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 *

287 related articles for article (PubMed ID: 37978175)

  • 1. Mutation of key signaling regulators of cerebrovascular development in vein of Galen malformations.
    Zhao S; Mekbib KY; van der Ent MA; Allington G; Prendergast A; Chau JE; Smith H; Shohfi J; Ocken J; Duran D; Furey CG; Hao LT; Duy PQ; Reeves BC; Zhang J; Nelson-Williams C; Chen D; Li B; Nottoli T; Bai S; Rolle M; Zeng X; Dong W; Fu PY; Wang YC; Mane S; Piwowarczyk P; Fehnel KP; See AP; Iskandar BJ; Aagaard-Kienitz B; Moyer QJ; Dennis E; Kiziltug E; Kundishora AJ; DeSpenza T; Greenberg ABW; Kidanemariam SM; Hale AT; Johnston JM; Jackson EM; Storm PB; Lang SS; Butler WE; Carter BS; Chapman P; Stapleton CJ; Patel AB; Rodesch G; Smajda S; Berenstein A; Barak T; Erson-Omay EZ; Zhao H; Moreno-De-Luca A; Proctor MR; Smith ER; Orbach DB; Alper SL; Nicoli S; Boggon TJ; Lifton RP; Gunel M; King PD; Jin SC; Kahle KT
    Nat Commun; 2023 Nov; 14(1):7452. PubMed ID: 37978175
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic dysregulation of an endothelial Ras signaling network in vein of Galen malformations.
    Zhao S; Mekbib KY; van der Ent MA; Allington G; Prendergast A; Chau JE; Smith H; Shohfi J; Ocken J; Duran D; Furey CG; Le HT; Duy PQ; Reeves BC; Zhang J; Nelson-Williams C; Chen D; Li B; Nottoli T; Bai S; Rolle M; Zeng X; Dong W; Fu PY; Wang YC; Mane S; Piwowarczyk P; Fehnel KP; See AP; Iskandar BJ; Aagaard-Kienitz B; Kundishora AJ; DeSpenza T; Greenberg ABW; Kidanemariam SM; Hale AT; Johnston JM; Jackson EM; Storm PB; Lang SS; Butler WE; Carter BS; Chapman P; Stapleton CJ; Patel AB; Rodesch G; Smajda S; Berenstein A; Barak T; Erson-Omay EZ; Zhao H; Moreno-De-Luca A; Proctor MR; Smith ER; Orbach DB; Alper SL; Nicoli S; Boggon TJ; Lifton RP; Gunel M; King PD; Jin SC; Kahle KT
    bioRxiv; 2023 Mar; ():. PubMed ID: 36993588
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Human genetics and molecular mechanisms of vein of Galen malformation.
    Duran D; Karschnia P; Gaillard JR; Karimy JK; Youngblood MW; DiLuna ML; Matouk CC; Aagaard-Kienitz B; Smith ER; Orbach DB; Rodesch G; Berenstein A; Gunel M; Kahle KT
    J Neurosurg Pediatr; 2018 Apr; 21(4):367-374. PubMed ID: 29350590
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutations in Chromatin Modifier and Ephrin Signaling Genes in Vein of Galen Malformation.
    Duran D; Zeng X; Jin SC; Choi J; Nelson-Williams C; Yatsula B; Gaillard J; Furey CG; Lu Q; Timberlake AT; Dong W; Sorscher MA; Loring E; Klein J; Allocco A; Hunt A; Conine S; Karimy JK; Youngblood MW; Zhang J; DiLuna ML; Matouk CC; Mane S; Tikhonova IR; Castaldi C; López-Giráldez F; Knight J; Haider S; Soban M; Alper SL; Komiyama M; Ducruet AF; Zabramski JM; Dardik A; Walcott BP; Stapleton CJ; Aagaard-Kienitz B; Rodesch G; Jackson E; Smith ER; Orbach DB; Berenstein A; Bilguvar K; Vikkula M; Gunel M; Lifton RP; Kahle KT
    Neuron; 2019 Feb; 101(3):429-443.e4. PubMed ID: 30578106
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An ACVRL1 gene mutation presenting as vein of Galen malformation at prenatal diagnosis.
    De Luca C; Bevilacqua E; Badr DA; Cannie MM; Sanchez TC; Segers V; Keymolen K; Jani JC
    Am J Med Genet A; 2020 May; 182(5):1255-1258. PubMed ID: 32170914
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Angiogenesis depends upon EPHB4-mediated export of collagen IV from vascular endothelial cells.
    Chen D; Hughes ED; Saunders TL; Wu J; Vasquez MNH; Makinen T; King PD
    JCI Insight; 2022 Feb; 7(4):. PubMed ID: 35015735
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Germline Loss-of-Function Mutations in EPHB4 Cause a Second Form of Capillary Malformation-Arteriovenous Malformation (CM-AVM2) Deregulating RAS-MAPK Signaling.
    Amyere M; Revencu N; Helaers R; Pairet E; Baselga E; Cordisco M; Chung W; Dubois J; Lacour JP; Martorell L; Mazereeuw-Hautier J; Pyeritz RE; Amor DJ; Bisdorff A; Blei F; Bombei H; Dompmartin A; Brooks D; Dupont J; González-Enseñat MA; Frieden I; Gérard M; Kvarnung M; Hanson-Kahn AK; Hudgins L; Léauté-Labrèze C; McCuaig C; Metry D; Parent P; Paul C; Petit F; Phan A; Quere I; Salhi A; Turner A; Vabres P; Vicente A; Wargon O; Watanabe S; Weibel L; Wilson A; Willing M; Mulliken JB; Boon LM; Vikkula M
    Circulation; 2017 Sep; 136(11):1037-1048. PubMed ID: 28687708
    [TBL] [Abstract][Full Text] [Related]  

  • 8. EphrinB2-EphB4-RASA1 Signaling in Human Cerebrovascular Development and Disease.
    Zeng X; Hunt A; Jin SC; Duran D; Gaillard J; Kahle KT
    Trends Mol Med; 2019 Apr; 25(4):265-286. PubMed ID: 30819650
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Loss of function mutations in EPHB4 are responsible for vein of Galen aneurysmal malformation.
    Vivanti A; Ozanne A; Grondin C; Saliou G; Quevarec L; Maurey H; Aubourg P; Benachi A; Gut M; Gut I; Martinovic J; Sénat MV; Tawk M; Melki J
    Brain; 2018 Apr; 141(4):979-988. PubMed ID: 29444212
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Generation of mice with a conditional allele of the p120 Ras GTPase-activating protein.
    Lapinski PE; Bauler TJ; Brown EJ; Hughes ED; Saunders TL; King PD
    Genesis; 2007 Dec; 45(12):762-7. PubMed ID: 18064675
    [TBL] [Abstract][Full Text] [Related]  

  • 11. EPHB4 Mutation Implicated in Capillary Malformation-Arteriovenous Malformation Syndrome: A Case Report.
    Yu J; Streicher JL; Medne L; Krantz ID; Yan AC
    Pediatr Dermatol; 2017 Sep; 34(5):e227-e230. PubMed ID: 28730721
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cerebrovascular Anomalies in the Fetus.
    Jaimes C; Ferraciolli SF; Orbach DB
    AJNR Am J Neuroradiol; 2024 Sep; ():. PubMed ID: 38866434
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Deep venous communication in vein of Galen malformations: incidence, Imaging, and Implications for treatment.
    Kortman H; Navaei E; Raybaud CA; Bhatia KD; Shroff M; terBrugge K; Armstrong D; Pereira VM; Dirks PB; Krings T; Muthusami P
    J Neurointerv Surg; 2021 Mar; 13(3):290-293. PubMed ID: 32546638
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A case of capillary malformation-arteriovenous malformation and Ebstein's anomaly in a child with EphB4 mutation.
    Sherwani Y; Jenkins S; Adelanwa A; Burch DM; Chaudhuri NR; Zinn Z
    Pediatr Dermatol; 2021 Sep; 38(5):1305-1307. PubMed ID: 34339071
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Radiological and clinical features of vein of Galen malformations.
    Chow ML; Cooke DL; Fullerton HJ; Amans MR; Narvid J; Dowd CF; Higashida RT; Halbach VV; Hetts SW
    J Neurointerv Surg; 2015 Jun; 7(6):443-8. PubMed ID: 24789593
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Dural arteriovenous shunt development in patients with vein of galen malformation.
    Paramasivam S; Niimi Y; Meila D; Berenstein A
    Interv Neuroradiol; 2014 Dec; 20(6):781-90. PubMed ID: 25496691
    [TBL] [Abstract][Full Text] [Related]  

  • 17. RASA1 functions in EPHB4 signaling pathway to suppress endothelial mTORC1 activity.
    Kawasaki J; Aegerter S; Fevurly RD; Mammoto A; Mammoto T; Sahin M; Mably JD; Fishman SJ; Chan J
    J Clin Invest; 2014 Jun; 124(6):2774-84. PubMed ID: 24837431
    [TBL] [Abstract][Full Text] [Related]  

  • 18. EPHB4-RASA1-Mediated Negative Regulation of Ras-MAPK Signaling in the Vasculature: Implications for the Treatment of EPHB4- and RASA1-Related Vascular Anomalies in Humans.
    Chen D; Van der Ent MA; Lartey NL; King PD
    Pharmaceuticals (Basel); 2023 Jan; 16(2):. PubMed ID: 37259315
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Discovery and Characterization of Ephrin B2 and EphB4 Dysregulation and Novel Mutations in Cerebral Cavernous Malformations: In Vitro and Patient-Derived Evidence of Ephrin-Mediated Endothelial Cell Pathophysiology.
    Sesen J; Ghalali A; Driscoll J; Martinez T; Lupieri A; Zurakowski D; Alexandrescu S; Smith ER; Fehnel KP
    Cell Mol Neurobiol; 2023 Dec; 44(1):12. PubMed ID: 38150042
    [TBL] [Abstract][Full Text] [Related]  

  • 20. RASA1 somatic mutation and variable expressivity in capillary malformation/arteriovenous malformation (CM/AVM) syndrome.
    Macmurdo CF; Wooderchak-Donahue W; Bayrak-Toydemir P; Le J; Wallenstein MB; Milla C; Teng JM; Bernstein JA; Stevenson DA
    Am J Med Genet A; 2016 Jun; 170(6):1450-4. PubMed ID: 26969842
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.