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 *

147 related articles for article (PubMed ID: 35943828)

  • 21. Exome sequencing as first-tier test for fetuses with severe central nervous system structural anomalies.
    Yaron Y; Ofen Glassner V; Mory A; Zunz Henig N; Kurolap A; Bar Shira A; Brabbing Goldstein D; Marom D; Ben Sira L; Baris Feldman H; Malinger G; Krajden Haratz K; Reches A
    Ultrasound Obstet Gynecol; 2022 Jul; 60(1):59-67. PubMed ID: 35229910
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Fetal central nervous system anomalies: When should we offer exome sequencing?
    Baptiste C; Mellis R; Aggarwal V; Lord J; Eberhardt R; Kilby MD; Maher ER; Wapner R; Giordano J; Chitty L
    Prenat Diagn; 2022 May; 42(6):736-743. PubMed ID: 35411553
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Fetal intracerebral hemorrhage and cataract: think COL4A1.
    Colin E; Sentilhes L; Sarfati A; Mine M; Guichet A; Ploton C; Boussion F; Delorme B; Tournier-Lasserve E; Bonneau D
    J Perinatol; 2014 Jan; 34(1):75-7. PubMed ID: 24374867
    [TBL] [Abstract][Full Text] [Related]  

  • 24. COL4A2 mutation causing adult onset recurrent intracerebral hemorrhage and leukoencephalopathy.
    Gunda B; Mine M; Kovács T; Hornyák C; Bereczki D; Várallyay G; Rudas G; Audrezet MP; Tournier-Lasserve E
    J Neurol; 2014 Mar; 261(3):500-3. PubMed ID: 24390199
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Is there relation between COL4A1/A2 mutations and antenatally detected fetal intraventricular hemorrhage?
    Kutuk MS; Balta B; Kodera H; Matsumoto N; Saitsu H; Doganay S; Canpolat M; Dolanbay M; Unal E; Dundar M
    Childs Nerv Syst; 2014 Mar; 30(3):419-24. PubMed ID: 24317722
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Intracerebral hemorrhage and COL4A1 and COL4A2 mutations, from fetal life into adulthood.
    de Vries LS; Mancini GM
    Ann Neurol; 2012 Apr; 71(4):439-41. PubMed ID: 22447691
    [No Abstract]   [Full Text] [Related]  

  • 27. COL4A1 and COL4A2 mutations and disease: insights into pathogenic mechanisms and potential therapeutic targets.
    Kuo DS; Labelle-Dumais C; Gould DB
    Hum Mol Genet; 2012 Oct; 21(R1):R97-110. PubMed ID: 22914737
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Elevated TGFβ signaling contributes to cerebral small vessel disease in mouse models of Gould syndrome.
    Branyan K; Labelle-Dumais C; Wang X; Hayashi G; Lee B; Peltz Z; Gorman S; Li BQ; Mao M; Gould DB
    Matrix Biol; 2023 Jan; 115():48-70. PubMed ID: 36435425
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Main features of
    Guey S; Hervé D
    Cereb Circ Cogn Behav; 2022; 3():100140. PubMed ID: 36324412
    [No Abstract]   [Full Text] [Related]  

  • 30. De novo p.G696S mutation in COL4A1 causes intracranial calcification and late-onset cerebral hemorrhage: A case report and review of the literature.
    Kinoshita K; Ishizaki Y; Yamamoto H; Sonoda M; Yonemoto K; Kira R; Sanefuji M; Ueda A; Matsui H; Ando Y; Sakai Y; Ohga S
    Eur J Med Genet; 2020 Apr; 63(4):103825. PubMed ID: 31857254
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Do mutations in COL4A1 or COL4A2 cause thin basement membrane nephropathy (TBMN)?
    Zhang KW; Tonna S; Wang YY; Rana K; Padavarat S; Savige J
    Pediatr Nephrol; 2007 May; 22(5):645-51. PubMed ID: 17216253
    [TBL] [Abstract][Full Text] [Related]  

  • 32. COL4A1 Mutations Cause Neuromuscular Disease with Tissue-Specific Mechanistic Heterogeneity.
    Labelle-Dumais C; Schuitema V; Hayashi G; Hoff K; Gong W; Dao DQ; Ullian EM; Oishi P; Margeta M; Gould DB
    Am J Hum Genet; 2019 May; 104(5):847-860. PubMed ID: 31051113
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Use of sodium 4-phenylbutyrate to define therapeutic parameters for reducing intracerebral hemorrhage and myopathy in
    Hayashi G; Labelle-Dumais C; Gould DB
    Dis Model Mech; 2018 Jul; 11(7):. PubMed ID: 29895609
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Drosophila basement membrane collagen col4a1 mutations cause severe myopathy.
    Kelemen-Valkony I; Kiss M; Csiha J; Kiss A; Bircher U; Szidonya J; Maróy P; Juhász G; Komonyi O; Csiszár K; Mink M
    Matrix Biol; 2012 Jan; 31(1):29-37. PubMed ID: 22037604
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Neurologic phenotypes associated with
    Zagaglia S; Selch C; Nisevic JR; Mei D; Michalak Z; Hernandez-Hernandez L; Krithika S; Vezyroglou K; Varadkar SM; Pepler A; Biskup S; Leão M; Gärtner J; Merkenschlager A; Jaksch M; Møller RS; Gardella E; Kristiansen BS; Hansen LK; Vari MS; Helbig KL; Desai S; Smith-Hicks CL; Hino-Fukuyo N; Talvik T; Laugesaar R; Ilves P; Õunap K; Körber I; Hartlieb T; Kudernatsch M; Winkler P; Schimmel M; Hasse A; Knuf M; Heinemeyer J; Makowski C; Ghedia S; Subramanian GM; Striano P; Thomas RH; Micallef C; Thom M; Werring DJ; Kluger GJ; Cross JH; Guerrini R; Balestrini S; Sisodiya SM
    Neurology; 2018 Nov; 91(22):e2078-e2088. PubMed ID: 30413629
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Fetal brain small vessel disease 1 caused by a novel mutation in the COL4A1 gene.
    England EC; Cornejo P; Neilson DE; Rao RP; Goncalves LF
    Pediatr Radiol; 2021 Mar; 51(3):480-484. PubMed ID: 33057775
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 4-Sodium phenyl butyric acid has both efficacy and counter-indicative effects in the treatment of Col4a1 disease.
    Jones FE; Murray LS; McNeilly S; Dean A; Aman A; Lu Y; Nikolova N; Malomgré R; Horsburgh K; Holmes WM; Kadler KE; Van Agtmael T
    Hum Mol Genet; 2019 Feb; 28(4):628-638. PubMed ID: 30351356
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Prenatal Diagnosis of
    Gubana F; Christov C; Coste T; Tournier-Lasserve E; Benachi A; Fallet-Bianco C; Encha-Razavi F; Martinovic J
    Pediatr Dev Pathol; 2022; 25(4):435-446. PubMed ID: 35382634
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Spectrum of Fetal Intraparenchymal Hemorrhage in COL4A1/A2-Related Disorders.
    George E; Vassar R; Mogga A; Li Y; Norton ME; Gano D; Glenn OA
    Pediatr Neurol; 2023 Oct; 147():63-67. PubMed ID: 37562171
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Coronary-Heart-Disease-Associated Genetic Variant at the COL4A1/COL4A2 Locus Affects COL4A1/COL4A2 Expression, Vascular Cell Survival, Atherosclerotic Plaque Stability and Risk of Myocardial Infarction.
    Yang W; Ng FL; Chan K; Pu X; Poston RN; Ren M; An W; Zhang R; Wu J; Yan S; Situ H; He X; Chen Y; Tan X; Xiao Q; Tucker AT; Caulfield MJ; Ye S
    PLoS Genet; 2016 Jul; 12(7):e1006127. PubMed ID: 27389912
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.