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    Results: 1 to 20 of 30

    1.

    The DNA sequence, annotation and analysis of human chromosome 3.

    Muzny DM, Scherer SE, Kaul R, Wang J, Yu J, Sudbrak R, Buhay CJ, Chen R, Cree A, Ding Y, Dugan-Rocha S, Gill R, Gunaratne P, Harris RA, Hawes AC, Hernandez J, Hodgson AV, Hume J, Jackson A, Khan ZM, Kovar-Smith C, Lewis LR, Lozado RJ, Metzker ML, Milosavljevic A, Miner GR, Morgan MB, Nazareth LV, Scott G, Sodergren E, Song XZ, Steffen D, Wei S, Wheeler DA, Wright MW, Worley KC, Yuan Y, Zhang Z, Adams CQ, Ansari-Lari MA, Ayele M, Brown MJ, Chen G, Chen Z, Clendenning J, Clerc-Blankenburg KP, Chen R, Chen Z, Davis C, Delgado O, Dinh HH, Dong W, Draper H, Ernst S, Fu G, Gonzalez-Garay ML, Garcia DK, Gillett W, Gu J, Hao B, Haugen E, Havlak P, He X, Hennig S, Hu S, Huang W, Jackson LR, Jacob LS, Kelly SH, Kube M, Levy R, Li Z, Liu B, Liu J, Liu W, Lu J, Maheshwari M, Nguyen BV, Okwuonu GO, Palmeiri A, Pasternak S, Perez LM, Phelps KA, Plopper FJ, Qiang B, Raymond C, Rodriguez R, Saenphimmachak C, Santibanez J, Shen H, Shen Y, Subramanian S, Tabor PE, Verduzco D, Waldron L, Wang J, Wang J, Wang Q, Williams GA, Wong GK, Yao Z, Zhang J, Zhang X, Zhao G, Zhou J, Zhou Y, Nelson D, Lehrach H, Reinhardt R, Naylor SL, Yang H, Olson M, Weinstock G, Gibbs RA.

    Nature. 2006 Apr 27;440(7088):1194-8.PMID: 16641997 [PubMed - indexed for MEDLINE]Related articles

    2.

    DNAH5 mutations are a common cause of primary ciliary dyskinesia with outer dynein arm defects.

    Hornef N, Olbrich H, Horvath J, Zariwala MA, Fliegauf M, Loges NT, Wildhaber J, Noone PG, Kennedy M, Antonarakis SE, Blouin JL, Bartoloni L, Nüsslein T, Ahrens P, Griese M, Kuhl H, Sudbrak R, Knowles MR, Reinhardt R, Omran H.

    Am J Respir Crit Care Med. 2006 Jul 15;174(2):120-6. Epub 2006 Apr 20.PMID: 16627867 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    Identification and analysis of axonemal dynein light chain 1 in primary ciliary dyskinesia patients.

    Horváth J, Fliegauf M, Olbrich H, Kispert A, King SM, Mitchison H, Zariwala MA, Knowles MR, Sudbrak R, Fekete G, Neesen J, Reinhardt R, Omran H.

    Am J Respir Cell Mol Biol. 2005 Jul;33(1):41-7. Epub 2005 Apr 21.PMID: 15845866 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    Mutational analysis of the NPHP4 gene in 250 patients with nephronophthisis.

    Hoefele J, Sudbrak R, Reinhardt R, Lehrack S, Hennig S, Imm A, Muerb U, Utsch B, Attanasio M, O'Toole JF, Otto E, Hildebrandt F.

    Hum Mutat. 2005 Apr;25(4):411.PMID: 15776426 [PubMed - indexed for MEDLINE]Related articles

    5.

    The DNA sequence of the human X chromosome.

    Ross MT, Grafham DV, Coffey AJ, Scherer S, McLay K, Muzny D, Platzer M, Howell GR, Burrows C, Bird CP, Frankish A, Lovell FL, Howe KL, Ashurst JL, Fulton RS, Sudbrak R, Wen G, Jones MC, Hurles ME, Andrews TD, Scott CE, Searle S, Ramser J, Whittaker A, Deadman R, Carter NP, Hunt SE, Chen R, Cree A, Gunaratne P, Havlak P, Hodgson A, Metzker ML, Richards S, Scott G, Steffen D, Sodergren E, Wheeler DA, Worley KC, Ainscough R, Ambrose KD, Ansari-Lari MA, Aradhya S, Ashwell RI, Babbage AK, Bagguley CL, Ballabio A, Banerjee R, Barker GE, Barlow KF, Barrett IP, Bates KN, Beare DM, Beasley H, Beasley O, Beck A, Bethel G, Blechschmidt K, Brady N, Bray-Allen S, Bridgeman AM, Brown AJ, Brown MJ, Bonnin D, Bruford EA, Buhay C, Burch P, Burford D, Burgess J, Burrill W, Burton J, Bye JM, Carder C, Carrel L, Chako J, Chapman JC, Chavez D, Chen E, Chen G, Chen Y, Chen Z, Chinault C, Ciccodicola A, Clark SY, Clarke G, Clee CM, Clegg S, Clerc-Blankenburg K, Clifford K, Cobley V, Cole CG, Conquer JS, Corby N, Connor RE, David R, Davies J, Davis C, Davis J, Delgado O, Deshazo D, Dhami P, Ding Y, Dinh H, Dodsworth S, Draper H, Dugan-Rocha S, Dunham A, Dunn M, Durbin KJ, Dutta I, Eades T, Ellwood M, Emery-Cohen A, Errington H, Evans KL, Faulkner L, Francis F, Frankland J, Fraser AE, Galgoczy P, Gilbert J, Gill R, Glöckner G, Gregory SG, Gribble S, Griffiths C, Grocock R, Gu Y, Gwilliam R, Hamilton C, Hart EA, Hawes A, Heath PD, Heitmann K, Hennig S, Hernandez J, Hinzmann B, Ho S, Hoffs M, Howden PJ, Huckle EJ, Hume J, Hunt PJ, Hunt AR, Isherwood J, Jacob L, Johnson D, Jones S, de Jong PJ, Joseph SS, Keenan S, Kelly S, Kershaw JK, Khan Z, Kioschis P, Klages S, Knights AJ, Kosiura A, Kovar-Smith C, Laird GK, Langford C, Lawlor S, Leversha M, Lewis L, Liu W, Lloyd C, Lloyd DM, Loulseged H, Loveland JE, Lovell JD, Lozado R, Lu J, Lyne R, Ma J, Maheshwari M, Matthews LH, McDowall J, McLaren S, McMurray A, Meidl P, Meitinger T, Milne S, Miner G, Mistry SL, Morgan M, Morris S, Müller I, Mullikin JC, Nguyen N, Nordsiek G, Nyakatura G, O'Dell CN, Okwuonu G, Palmer S, Pandian R, Parker D, Parrish J, Pasternak S, Patel D, Pearce AV, Pearson DM, Pelan SE, Perez L, Porter KM, Ramsey Y, Reichwald K, Rhodes S, Ridler KA, Schlessinger D, Schueler MG, Sehra HK, Shaw-Smith C, Shen H, Sheridan EM, Shownkeen R, Skuce CD, Smith ML, Sotheran EC, Steingruber HE, Steward CA, Storey R, Swann RM, Swarbreck D, Tabor PE, Taudien S, Taylor T, Teague B, Thomas K, Thorpe A, Timms K, Tracey A, Trevanion S, Tromans AC, d'Urso M, Verduzco D, Villasana D, Waldron L, Wall M, Wang Q, Warren J, Warry GL, Wei X, West A, Whitehead SL, Whiteley MN, Wilkinson JE, Willey DL, Williams G, Williams L, Williamson A, Williamson H, Wilming L, Woodmansey RL, Wray PW, Yen J, Zhang J, Zhou J, Zoghbi H, Zorilla S, Buck D, Reinhardt R, Poustka A, Rosenthal A, Lehrach H, Meindl A, Minx PJ, Hillier LW, Willard HF, Wilson RK, Waterston RH, Rice CM, Vaudin M, Coulson A, Nelson DL, Weinstock G, Sulston JE, Durbin R, Hubbard T, Gibbs RA, Beck S, Rogers J, Bentley DR.

    Nature. 2005 Mar 17;434(7031):325-37.PMID: 15772651 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin.

    Otto EA, Loeys B, Khanna H, Hellemans J, Sudbrak R, Fan S, Muerb U, O'Toole JF, Helou J, Attanasio M, Utsch B, Sayer JA, Lillo C, Jimeno D, Coucke P, De Paepe A, Reinhardt R, Klages S, Tsuda M, Kawakami I, Kusakabe T, Omran H, Imm A, Tippens M, Raymond PA, Hill J, Beales P, He S, Kispert A, Margolis B, Williams DS, Swaroop A, Hildebrandt F.

    Nat Genet. 2005 Mar;37(3):282-8. Epub 2005 Feb 20.PMID: 15723066 [PubMed - indexed for MEDLINE]Related articles

    7.

    Mono-allelic expression of the IGF-I receptor does not affect IGF responses in human fibroblasts.

    Hammer E, Kutsche K, Haag F, Ullrich K, Sudbrak R, Willig RP, Braulke T, Kubler B.

    Eur J Endocrinol. 2004 Oct;151(4):521-9.PMID: 15476454 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

    Human versus chimpanzee chromosome-wide sequence comparison and its evolutionary implication.

    Sakaki Y, Watanabe H, Taylor T, Hattori M, Fujiyama A, Toyoda A, Kuroki Y, Itoh T, Saitou N, Oota S, Kim CG, Kitano T, Lehrach H, Yaspo ML, Sudbrak R, Kahla A, Reinhardt R, Kube M, Platzer M, Taenzer S, Galgoczy P, Kel A, Blöecker H, Scharfe M, Nordsiek G, Hellmann I, Khaitovich P, Pääbo S, Chen Z, Wang SY, Ren SX, Zhang XL, Zheng HJ, Zhu GF, Wang BF, Zhao GP, Tsai SF, Wu K, Liu TT, Hsiao KJ, Park HS, Lee YS, Cheong JE, Choi SH; Chimpanzee Chromosome 22 Sequencing Consortium.

    Cold Spring Harb Symp Quant Biol. 2003;68:455-60. No abstract available. PMID: 15338648 [PubMed - indexed for MEDLINE]Related articles

    9.

    DNA sequence and comparative analysis of chimpanzee chromosome 22.

    Watanabe H, Fujiyama A, Hattori M, Taylor TD, Toyoda A, Kuroki Y, Noguchi H, BenKahla A, Lehrach H, Sudbrak R, Kube M, Taenzer S, Galgoczy P, Platzer M, Scharfe M, Nordsiek G, Blöcker H, Hellmann I, Khaitovich P, Pääbo S, Reinhardt R, Zheng HJ, Zhang XL, Zhu GF, Wang BF, Fu G, Ren SX, Zhao GP, Chen Z, Lee YS, Cheong JE, Choi SH, Wu KM, Liu TT, Hsiao KJ, Tsai SF, Kim CG, OOta S, Kitano T, Kohara Y, Saitou N, Park HS, Wang SY, Yaspo ML, Sakaki Y.

    Nature. 2004 May 27;429(6990):382-8.PMID: 15164055 [PubMed - indexed for MEDLINE]Related articles

    10.

    The genomic sequence and comparative analysis of the rat major histocompatibility complex.

    Hurt P, Walter L, Sudbrak R, Klages S, Müller I, Shiina T, Inoko H, Lehrach H, Günther E, Reinhardt R, Himmelbauer H.

    Genome Res. 2004 Apr;14(4):631-9.PMID: 15060004 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    Plasticity of human chromosome 3 during primate evolution.

    Tsend-Ayush E, Grützner F, Yue Y, Grossmann B, Hänsel U, Sudbrak R, Haaf T.

    Genomics. 2004 Feb;83(2):193-202.PMID: 14706448 [PubMed - indexed for MEDLINE]Related articles

    12.

    Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis.

    Olbrich H, Fliegauf M, Hoefele J, Kispert A, Otto E, Volz A, Wolf MT, Sasmaz G, Trauer U, Reinhardt R, Sudbrak R, Antignac C, Gretz N, Walz G, Schermer B, Benzing T, Hildebrandt F, Omran H.

    Nat Genet. 2003 Aug;34(4):455-9.PMID: 12872122 [PubMed - indexed for MEDLINE]Related articles

    13.

    Comparative and evolutionary analysis of the rhesus macaque extended MHC class II region.

    Sudbrak R, Reinhardt R, Hennig S, Lehrach H, Günther E, Walter L.

    Immunogenetics. 2003 Jan;54(10):699-704. Epub 2002 Dec 10.PMID: 12557056 [PubMed - indexed for MEDLINE]Related articles

    14.

    A gene mutated in nephronophthisis and retinitis pigmentosa encodes a novel protein, nephroretinin, conserved in evolution.

    Otto E, Hoefele J, Ruf R, Mueller AM, Hiller KS, Wolf MT, Schuermann MJ, Becker A, Birkenhäger R, Sudbrak R, Hennies HC, Nürnberg P, Hildebrandt F.

    Am J Hum Genet. 2002 Nov;71(5):1161-7. Epub 2002 Aug 29.PMID: 12205563 [PubMed - indexed for MEDLINE]Related articlesFree article

    15.

    Physical mapping of the major histocompatibility complex class II and class III regions of the rat.

    Walter L, Hurt P, Himmelbauer H, Sudbrak R, Günther E.

    Immunogenetics. 2002 Jul;54(4):268-75. Epub 2002 Jun 14.PMID: 12136338 [PubMed - indexed for MEDLINE]Related articles

    16.

    Gene for integrin-associated protein (IAP, CD47): physical mapping, genomic structure, and expression studies in skeletal muscle.

    Schickel J, Stahn K, Zimmer KP, Sudbrak R, Størm TM, Dürst M, Kiehntopf M, Deufel T.

    Biochem Cell Biol. 2002;80(2):169-76.PMID: 11989712 [PubMed - indexed for MEDLINE]Related articles

    17.

    Hailey-Hailey disease: molecular and clinical characterization of novel mutations in the ATP2C1 gene.

    Dobson-Stone C, Fairclough R, Dunne E, Brown J, Dissanayake M, Munro CS, Strachan T, Burge S, Sudbrak R, Monaco AP, Hovnanian A.

    J Invest Dermatol. 2002 Feb;118(2):338-43.PMID: 11841554 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry.

    Olbrich H, Häffner K, Kispert A, Völkel A, Volz A, Sasmaz G, Reinhardt R, Hennig S, Lehrach H, Konietzko N, Zariwala M, Noone PG, Knowles M, Mitchison HM, Meeks M, Chung EM, Hildebrandt F, Sudbrak R, Omran H.

    Nat Genet. 2002 Feb;30(2):143-4. Epub 2002 Jan 14.PMID: 11788826 [PubMed - indexed for MEDLINE]Related articles

    19.

    ACRC codes for a novel nuclear protein with unusual acidic repeat tract and maps to DYT3 (dystonia parkinsonism) critical interval in xq13.1.

    Nolte D, Ramser J, Niemann S, Lehrach H, Sudbrak R, Müller U.

    Neurogenetics. 2001 Oct;3(4):207-13.PMID: 11714101 [PubMed - indexed for MEDLINE]Related articles

    20.

    Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure.

    Birkenhäger R, Otto E, Schürmann MJ, Vollmer M, Ruf EM, Maier-Lutz I, Beekmann F, Fekete A, Omran H, Feldmann D, Milford DV, Jeck N, Konrad M, Landau D, Knoers NV, Antignac C, Sudbrak R, Kispert A, Hildebrandt F.

    Nat Genet. 2001 Nov;29(3):310-4.PMID: 11687798 [PubMed - indexed for MEDLINE]Related articles

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