J Hum Genet; 2015 Aug; 97(2):343-52. PubMed ID: 26235985
    [TBL] [Abstract][Full Text] [Related]  

  • 6. De novo DDX3X missense variants in males appear viable and contribute to syndromic intellectual disability.
    Nicola P; Blackburn PR; Rasmussen KJ; Bertsch NL; Klee EW; Hasadsri L; Pichurin PN; Rankin J; Raymond FL; ; Clayton-Smith J
    Am J Med Genet A; 2019 Apr; 179(4):570-578. PubMed ID: 30734472
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic and phenotypic findings in 34 novel Spanish patients with DDX3X neurodevelopmental disorder.
    Parra A; Pascual P; Cazalla M; Arias P; Gallego-Zazo N; San-Martín EA; Silván C; Santos-Simarro F; ; Nevado J; Tenorio-Castano J; Lapunzina P
    Clin Genet; 2024 Feb; 105(2):140-149. PubMed ID: 37904618
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A comprehensive review on DDX3X liquid phase condensation in health and neurodevelopmental disorders.
    Rosa E Silva I; Smetana JHC; de Oliveira JF
    Int J Biol Macromol; 2024 Feb; 259(Pt 2):129330. PubMed ID: 38218270
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A hypomorphic inherited pathogenic variant in DDX3X causes male intellectual disability with additional neurodevelopmental and neurodegenerative features.
    Kellaris G; Khan K; Baig SM; Tsai IC; Zamora FM; Ruggieri P; Natowicz MR; Katsanis N
    Hum Genomics; 2018 Mar; 12(1):11. PubMed ID: 29490693
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Unwind and Relax: DDX3X RNA Helicase as a Critical Mediator of Cortical Neurogenesis.
    Vuocolo B; Holder JL
    Neuron; 2020 May; 106(3):357-358. PubMed ID: 32380046
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Three de novo DDX3X variants associated with distinctive brain developmental abnormalities and brain tumor in intellectually disabled females.
    Scala M; Torella A; Severino M; Morana G; Castello R; Accogli A; Verrico A; Vari MS; Cappuccio G; Pinelli M; Vitiello G; Terrone G; D'Amico A; ; Nigro V; Capra V
    Eur J Hum Genet; 2019 Aug; 27(8):1254-1259. PubMed ID: 30936465
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutations in genes encoding regulators of mRNA decapping and translation initiation: links to intellectual disability.
    Weil D; Piton A; Lessel D; Standart N
    Biochem Soc Trans; 2020 Jun; 48(3):1199-1211. PubMed ID: 32412080
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Developmental and Behavioral Phenotypes in a Mouse Model of DDX3X Syndrome.
    Boitnott A; Garcia-Forn M; Ung DC; Niblo K; Mendonca D; Park Y; Flores M; Maxwell S; Ellegood J; Qiu LR; Grice DE; Lerch JP; Rasin MR; Buxbaum JD; Drapeau E; De Rubeis S
    Biol Psychiatry; 2021 Dec; 90(11):742-755. PubMed ID: 34344536
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Paralog Studies Augment Gene Discovery: DDX and DHX Genes.
    Paine I; Posey JE; Grochowski CM; Jhangiani SN; Rosenheck S; Kleyner R; Marmorale T; Yoon M; Wang K; Robison R; Cappuccio G; Pinelli M; Magli A; Coban Akdemir Z; Hui J; Yeung WL; Wong BKY; Ortega L; Bekheirnia MR; Bierhals T; Hempel M; Johannsen J; Santer R; Aktas D; Alikasifoglu M; Bozdogan S; Aydin H; Karaca E; Bayram Y; Ityel H; Dorschner M; White JJ; Wilichowski E; Wortmann SB; Casella EB; Kitajima JP; Kok F; Monteiro F; Muzny DM; Bamshad M; Gibbs RA; Sutton VR; ; Van Esch H; Brunetti-Pierri N; Hildebrandt F; Brautbar A; Van den Veyver IB; Glass I; Lessel D; Lyon GJ; Lupski JR
    Am J Hum Genet; 2019 Aug; 105(2):302-316. PubMed ID: 31256877
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The variant landscape and function of DDX3X in cancer and neurodevelopmental disorders.
    Gadek M; Sherr EH; Floor SN
    Trends Mol Med; 2023 Sep; 29(9):726-739. PubMed ID: 37422363
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Medulloblastoma-associated mutations in the DEAD-box RNA helicase DDX3X/DED1 cause specific defects in translation.
    Brown NP; Vergara AM; Whelan AB; Guerra P; Bolger TA
    J Biol Chem; 2021; 296():100296. PubMed ID: 33460649
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Rare De Novo Missense Variants in RNA Helicase DDX6 Cause Intellectual Disability and Dysmorphic Features and Lead to P-Body Defects and RNA Dysregulation.
    Balak C; Benard M; Schaefer E; Iqbal S; Ramsey K; Ernoult-Lange M; Mattioli F; Llaci L; Geoffroy V; Courel M; Naymik M; Bachman KK; Pfundt R; Rump P; Ter Beest J; Wentzensen IM; Monaghan KG; McWalter K; Richholt R; Le Béchec A; Jepsen W; De Both M; Belnap N; Boland A; Piras IS; Deleuze JF; Szelinger S; Dollfus H; Chelly J; Muller J; Campbell A; Lal D; Rangasamy S; Mandel JL; Narayanan V; Huentelman M; Weil D; Piton A
    Am J Hum Genet; 2019 Sep; 105(3):509-525. PubMed ID: 31422817
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The Viral Protein K7 Inhibits Biochemical Activities and Condensate Formation by the DEAD-box Helicase DDX3X.
    Venus S; Tandjigora K; Jankowsky E
    J Mol Biol; 2023 Oct; 435(19):168217. PubMed ID: 37517790
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cancer-associated DDX3X mutations drive stress granule assembly and impair global translation.
    Valentin-Vega YA; Wang YD; Parker M; Patmore DM; Kanagaraj A; Moore J; Rusch M; Finkelstein D; Ellison DW; Gilbertson RJ; Zhang J; Kim HJ; Taylor JP
    Sci Rep; 2016 May; 6():25996. PubMed ID: 27180681
    [TBL] [Abstract][Full Text] [Related]  

  • 20. DDX3X Syndrome: Summary of Findings and Recommendations for Evaluation and Care.
    Levy T; Siper PM; Lerman B; Halpern D; Zweifach J; Belani P; Thurm A; Kleefstra T; Berry-Kravis E; Buxbaum JD; Grice DE
    Pediatr Neurol; 2023 Jan; 138():87-94. PubMed ID: 36434914
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.