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 *

207 related articles for article (PubMed ID: 9811928)

  • 1. Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27.
    Craig HD; Günel M; Cepeda O; Johnson EW; Ptacek L; Steinberg GK; Ogilvy CS; Berg MJ; Crawford SC; Scott RM; Steichen-Gersdorf E; Sabroe R; Kennedy CT; Mettler G; Beis MJ; Fryer A; Awad IA; Lifton RP
    Hum Mol Genet; 1998 Nov; 7(12):1851-8. PubMed ID: 9811928
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Linkage to the CCM2 locus and genetic heterogeneity in familial cerebral cavernous malformation.
    Dupré N; Verlaan DJ; Hand CK; Laurent SB; Turecki G; Davenport WJ; Acciarri N; Dichgans J; Ohkuma A; Siegel AM; Rouleau GA
    Can J Neurol Sci; 2003 May; 30(2):122-8. PubMed ID: 12774951
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Refined localization of the cerebral cavernous malformation gene (CCM1) to a 4-cM interval of chromosome 7q contained in a well-defined YAC contig.
    Johnson EW; Iyer LM; Rich SS; Orr HT; Gil-Nagel A; Kurth JH; Zabramski JM; Marchuk DA; Weissenbach J; Clericuzio CL; Davis LE; Hart BL; Gusella JF; Kosofsky BE; Louis DN; Morrison LA; Green ED; Weber JL
    Genome Res; 1995 Nov; 5(4):368-80. PubMed ID: 8750196
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic heterogeneity of inherited cerebral cavernous malformation.
    Günel M; Awad IA; Finberg K; Steinberg GK; Craig HD; Cepeda O; Nelson-Williams C; Lifton RP
    Neurosurgery; 1996 Jun; 38(6):1265-71. PubMed ID: 8727164
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutational analysis of 206 families with cavernous malformations.
    Laurans MS; DiLuna ML; Shin D; Niazi F; Voorhees JR; Nelson-Williams C; Johnson EW; Siegel AM; Steinberg GK; Berg MJ; Scott RM; Tedeschi G; Enevoldson TP; Anson J; Rouleau GA; Ogilvy C; Awad IA; Lifton RP; Gunel M
    J Neurosurg; 2003 Jul; 99(1):38-43. PubMed ID: 12854741
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Linkage of the locus for cerebral cavernous hemangiomas to human chromosome 7q in four families of Mexican-American descent.
    Polymeropoulos MH; Hurko O; Hsu F; Rubenstein J; Basnet S; Lane K; Dietz H; Spetzler RF; Rigamonti D
    Neurology; 1997 Mar; 48(3):752-7. PubMed ID: 9065560
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A founder mutation as a cause of cerebral cavernous malformation in Hispanic Americans.
    Gunel M; Awad IA; Finberg K; Anson JA; Steinberg GK; Batjer HH; Kopitnik TA; Morrison L; Giannotta SL; Nelson-Williams C; Lifton RP
    N Engl J Med; 1996 Apr; 334(15):946-51. PubMed ID: 8596595
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Familial cavernous malformations in a large French kindred: mapping of the gene to the CCM1 locus on chromosome 7q.
    Notelet L; Chapon F; Khoury S; Vahedi K; Chodkiewicz JP; Courtheoux P; Iba-Zizen MT; Cabanis EA; Lechevalier B; Tournier-Lasserve E; Houtteville JP
    J Neurol Neurosurg Psychiatry; 1997 Jul; 63(1):40-5. PubMed ID: 9221966
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mapping a gene causing cerebral cavernous malformation to 7q11.2-q21.
    Günel M; Awad IA; Anson J; Lifton RP
    Proc Natl Acad Sci U S A; 1995 Jul; 92(14):6620-4. PubMed ID: 7604043
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Inherited cavernous malformations of the central nervous system: clinical and genetic features in 19 Swiss families.
    Graeni C; Stepper F; Sturzenegger M; Merlo A; Verlaan DJ; Andermann F; Baumann CR; Bonassin F; Georgiadis D; Baumgartner RW; Rouleau GA; Siegel AM
    Neurosurg Rev; 2010 Jan; 33(1):47-51. PubMed ID: 19760287
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical, magnetic resonance imaging, and genetic study of 5 Italian families with cerebral cavernous malformation.
    Battistini S; Rocchi R; Cerase A; Citterio A; Tassi L; Lando G; Patrosso MC; Galli R; Brunori P; Sgrò DL; Pitillo G; Lo Russo G; Marocchi A; Penco S
    Arch Neurol; 2007 Jun; 64(6):843-8. PubMed ID: 17562932
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Low frequency of PDCD10 mutations in a panel of CCM3 probands: potential for a fourth CCM locus.
    Liquori CL; Berg MJ; Squitieri F; Ottenbacher M; Sorlie M; Leedom TP; Cannella M; Maglione V; Ptacek L; Johnson EW; Marchuk DA
    Hum Mutat; 2006 Jan; 27(1):118. PubMed ID: 16329096
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Cerebral cavernous malformation--its genetic and biological background].
    Fujimura M; Tominaga T
    Brain Nerve; 2008 Nov; 60(11):1271-4. PubMed ID: 19069160
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Cerebral cavernous malformations].
    Koht J; Braathen GJ; Neubert D; Russell MB
    Tidsskr Nor Laegeforen; 2005 Aug; 125(15):2008-10. PubMed ID: 16100539
    [TBL] [Abstract][Full Text] [Related]  

  • 15. CCM3 mutations are uncommon in cerebral cavernous malformations.
    Verlaan DJ; Roussel J; Laurent SB; Elger CE; Siegel AM; Rouleau GA
    Neurology; 2005 Dec; 65(12):1982-3. PubMed ID: 16380626
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A new locus for familial temporal lobe epilepsy on chromosome 3q.
    Chahine L; Abou-Khalil B; Siren A; Andermann F; Hedera P; Ge Q; Andermann E; Pandolfo M
    Epilepsy Res; 2013 Oct; 106(3):338-44. PubMed ID: 24021842
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutations within the MGC4607 gene cause cerebral cavernous malformations.
    Denier C; Goutagny S; Labauge P; Krivosic V; Arnoult M; Cousin A; Benabid AL; Comoy J; Frerebeau P; Gilbert B; Houtteville JP; Jan M; Lapierre F; Loiseau H; Menei P; Mercier P; Moreau JJ; Nivelon-Chevallier A; Parker F; Redondo AM; Scarabin JM; Tremoulet M; Zerah M; Maciazek J; Tournier-Lasserve E;
    Am J Hum Genet; 2004 Feb; 74(2):326-37. PubMed ID: 14740320
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of a c.601C>G mutation in the CCM1 gene in a kindred with multiple skin, spinal and cerebral cavernous malformations.
    Haghighi A; Fathi D; Shahbazi M; Motahari MM; Friedman B
    J Neurol Sci; 2013 Nov; 334(1-2):97-101. PubMed ID: 24007869
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel CCM1, CCM2, and CCM3 mutations in patients with cerebral cavernous malformations: in-frame deletion in CCM2 prevents formation of a CCM1/CCM2/CCM3 protein complex.
    Stahl S; Gaetzner S; Voss K; Brackertz B; Schleider E; Sürücü O; Kunze E; Netzer C; Korenke C; Finckh U; Habek M; Poljakovic Z; Elbracht M; Rudnik-Schöneborn S; Bertalanffy H; Sure U; Felbor U
    Hum Mutat; 2008 May; 29(5):709-17. PubMed ID: 18300272
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic linkage mapping for a susceptibility locus to bipolar illness: chromosomes 2, 3, 4, 7, 9, 10p, 11p, 22, and Xpter.
    Detera-Wadleigh SD; Hsieh WT; Berrettini WH; Goldin LR; Rollins DY; Muniec D; Grewal R; Guroff JJ; Turner G; Coffman D
    Am J Med Genet; 1994 Sep; 54(3):206-18. PubMed ID: 7810578
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.