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 *

200 related articles for article (PubMed ID: 9811928)

  • 21. A locus for cerebral cavernous malformations maps to chromosome 7q in two families.
    Marchuk DA; Gallione CJ; Morrison LA; Clericuzio CL; Hart BL; Kosofsky BE; Louis DN; Gusella JF; Davis LE; Prenger VL
    Genomics; 1995 Jul; 28(2):311-4. PubMed ID: 8530042
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35.
    Hocking LJ; Herbert CA; Nicholls RK; Williams F; Bennett ST; Cundy T; Nicholson GC; Wuyts W; Van Hul W; Ralston SH
    Am J Hum Genet; 2001 Nov; 69(5):1055-61. PubMed ID: 11555792
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Genetic heterogeneity and absence of founder effect in a series of 36 French cerebral cavernous angiomas families.
    Laberge S; Labauge P; Maréchal E; Maciazek J; Tournier-Lasserve E
    Eur J Hum Genet; 1999; 7(4):499-504. PubMed ID: 10352941
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Familial cavernous malformations of the central nervous system. A clinical and genetic study of 15 German families].
    Siegel AM; Bertalanffy H; Dichgans JJ; Elger CE; Hopf H; Hopf N; Keidel M; Kleider A; Nowak G; Pfeiffer RA; Schramm J; Spuck S; Stefan H; Sure U; Baumann CR; Rouleau GA; Verlaan DJ; Andermann E; Andermann F
    Nervenarzt; 2005 Feb; 76(2):175-80. PubMed ID: 15702360
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Spectrum of genotype and clinical manifestations in cerebral cavernous malformations.
    Gault J; Sain S; Hu LJ; Awad IA
    Neurosurgery; 2006 Dec; 59(6):1278-84; discussion 1284-5. PubMed ID: 17277691
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A major locus for myoclonus-dystonia maps to chromosome 7q in eight families.
    Klein C; Schilling K; Saunders-Pullman RJ; Garrels J; Breakefield XO; Brin MF; deLeon D; Doheny D; Fahn S; Fink JS; Forsgren L; Friedman J; Frucht S; Harris J; Holmgren G; Kis B; Kurlan R; Kyllerman M; Lang AE; Leung J; Raymond D; Robishaw JD; Sanner G; Schwinger E; Tabamo RE; Tagliati M
    Am J Hum Genet; 2000 Nov; 67(5):1314-9. PubMed ID: 11022010
    [TBL] [Abstract][Full Text] [Related]  

  • 27. CCM1 gene mutations in families segregating cerebral cavernous malformations.
    Davenport WJ; Siegel AM; Dichgans J; Drigo P; Mammi I; Pereda P; Wood NW; Rouleau GA
    Neurology; 2001 Feb; 56(4):540-3. PubMed ID: 11222804
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genomic causes of multiple cerebral cavernous malformations in a Japanese population.
    Tsutsumi S; Ogino I; Miyajima M; Ikeda T; Shindo N; Yasumoto Y; Ito M; Arai H
    J Clin Neurosci; 2013 May; 20(5):667-9. PubMed ID: 23485406
    [TBL] [Abstract][Full Text] [Related]  

  • 29. First interchromosomal insertion in a patient with cerebral and spinal cavernous malformations.
    Pilz RA; Schwefel K; Weise A; Liehr T; Demmer P; Spuler A; Spiegler S; Gilberg E; Hübner CA; Felbor U; Rath M
    Sci Rep; 2020 Apr; 10(1):6306. PubMed ID: 32286434
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Cerebral cavernous malformation: new molecular and clinical insights.
    Revencu N; Vikkula M
    J Med Genet; 2006 Sep; 43(9):716-21. PubMed ID: 16571644
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A Novel CCM1/KRIT1 Heterozygous Nonsense Mutation (c.1864C>T) Associated with Familial Cerebral Cavernous Malformation: a Genetic Insight from an 8-Year Continuous Observational Study.
    Yang C; Nicholas VH; Zhao J; Wu B; Zhong H; Li Y; Xu Y
    J Mol Neurosci; 2017 Apr; 61(4):511-523. PubMed ID: 28255959
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Genome-wide linkage analysis reveals evidence for four new susceptibility loci for familial euthyroid goiter.
    Bayer Y; Neumann S; Meyer B; Rüschendorf F; Reske A; Brix T; Hegedüs L; Langer P; Nürnberg P; Paschke R
    J Clin Endocrinol Metab; 2004 Aug; 89(8):4044-52. PubMed ID: 15292347
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Identification of a Novel Deletion Mutation (c.1780delG) and a Novel Splice-Site Mutation (c.1412-1G>A) in the CCM1/KRIT1 Gene Associated with Familial Cerebral Cavernous Malformation in the Chinese Population.
    Yang C; Zhao J; Wu B; Zhong H; Li Y; Xu Y
    J Mol Neurosci; 2017 Jan; 61(1):8-15. PubMed ID: 27649701
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Significant evidence of one or more susceptibility loci for endometriosis with near-Mendelian inheritance on chromosome 7p13-15.
    Zondervan KT; Treloar SA; Lin J; Weeks DE; Nyholt DR; Mangion J; MacKay IJ; Cardon LR; Martin NG; Kennedy SH; Montgomery GW
    Hum Reprod; 2007 Mar; 22(3):717-28. PubMed ID: 17158817
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Loss of p53 sensitizes mice with a mutation in Ccm1 (KRIT1) to development of cerebral vascular malformations.
    Plummer NW; Gallione CJ; Srinivasan S; Zawistowski JS; Louis DN; Marchuk DA
    Am J Pathol; 2004 Nov; 165(5):1509-18. PubMed ID: 15509522
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Model-based linkage analyses confirm chromosome 19q13.3 as a susceptibility locus for intracranial aneurysm.
    Mineharu Y; Inoue K; Inoue S; Yamada S; Nozaki K; Hashimoto N; Koizumi A
    Stroke; 2007 Apr; 38(4):1174-8. PubMed ID: 17322081
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Differential angiogenesis function of CCM2 and CCM3 in cerebral cavernous malformations.
    Zhu Y; Wu Q; Xu JF; Miller D; Sandalcioglu IE; Zhang JM; Sure U
    Neurosurg Focus; 2010 Sep; 29(3):E1. PubMed ID: 20809750
    [TBL] [Abstract][Full Text] [Related]  

  • 38. High-throughput sequencing of the entire genomic regions of CCM1/KRIT1, CCM2 and CCM3/PDCD10 to search for pathogenic deep-intronic splice mutations in cerebral cavernous malformations.
    Rath M; Jenssen SE; Schwefel K; Spiegler S; Kleimeier D; Sperling C; Kaderali L; Felbor U
    Eur J Med Genet; 2017 Sep; 60(9):479-484. PubMed ID: 28645800
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1).
    Sahoo T; Johnson EW; Thomas JW; Kuehl PM; Jones TL; Dokken CG; Touchman JW; Gallione CJ; Lee-Lin SQ; Kosofsky B; Kurth JH; Louis DN; Mettler G; Morrison L; Gil-Nagel A; Rich SS; Zabramski JM; Boguski MS; Green ED; Marchuk DA
    Hum Mol Genet; 1999 Nov; 8(12):2325-33. PubMed ID: 10545614
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A gene responsible for cavernous malformations of the brain maps to chromosome 7q.
    Dubovsky J; Zabramski JM; Kurth J; Spetzler RF; Rich SS; Orr HT; Weber JL
    Hum Mol Genet; 1995 Mar; 4(3):453-8. PubMed ID: 7795602
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.