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 *

211 related articles for article (PubMed ID: 35947077)

  • 1. Biallelic PAX5 mutations cause hypogammaglobulinemia, sensorimotor deficits, and autism spectrum disorder.
    Kaiser FMP; Gruenbacher S; Oyaga MR; Nio E; Jaritz M; Sun Q; van der Zwaag W; Kreidl E; Zopf LM; Dalm VASH; Pel J; Gaiser C; van der Vliet R; Wahl L; Rietman A; Hill L; Leca I; Driessen G; Laffeber C; Brooks A; Katsikis PD; Lebbink JHG; Tachibana K; van der Burg M; De Zeeuw CI; Badura A; Busslinger M
    J Exp Med; 2022 Sep; 219(9):. PubMed ID: 35947077
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Delineation of a novel neurodevelopmental syndrome associated with PAX5 haploinsufficiency.
    Gofin Y; Wang T; Gillentine MA; Scott TM; Berry AM; Azamian MS; Genetti C; Agrawal PB; Picker J; Wojcik MH; Delgado MR; Lynch SA; Scherer SW; Howe JL; Bacino CA; DiTroia S; VanNoy GE; O'Donnell-Luria A; Lalani SR; Graf WD; Rosenfeld JA; Eichler EE; Earl RK; Scott DA
    Hum Mutat; 2022 Apr; 43(4):461-470. PubMed ID: 35094443
    [TBL] [Abstract][Full Text] [Related]  

  • 3. GABAergic neurons regulate lateral ventricular development via transcription factor Pax5.
    Ohtsuka N; Badurek S; Busslinger M; Benes FM; Minichiello L; Rudolph U
    Genesis; 2013 Apr; 51(4):234-45. PubMed ID: 23349049
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Correction: Biallelic PAX5 mutations cause hypogammaglobulinemia, sensorimotor deficits, and autism spectrum disorder.
    Kaiser FMP; Gruenbacher S; Oyaga MR; Nio E; Jaritz M; Sun Q; van der Zwaag W; Kreidl E; Zopf LM; Dalm VASH; Pel J; Gaiser C; van der Vliet R; Wahl L; Rietman A; Hill L; Leca I; Driessen G; Laffeber C; Brooks A; Katsikis PD; Lebbink JHG; Tachibana K; van der Burg M; De Zeeuw CI; Badura A; Busslinger M
    J Exp Med; 2023 Jan; 220(1):. PubMed ID: 36480208
    [No Abstract]   [Full Text] [Related]  

  • 5. Monoallelic expression of Pax5: a paradigm for the haploinsufficiency of mammalian Pax genes?
    Nutt SL; Busslinger M
    Biol Chem; 1999 Jun; 380(6):601-11. PubMed ID: 10430025
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Characterization of three novel members of the zebrafish Pax2/5/8 family: dependency of Pax5 and Pax8 expression on the Pax2.1 (noi) function.
    Pfeffer PL; Gerster T; Lun K; Brand M; Busslinger M
    Development; 1998 Aug; 125(16):3063-74. PubMed ID: 9671580
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Ebf1 or Pax5 haploinsufficiency synergizes with STAT5 activation to initiate acute lymphoblastic leukemia.
    Heltemes-Harris LM; Willette MJ; Ramsey LB; Qiu YH; Neeley ES; Zhang N; Thomas DA; Koeuth T; Baechler EC; Kornblau SM; Farrar MA
    J Exp Med; 2011 Jun; 208(6):1135-49. PubMed ID: 21606506
    [TBL] [Abstract][Full Text] [Related]  

  • 8. PAX5 is part of a functional transcription factor network targeted in lymphoid leukemia.
    Okuyama K; Strid T; Kuruvilla J; Somasundaram R; Cristobal S; Smith E; Prasad M; Fioretos T; Lilljebjörn H; Soneji S; Lang S; Ungerbäck J; Sigvardsson M
    PLoS Genet; 2019 Aug; 15(8):e1008280. PubMed ID: 31381561
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Independent regulation of the two Pax5 alleles during B-cell development.
    Nutt SL; Vambrie S; Steinlein P; Kozmik Z; Rolink A; Weith A; Busslinger M
    Nat Genet; 1999 Apr; 21(4):390-5. PubMed ID: 10192389
    [TBL] [Abstract][Full Text] [Related]  

  • 10. NEXMIF/KIDLIA Knock-out Mouse Demonstrates Autism-Like Behaviors, Memory Deficits, and Impairments in Synapse Formation and Function.
    Gilbert J; O'Connor M; Templet S; Moghaddam M; Di Via Ioschpe A; Sinclair A; Zhu LQ; Xu W; Man HY
    J Neurosci; 2020 Jan; 40(1):237-254. PubMed ID: 31704787
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Early B-cell factor 1 regulates the expansion of B-cell progenitors in a dose-dependent manner.
    Åhsberg J; Ungerbäck J; Strid T; Welinder E; Stjernberg J; Larsson M; Qian H; Sigvardsson M
    J Biol Chem; 2013 Nov; 288(46):33449-61. PubMed ID: 24078629
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia.
    Shah S; Schrader KA; Waanders E; Timms AE; Vijai J; Miething C; Wechsler J; Yang J; Hayes J; Klein RJ; Zhang J; Wei L; Wu G; Rusch M; Nagahawatte P; Ma J; Chen SC; Song G; Cheng J; Meyers P; Bhojwani D; Jhanwar S; Maslak P; Fleisher M; Littman J; Offit L; Rau-Murthy R; Fleischut MH; Corines M; Murali R; Gao X; Manschreck C; Kitzing T; Murty VV; Raimondi S; Kuiper RP; Simons A; Schiffman JD; Onel K; Plon SE; Wheeler D; Ritter D; Ziegler DS; Tucker K; Sutton R; Chenevix-Trench G; Li J; Huntsman DG; Hansford S; Senz J; Walsh T; Lee M; Hahn CN; Roberts K; King MC; Lo SM; Levine RL; Viale A; Socci ND; Nathanson KL; Scott HS; Daly M; Lipkin SM; Lowe SW; Downing JR; Altshuler D; Sandlund JT; Horwitz MS; Mullighan CG; Offit K
    Nat Genet; 2013 Oct; 45(10):1226-1231. PubMed ID: 24013638
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Postnatal Tshz3 Deletion Drives Altered Corticostriatal Function and Autism Spectrum Disorder-like Behavior.
    Chabbert D; Caubit X; Roubertoux PL; Carlier M; Habermann B; Jacq B; Salin P; Metwaly M; Frahm C; Fatmi A; Garratt AN; Severac D; Dubois E; Kerkerian-Le Goff L; Fasano L; Gubellini P
    Biol Psychiatry; 2019 Aug; 86(4):274-285. PubMed ID: 31060802
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Early communication deficits in the Shank1 knockout mouse model for autism spectrum disorder: Developmental aspects and effects of social context.
    Sungur AÖ; Schwarting RK; Wöhr M
    Autism Res; 2016 Jun; 9(6):696-709. PubMed ID: 26419918
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Inhibition of inflammatory signaling in Pax5 mutant cells mitigates B-cell leukemogenesis.
    Isidro-Hernández M; Mayado A; Casado-García A; Martínez-Cano J; Palmi C; Fazio G; Orfao A; Ribera J; Ribera JM; Zamora L; Raboso-Gallego J; Blanco O; Alonso-López D; De Las Rivas J; Jiménez R; García Criado FJ; García Cenador MB; Ramírez-Orellana M; Cazzaniga G; Cobaleda C; Vicente-Dueñas C; Sánchez-García I
    Sci Rep; 2020 Nov; 10(1):19189. PubMed ID: 33154497
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Combined heterozygous loss of Ebf1 and Pax5 allows for T-lineage conversion of B cell progenitors.
    Ungerbäck J; Åhsberg J; Strid T; Somasundaram R; Sigvardsson M
    J Exp Med; 2015 Jun; 212(7):1109-23. PubMed ID: 26056231
    [TBL] [Abstract][Full Text] [Related]  

  • 17. PAX5 biallelic genomic alterations define a novel subgroup of B-cell precursor acute lymphoblastic leukemia.
    Bastian L; Schroeder MP; Eckert C; Schlee C; Tanchez JO; Kämpf S; Wagner DL; Schulze V; Isaakidis K; Lázaro-Navarro J; Hänzelmann S; James AR; Ekici A; Burmeister T; Schwartz S; Schrappe M; Horstmann M; Vosberg S; Krebs S; Blum H; Hecht J; Greif PA; Rieger MA; Brüggemann M; Gökbuget N; Neumann M; Baldus CD
    Leukemia; 2019 Aug; 33(8):1895-1909. PubMed ID: 30842609
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Pax5 loss imposes a reversible differentiation block in B-progenitor acute lymphoblastic leukemia.
    Liu GJ; Cimmino L; Jude JG; Hu Y; Witkowski MT; McKenzie MD; Kartal-Kaess M; Best SA; Tuohey L; Liao Y; Shi W; Mullighan CG; Farrar MA; Nutt SL; Smyth GK; Zuber J; Dickins RA
    Genes Dev; 2014 Jun; 28(12):1337-50. PubMed ID: 24939936
    [TBL] [Abstract][Full Text] [Related]  

  • 19. One missense mutation in exon 2 of the PAX5 gene in Iran.
    Yazdanparast S; Khatami SR; Galehdari H; Jaseb K
    Genet Mol Res; 2015 Dec; 14(4):17768-75. PubMed ID: 26782422
    [TBL] [Abstract][Full Text] [Related]  

  • 20. PAX5-driven subtypes of B-progenitor acute lymphoblastic leukemia.
    Gu Z; Churchman ML; Roberts KG; Moore I; Zhou X; Nakitandwe J; Hagiwara K; Pelletier S; Gingras S; Berns H; Payne-Turner D; Hill A; Iacobucci I; Shi L; Pounds S; Cheng C; Pei D; Qu C; Newman S; Devidas M; Dai Y; Reshmi SC; Gastier-Foster J; Raetz EA; Borowitz MJ; Wood BL; Carroll WL; Zweidler-McKay PA; Rabin KR; Mattano LA; Maloney KW; Rambaldi A; Spinelli O; Radich JP; Minden MD; Rowe JM; Luger S; Litzow MR; Tallman MS; Racevskis J; Zhang Y; Bhatia R; Kohlschmidt J; Mrózek K; Bloomfield CD; Stock W; Kornblau S; Kantarjian HM; Konopleva M; Evans WE; Jeha S; Pui CH; Yang J; Paietta E; Downing JR; Relling MV; Zhang J; Loh ML; Hunger SP; Mullighan CG
    Nat Genet; 2019 Feb; 51(2):296-307. PubMed ID: 30643249
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.