BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

552 related articles for article (PubMed ID: 12690205)

  • 1. Human chromosome 7: DNA sequence and biology.
    Scherer SW; Cheung J; MacDonald JR; Osborne LR; Nakabayashi K; Herbrick JA; Carson AR; Parker-Katiraee L; Skaug J; Khaja R; Zhang J; Hudek AK; Li M; Haddad M; Duggan GE; Fernandez BA; Kanematsu E; Gentles S; Christopoulos CC; Choufani S; Kwasnicka D; Zheng XH; Lai Z; Nusskern D; Zhang Q; Gu Z; Lu F; Zeesman S; Nowaczyk MJ; Teshima I; Chitayat D; Shuman C; Weksberg R; Zackai EH; Grebe TA; Cox SR; Kirkpatrick SJ; Rahman N; Friedman JM; Heng HH; Pelicci PG; Lo-Coco F; Belloni E; Shaffer LG; Pober B; Morton CC; Gusella JF; Bruns GA; Korf BR; Quade BJ; Ligon AH; Ferguson H; Higgins AW; Leach NT; Herrick SR; Lemyre E; Farra CG; Kim HG; Summers AM; Gripp KW; Roberts W; Szatmari P; Winsor EJ; Grzeschik KH; Teebi A; Minassian BA; Kere J; Armengol L; Pujana MA; Estivill X; Wilson MD; Koop BF; Tosi S; Moore GE; Boright AP; Zlotorynski E; Kerem B; Kroisel PM; Petek E; Oscier DG; Mould SJ; Döhner H; Döhner K; Rommens JM; Vincent JB; Venter JC; Li PW; Mural RJ; Adams MD; Tsui LC
    Science; 2003 May; 300(5620):767-72. PubMed ID: 12690205
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Generation and annotation of the DNA sequences of human chromosomes 2 and 4.
    Hillier LW; Graves TA; Fulton RS; Fulton LA; Pepin KH; Minx P; Wagner-McPherson C; Layman D; Wylie K; Sekhon M; Becker MC; Fewell GA; Delehaunty KD; Miner TL; Nash WE; Kremitzki C; Oddy L; Du H; Sun H; Bradshaw-Cordum H; Ali J; Carter J; Cordes M; Harris A; Isak A; van Brunt A; Nguyen C; Du F; Courtney L; Kalicki J; Ozersky P; Abbott S; Armstrong J; Belter EA; Caruso L; Cedroni M; Cotton M; Davidson T; Desai A; Elliott G; Erb T; Fronick C; Gaige T; Haakenson W; Haglund K; Holmes A; Harkins R; Kim K; Kruchowski SS; Strong CM; Grewal N; Goyea E; Hou S; Levy A; Martinka S; Mead K; McLellan MD; Meyer R; Randall-Maher J; Tomlinson C; Dauphin-Kohlberg S; Kozlowicz-Reilly A; Shah N; Swearengen-Shahid S; Snider J; Strong JT; Thompson J; Yoakum M; Leonard S; Pearman C; Trani L; Radionenko M; Waligorski JE; Wang C; Rock SM; Tin-Wollam AM; Maupin R; Latreille P; Wendl MC; Yang SP; Pohl C; Wallis JW; Spieth J; Bieri TA; Berkowicz N; Nelson JO; Osborne J; Ding L; Meyer R; Sabo A; Shotland Y; Sinha P; Wohldmann PE; Cook LL; Hickenbotham MT; Eldred J; Williams D; Jones TA; She X; Ciccarelli FD; Izaurralde E; Taylor J; Schmutz J; Myers RM; Cox DR; Huang X; McPherson JD; Mardis ER; Clifton SW; Warren WC; Chinwalla AT; Eddy SR; Marra MA; Ovcharenko I; Furey TS; Miller W; Eichler EE; Bork P; Suyama M; Torrents D; Waterston RH; Wilson RK
    Nature; 2005 Apr; 434(7034):724-31. PubMed ID: 15815621
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: the low-copy repeats that flank the Williams-Beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s).
    Valero MC; de Luis O; Cruces J; Pérez Jurado LA
    Genomics; 2000 Oct; 69(1):1-13. PubMed ID: 11013070
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The DNA sequence of human chromosome 7.
    Hillier LW; Fulton RS; Fulton LA; Graves TA; Pepin KH; Wagner-McPherson C; Layman D; Maas J; Jaeger S; Walker R; Wylie K; Sekhon M; Becker MC; O'Laughlin MD; Schaller ME; Fewell GA; Delehaunty KD; Miner TL; Nash WE; Cordes M; Du H; Sun H; Edwards J; Bradshaw-Cordum H; Ali J; Andrews S; Isak A; Vanbrunt A; Nguyen C; Du F; Lamar B; Courtney L; Kalicki J; Ozersky P; Bielicki L; Scott K; Holmes A; Harkins R; Harris A; Strong CM; Hou S; Tomlinson C; Dauphin-Kohlberg S; Kozlowicz-Reilly A; Leonard S; Rohlfing T; Rock SM; Tin-Wollam AM; Abbott A; Minx P; Maupin R; Strowmatt C; Latreille P; Miller N; Johnson D; Murray J; Woessner JP; Wendl MC; Yang SP; Schultz BR; Wallis JW; Spieth J; Bieri TA; Nelson JO; Berkowicz N; Wohldmann PE; Cook LL; Hickenbotham MT; Eldred J; Williams D; Bedell JA; Mardis ER; Clifton SW; Chissoe SL; Marra MA; Raymond C; Haugen E; Gillett W; Zhou Y; James R; Phelps K; Iadanoto S; Bubb K; Simms E; Levy R; Clendenning J; Kaul R; Kent WJ; Furey TS; Baertsch RA; Brent MR; Keibler E; Flicek P; Bork P; Suyama M; Bailey JA; Portnoy ME; Torrents D; Chinwalla AT; Gish WR; Eddy SR; McPherson JD; Olson MV; Eichler EE; Green ED; Waterston RH; Wilson RK
    Nature; 2003 Jul; 424(6945):157-64. PubMed ID: 12853948
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of the human/mouse syntenic common fragile site FRA7K/Fra12C1--relation of FRA7K and other human common fragile sites on chromosome 7 to evolutionary breakpoints.
    Helmrich A; Stout-Weider K; Matthaei A; Hermann K; Heiden T; Schrock E
    Int J Cancer; 2007 Jan; 120(1):48-54. PubMed ID: 17039484
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Juxtacentromeric region of human chromosome 21: a boundary between centromeric heterochromatin and euchromatic chromosome arms.
    Brun ME; Ruault M; Ventura M; Roizès G; De Sario A
    Gene; 2003 Jul; 312():41-50. PubMed ID: 12909339
    [TBL] [Abstract][Full Text] [Related]  

  • 7. PMS2-related genes flank the rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7.
    Osborne LR; Herbrick JA; Greavette T; Heng HH; Tsui LC; Scherer SW
    Genomics; 1997 Oct; 45(2):402-6. PubMed ID: 9344666
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Characterization of FRA7B, a human common fragile site mapped at the 7p chromosome terminal region.
    Bosco N; Pelliccia F; Rocchi A
    Cancer Genet Cytogenet; 2010 Oct; 202(1):47-52. PubMed ID: 20804921
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Duplication of the Williams-Beuren critical region: case report and further delineation of the phenotypic spectrum.
    Orellana C; Bernabeu J; Monfort S; Roselló M; Oltra S; Ferrer I; Quiroga R; Martínez-Garay I; Martínez F
    J Med Genet; 2008 Mar; 45(3):187-9. PubMed ID: 18310268
    [No Abstract]   [Full Text] [Related]  

  • 10. Characterization of the human TESTIN gene localized in the FRA7G region at 7q31.2.
    Tatarelli C; Linnenbach A; Mimori K; Croce CM
    Genomics; 2000 Aug; 68(1):1-12. PubMed ID: 10950921
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Comparative mapping of the region of human chromosome 7 deleted in williams syndrome.
    DeSilva U; Massa H; Trask BJ; Green ED
    Genome Res; 1999 May; 9(5):428-36. PubMed ID: 10330122
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The murine CYLN2 gene: genomic organization, chromosome localization, and comparison to the human gene that is located within the 7q11.23 Williams syndrome critical region.
    Hoogenraad CC; Eussen BH; Langeveld A; van Haperen R; Winterberg S; Wouters CH; Grosveld F; De Zeeuw CI; Galjart N
    Genomics; 1998 Nov; 53(3):348-58. PubMed ID: 9799601
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Autism and Williams syndrome: a case report.
    Herguner S; Mukaddes NM
    World J Biol Psychiatry; 2006; 7(3):186-8. PubMed ID: 16861145
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Copy number variation in regions flanked (or unflanked) by duplicons among patients with developmental delay and/or congenital malformations; detection of reciprocal and partial Williams-Beuren duplications.
    Kriek M; White SJ; Szuhai K; Knijnenburg J; van Ommen GJ; den Dunnen JT; Breuning MH
    Eur J Hum Genet; 2006 Feb; 14(2):180-9. PubMed ID: 16391556
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The sequence of the human genome.
    Venter JC; Adams MD; Myers EW; Li PW; Mural RJ; Sutton GG; Smith HO; Yandell M; Evans CA; Holt RA; Gocayne JD; Amanatides P; Ballew RM; Huson DH; Wortman JR; Zhang Q; Kodira CD; Zheng XH; Chen L; Skupski M; Subramanian G; Thomas PD; Zhang J; Gabor Miklos GL; Nelson C; Broder S; Clark AG; Nadeau J; McKusick VA; Zinder N; Levine AJ; Roberts RJ; Simon M; Slayman C; Hunkapiller M; Bolanos R; Delcher A; Dew I; Fasulo D; Flanigan M; Florea L; Halpern A; Hannenhalli S; Kravitz S; Levy S; Mobarry C; Reinert K; Remington K; Abu-Threideh J; Beasley E; Biddick K; Bonazzi V; Brandon R; Cargill M; Chandramouliswaran I; Charlab R; Chaturvedi K; Deng Z; Di Francesco V; Dunn P; Eilbeck K; Evangelista C; Gabrielian AE; Gan W; Ge W; Gong F; Gu Z; Guan P; Heiman TJ; Higgins ME; Ji RR; Ke Z; Ketchum KA; Lai Z; Lei Y; Li Z; Li J; Liang Y; Lin X; Lu F; Merkulov GV; Milshina N; Moore HM; Naik AK; Narayan VA; Neelam B; Nusskern D; Rusch DB; Salzberg S; Shao W; Shue B; Sun J; Wang Z; Wang A; Wang X; Wang J; Wei M; Wides R; Xiao C; Yan C; Yao A; Ye J; Zhan M; Zhang W; Zhang H; Zhao Q; Zheng L; Zhong F; Zhong W; Zhu S; Zhao S; Gilbert D; Baumhueter S; Spier G; Carter C; Cravchik A; Woodage T; Ali F; An H; Awe A; Baldwin D; Baden H; Barnstead M; Barrow I; Beeson K; Busam D; Carver A; Center A; Cheng ML; Curry L; Danaher S; Davenport L; Desilets R; Dietz S; Dodson K; Doup L; Ferriera S; Garg N; Gluecksmann A; Hart B; Haynes J; Haynes C; Heiner C; Hladun S; Hostin D; Houck J; Howland T; Ibegwam C; Johnson J; Kalush F; Kline L; Koduru S; Love A; Mann F; May D; McCawley S; McIntosh T; McMullen I; Moy M; Moy L; Murphy B; Nelson K; Pfannkoch C; Pratts E; Puri V; Qureshi H; Reardon M; Rodriguez R; Rogers YH; Romblad D; Ruhfel B; Scott R; Sitter C; Smallwood M; Stewart E; Strong R; Suh E; Thomas R; Tint NN; Tse S; Vech C; Wang G; Wetter J; Williams S; Williams M; Windsor S; Winn-Deen E; Wolfe K; Zaveri J; Zaveri K; Abril JF; Guigó R; Campbell MJ; Sjolander KV; Karlak B; Kejariwal A; Mi H; Lazareva B; Hatton T; Narechania A; Diemer K; Muruganujan A; Guo N; Sato S; Bafna V; Istrail S; Lippert R; Schwartz R; Walenz B; Yooseph S; Allen D; Basu A; Baxendale J; Blick L; Caminha M; Carnes-Stine J; Caulk P; Chiang YH; Coyne M; Dahlke C; Deslattes Mays A; Dombroski M; Donnelly M; Ely D; Esparham S; Fosler C; Gire H; Glanowski S; Glasser K; Glodek A; Gorokhov M; Graham K; Gropman B; Harris M; Heil J; Henderson S; Hoover J; Jennings D; Jordan C; Jordan J; Kasha J; Kagan L; Kraft C; Levitsky A; Lewis M; Liu X; Lopez J; Ma D; Majoros W; McDaniel J; Murphy S; Newman M; Nguyen T; Nguyen N; Nodell M; Pan S; Peck J; Peterson M; Rowe W; Sanders R; Scott J; Simpson M; Smith T; Sprague A; Stockwell T; Turner R; Venter E; Wang M; Wen M; Wu D; Wu M; Xia A; Zandieh A; Zhu X
    Science; 2001 Feb; 291(5507):1304-51. PubMed ID: 11181995
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The DNA sequence and biology of human chromosome 19.
    Grimwood J; Gordon LA; Olsen A; Terry A; Schmutz J; Lamerdin J; Hellsten U; Goodstein D; Couronne O; Tran-Gyamfi M; Aerts A; Altherr M; Ashworth L; Bajorek E; Black S; Branscomb E; Caenepeel S; Carrano A; Caoile C; Chan YM; Christensen M; Cleland CA; Copeland A; Dalin E; Dehal P; Denys M; Detter JC; Escobar J; Flowers D; Fotopulos D; Garcia C; Georgescu AM; Glavina T; Gomez M; Gonzales E; Groza M; Hammon N; Hawkins T; Haydu L; Ho I; Huang W; Israni S; Jett J; Kadner K; Kimball H; Kobayashi A; Larionov V; Leem SH; Lopez F; Lou Y; Lowry S; Malfatti S; Martinez D; McCready P; Medina C; Morgan J; Nelson K; Nolan M; Ovcharenko I; Pitluck S; Pollard M; Popkie AP; Predki P; Quan G; Ramirez L; Rash S; Retterer J; Rodriguez A; Rogers S; Salamov A; Salazar A; She X; Smith D; Slezak T; Solovyev V; Thayer N; Tice H; Tsai M; Ustaszewska A; Vo N; Wagner M; Wheeler J; Wu K; Xie G; Yang J; Dubchak I; Furey TS; DeJong P; Dickson M; Gordon D; Eichler EE; Pennacchio LA; Richardson P; Stubbs L; Rokhsar DS; Myers RM; Rubin EM; Lucas SM
    Nature; 2004 Apr; 428(6982):529-35. PubMed ID: 15057824
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular genetic studies of human chromosome 7 in Russell-Silver syndrome.
    Nakabayashi K; Fernandez BA; Teshima I; Shuman C; Proud VK; Curry CJ; Chitayat D; Grebe T; Ming J; Oshimura M; Meguro M; Mitsuya K; Deb-Rinker P; Herbrick JA; Weksberg R; Scherer SW
    Genomics; 2002 Feb; 79(2):186-96. PubMed ID: 11829489
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome.
    DeSilva U; Elnitski L; Idol JR; Doyle JL; Gan W; Thomas JW; Schwartz S; Dietrich NL; Beckstrom-Sternberg SM; McDowell JC; Blakesley RW; Bouffard GG; Thomas PJ; Touchman JW; Miller W; Green ED
    Genome Res; 2002 Jan; 12(1):3-15. PubMed ID: 11779826
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cloning and characterization of the common fragile site FRA6F harboring a replicative senescence gene and frequently deleted in human tumors.
    Morelli C; Karayianni E; Magnanini C; Mungall AJ; Thorland E; Negrini M; Smith DI; Barbanti-Brodano G
    Oncogene; 2002 Oct; 21(47):7266-76. PubMed ID: 12370818
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region.
    Bonora E; Bacchelli E; Levy ER; Blasi F; Marlow A; Monaco AP; Maestrini E;
    Mol Psychiatry; 2002; 7(3):289-301. PubMed ID: 11920156
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 28.