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 *

136 related articles for article (PubMed ID: 19142207)

  • 21. MYO9B gene polymorphisms are associated with autoimmune diseases in Spanish population.
    Sánchez E; Alizadeh BZ; Valdigem G; Ortego-Centeno N; Jiménez-Alonso J; de Ramón E; García A; López-Nevot MA; Wijmenga C; Martín J; Koeleman BP
    Hum Immunol; 2007 Jul; 68(7):610-5. PubMed ID: 17584584
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Is MYO9B the missing link between schizophrenia and celiac disease?
    Jungerius BJ; Bakker SC; Monsuur AJ; Sinke RJ; Kahn RS; Wijmenga C
    Am J Med Genet B Neuropsychiatr Genet; 2008 Apr; 147(3):351-5. PubMed ID: 17948900
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A meta-analysis of the relationship between MYO9B gene polymorphisms and susceptibility to Crohn's disease and ulcerative colitis.
    Li P; Yang XK; Wang X; Zhao MQ; Zhang C; Tao SS; Zhao W; Huang Q; Li LJ; Pan HF; Ye DQ
    Hum Immunol; 2016 Oct; 77(10):990-996. PubMed ID: 27435931
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Replication of genetic variation in the MYO9B gene in Crohn's disease.
    Wolters VM; Xu W; Zhao X; Walters TD; Griffiths AM; Silverberg MS; Muise AM
    Hum Immunol; 2011 Jul; 72(7):592-7. PubMed ID: 21515326
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Frequency of MYO9B polymorphisms in celiac patients and controls.
    Loeff T; Araya M; Pérez-Bravo F
    Rev Esp Enferm Dig; 2012 Dec; 104(11):566-71. PubMed ID: 23368647
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Myosin IXB gene region and gluten intolerance: linkage to coeliac disease and a putative dermatitis herpetiformis association.
    Koskinen LL; Korponay-Szabo IR; Viiri K; Juuti-Uusitalo K; Kaukinen K; Lindfors K; Mustalahti K; Kurppa K; Adány R; Pocsai Z; Széles G; Einarsdottir E; Wijmenga C; Mäki M; Partanen J; Kere J; Saavalainen P
    J Med Genet; 2008 Apr; 45(4):222-7. PubMed ID: 18077767
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Association of Vitamin D Receptor Gene Polymorphisms and the Risk of Multiple Sclerosis: A Meta Analysis.
    Zhang D; Wang L; Zhang R; Li S
    Arch Med Res; 2019 Aug; 50(6):350-361. PubMed ID: 31677540
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The Myosin IXb motor activity targets the myosin IXb RhoGAP domain as cargo to sites of actin polymerization.
    van den Boom F; Düssmann H; Uhlenbrock K; Abouhamed M; Bähler M
    Mol Biol Cell; 2007 Apr; 18(4):1507-18. PubMed ID: 17314409
    [TBL] [Abstract][Full Text] [Related]  

  • 29. IL2RA/CD25 polymorphisms contribute to multiple sclerosis susceptibility.
    Matesanz F; Caro-Maldonado A; Fedetz M; Fernández O; Milne RL; Guerrero M; Delgado C; Alcina A
    J Neurol; 2007 May; 254(5):682-4. PubMed ID: 17420929
    [No Abstract]   [Full Text] [Related]  

  • 30. Aggregation of multiple sclerosis genetic risk variants in multiple and single case families.
    Gourraud PA; McElroy JP; Caillier SJ; Johnson BA; Santaniello A; Hauser SL; Oksenberg JR
    Ann Neurol; 2011 Jan; 69(1):65-74. PubMed ID: 21280076
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Lack of genetic association between the MYO9B locus and schizophrenia in a Chinese population.
    Wang J; Wang Z; Liu Y; Hui L; Du W; Zhao X; Xu Y; Zhang H; Zhao X; Zhang X
    Psychiatr Genet; 2015 Apr; 25(2):97. PubMed ID: 25710847
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A role for myosin IXb, a motor-RhoGAP chimera, in epithelial wound healing and tight junction regulation.
    Chandhoke SK; Mooseker MS
    Mol Biol Cell; 2012 Jul; 23(13):2468-80. PubMed ID: 22573889
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Association analysis of the LAG3 and CD4 genes in multiple sclerosis in two independent populations.
    Lundmark F; Harbo HF; Celius EG; Saarela J; Datta P; Oturai A; Lindgren CM; Masterman T; Salter H; Hillert J
    J Neuroimmunol; 2006 Nov; 180(1-2):193-8. PubMed ID: 17020785
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Closing the case of APOE in multiple sclerosis: no association with disease risk in over 29 000 subjects.
    Lill CM; Liu T; Schjeide BM; Roehr JT; Akkad DA; Damotte V; Alcina A; Ortiz MA; Arroyo R; Lopez de Lapuente A; Blaschke P; Winkelmann A; Gerdes LA; Luessi F; Fernadez O; Izquierdo G; Antigüedad A; Hoffjan S; Cournu-Rebeix I; Gromöller S; Faber H; Liebsch M; Meissner E; Chanvillard C; Touze E; Pico F; Corcia P; ; Dörner T; Steinhagen-Thiessen E; Baeckman L; Heekeren HR; Li SC; Lindenberger U; Chan A; Hartung HP; Aktas O; Lohse P; Kümpfel T; Kubisch C; Epplen JT; Zettl UK; Fontaine B; Vandenbroeck K; Matesanz F; Urcelay E; Bertram L; Zipp F
    J Med Genet; 2012 Sep; 49(9):558-62. PubMed ID: 22972946
    [TBL] [Abstract][Full Text] [Related]  

  • 35. No evidence for association of multiple sclerosis with the complement factors C6 and C7.
    Chataway J; Sawcer S; Sherman D; Hobart M; Fernie B; Coraddu F; Feakes R; Broadley S; Gray J; Jones HB; Clayton D; Goodfellow PN; Compston A
    J Neuroimmunol; 1999 Sep; 99(1):150-6. PubMed ID: 10496188
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Multiple sclerosis association study with the TENR-IL2-IL21 region in a Spanish population.
    Fedetz M; Ndagire D; Fernandez O; Leyva L; Guerrero M; Arnal C; Lucas M; Izquierdo G; Delgado C; Alcina A; Matesanz F
    Tissue Antigens; 2009 Sep; 74(3):244-7. PubMed ID: 19523143
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The autoimmune disease-associated KIF5A, CD226 and SH2B3 gene variants confer susceptibility for multiple sclerosis.
    Alcina A; Vandenbroeck K; Otaegui D; Saiz A; Gonzalez JR; Fernandez O; Cavanillas ML; Cénit MC; Arroyo R; Alloza I; García-Barcina M; Antigüedad A; Leyva L; Izquierdo G; Lucas M; Fedetz M; Pinto-Medel MJ; Olascoaga J; Blanco Y; Comabella M; Montalban X; Urcelay E; Matesanz F
    Genes Immun; 2010 Jul; 11(5):439-45. PubMed ID: 20508602
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Multiple sclerosis: the increased frequency of the ICAM-1 exon 6 gene point mutation genetic type K469.
    Mycko MP; Kwinkowski M; Tronczynska E; Szymanska B; Selmaj KW
    Ann Neurol; 1998 Jul; 44(1):70-5. PubMed ID: 9667594
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Motorized RhoGAP myosin IXb (Myo9b) controls cell shape and motility.
    Hanley PJ; Xu Y; Kronlage M; Grobe K; Schön P; Song J; Sorokin L; Schwab A; Bähler M
    Proc Natl Acad Sci U S A; 2010 Jul; 107(27):12145-50. PubMed ID: 20566876
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Identification of 11 novel and common single nucleotide polymorphisms in the interleukin-7 receptor-alpha gene and their associations with multiple sclerosis.
    Teutsch SM; Booth DR; Bennetts BH; Heard RN; Stewart GJ
    Eur J Hum Genet; 2003 Jul; 11(7):509-15. PubMed ID: 12825072
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.