Works in Nature Genetics, 2003, Vol 34, Issue 4

Results: 27
    1

    Krogh's principle for a new era.

    Published in:
    2003
    By:
    • Vaingankar, Sucheta;
    • Toliat, Mohammad R.;
    • Suk, Anita;
    • Höhne, Wolfgang;
    • Schauer, Galen;
    • Lehmann, Mandy;
    • Roscioli, Tony;
    • Schnabel, Dirk;
    • Epplen, Jörg T.;
    • Knisley, Alex;
    • Superti-Furga, Andrea;
    • McGill, James;
    • Filippone, Marco;
    • Sinaiko, Alan R.;
    • Vallance, Hillary;
    • Hinrichs, Bernd;
    • Smith, Wendy
    Publication type:
    Editorial
    2
    3
    4
    5

    From cilia to cyst.

    Published in:
    Nature Genetics, 2003, v. 34, n. 4, p. 355, doi. 10.1038/ng0803-355
    By:
    • Watnick, Terry;
    • Germino, Gregory
    Publication type:
    Article
    6

    A new piece of the ALS puzzle.

    Published in:
    Nature Genetics, 2003, v. 34, n. 4, p. 357, doi. 10.1038/ng0803-357
    By:
    • Cleveland, John L.
    Publication type:
    Article
    7

    Peeking under QTL peaks.

    Published in:
    Nature Genetics, 2003, v. 34, n. 4, p. 358, doi. 10.1038/ng0803-358
    By:
    • Curtsinger, James W.
    Publication type:
    Article
    8

    Ensuring enhancer fidelity.

    Published in:
    Nature Genetics, 2003, v. 34, n. 4, p. 360, doi. 10.1038/ng0803-360
    By:
    • Maeda, Robert K.;
    • Karch, François
    Publication type:
    Article
    9

    Touchingbase.

    Published in:
    Nature Genetics, 2003, v. 34, n. 4, p. 363, doi. 10.1038/ng0803-363
    By:
    • Gresham, David;
    • Packer, Alan;
    • Stebbins, Michael
    Publication type:
    Article
    10

    Research Notes.

    Published in:
    Nature Genetics, 2003, v. 34, n. 4, p. 364, doi. 10.1038/ng0803-364
    By:
    • Gresham, David;
    • Packer, Alan;
    • Stebbins, Michael
    Publication type:
    Article
    11
    12
    13

    Functional haplotypes of PADI4, encoding citrullinating enzyme peptidylarginine deiminase 4, are associated with rheumatoid arthritis.

    Published in:
    Nature Genetics, 2003, v. 34, n. 4, p. 395, doi. 10.1038/ng1206
    By:
    • Suzuki, Akari;
    • Yamada, Ryo;
    • Chang, Xiaotian;
    • Tokuhiro, Shinya;
    • Sawada, Tetsuji;
    • Suzuki, Masakatsu;
    • Nagasaki, Miyuki;
    • Nakayama-Hamada, Makiko;
    • Kawaida, Reimi;
    • Ono, Mitsuru;
    • Ohtsuki, Masahiko;
    • Furukawa, Hidehiko;
    • Yoshino, Shinichi;
    • Yukioka, Masao;
    • Tohma, Shigeto;
    • Matsubara, Tsukasa;
    • Wakitani, Shigeyuki;
    • Teshima, Ryota;
    • Nishioka, Yuichi
    Publication type:
    Article
    14
    15

    Mutations in the genes encoding 11ß-hydroxysteroid dehydrogenase type 1 and hexose-6-phosphate dehydrogenase interact to cause cortisone reductase deficiency.

    Published in:
    Nature Genetics, 2003, v. 34, n. 4, p. 434, doi. 10.1038/ng1214
    By:
    • Draper, Nicole;
    • Walker, Elizabeth A.;
    • Bujalska, Iwona J.;
    • Tomlinson, Jeremy W.;
    • Chalder, Susan M.;
    • Arlt, Wiebke;
    • Lavery, Gareth G.;
    • Bedendo, Oliver;
    • Ray, David W.;
    • Laing, Ian;
    • Malunowicz, Ewa;
    • White, Perrin C.;
    • Hewison, Martin;
    • Mason, Philip J.;
    • Connell, John M.;
    • Shackleton, Cedric H.L.;
    • Stewart, Paul M.
    Publication type:
    Article
    16

    Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31.

    Published in:
    Nature Genetics, 2003, v. 34, n. 4, p. 421, doi. 10.1038/ng1208
    By:
    • Mburu, Philomena;
    • Mustapha, Mirna;
    • Varela, Anabel;
    • Weil, Dominique;
    • El-Amraoui, Aziz;
    • Holme, Ralph H.;
    • Rump, Andreas;
    • Hardisty, Rachel E.;
    • Blanchard, Stéphane;
    • Coimbra, Roney S.;
    • Perfettini, Isabele;
    • Parkinson, Nick;
    • Mallon, Ann-Marie;
    • Glenister, Pete;
    • Rogers, Mike J.;
    • Paige, Adam J.;
    • Moir, Lee;
    • Clay, Jo;
    • Rosenthal, Andre
    Publication type:
    Article
    17

    Chromosome aberrations in solid tumors.

    Published in:
    Nature Genetics, 2003, v. 34, n. 4, p. 369, doi. 10.1038/ng1215
    By:
    • Albertson, Donna G.;
    • Collins, Colin;
    • McCormick, Frank;
    • Gray, Joe W.
    Publication type:
    Article
    18

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

    Published in:
    Nature Genetics, 2003, v. 34, n. 4, p. 455, doi. 10.1038/ng1216
    By:
    • Olbrich, Heike;
    • Fliegauf, Manfred;
    • Hoefele, Julia;
    • Kispert, Andreas;
    • Otto, Edgar;
    • Volz, Andreas;
    • Wolf, Matthias T.;
    • Sasmaz, Gürsel;
    • Trauer, Ute;
    • Reinhardt, Richard;
    • Sudbrak, Ralf;
    • Antignac, Corinne;
    • Gretz, Norbert;
    • Walz, Gerd;
    • Schermer, Bernhard;
    • Benzing, Thomas;
    • Hildebrandt, Friedhelm;
    • Omran, Heymut
    Publication type:
    Article
    19
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    22

    VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death.

    Published in:
    Nature Genetics, 2003, v. 34, n. 4, p. 383, doi. 10.1038/ng1211
    By:
    • Lambrechts, Diether;
    • Storkebaum, Erik;
    • Morimoto, Masafumi;
    • Del-Favero, Jurgen;
    • Desmet, Frederik;
    • Marklund, Stefan L.;
    • Wyns, Sabine;
    • Thijs, Vincent;
    • Andersson, Jörgen;
    • van Marion, Ingrid;
    • Al-Chalabi, Ammar;
    • Bornes, Stephanie;
    • Musson, Rhiannon;
    • Hansen, Valerie;
    • Beckman, Lars;
    • Adolfsson, Rolf;
    • Pall, Hardev Singh;
    • Prats, Hervé;
    • Vermeire, Severine
    Publication type:
    Article
    23
    24

    Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination.

    Published in:
    Nature Genetics, 2003, v. 34, n. 4, p. 413, doi. 10.1038/ng1217
    By:
    • Otto, Edgar A.;
    • Schermer, Bernhard;
    • Obara, Tomoko;
    • O'Toole, John F.;
    • Hiller, Karl S.;
    • Mueller, Adelheid M.;
    • Ruf, Rainer G.;
    • Hoefele, Julia;
    • Beekmann, Frank;
    • Landau, Daniel;
    • Foreman, John W.;
    • Goodship, Judith A.;
    • Strachan, Tom;
    • Kispert, Andreas;
    • Wolf, Matthias T.;
    • Gagnadoux, Marie F.;
    • Nivet, Hubert;
    • Antignac, Corine;
    • Walz, Gerd
    Publication type:
    Article
    25
    26
    27

    Mutations in ENPP1 are associated with 'idiopathic' infantile arterial calcification.

    Published in:
    Nature Genetics, 2003, v. 34, n. 4, p. 379, doi. 10.1038/ng1221
    By:
    • Rutsch, Frank;
    • Ruf, Nico;
    • Vaingankar, Sucheta;
    • Toliat, Mohammed R.;
    • Suk, Anita;
    • Höhne, Wolfgang;
    • Schauer, Galen;
    • Lehmann, Mandy;
    • Roscioli, Tony;
    • Schnabel, Dirk;
    • Epplen, Jörg T.;
    • Knisely, Alex;
    • Superti-Furga, Andrea;
    • McGill, James;
    • Filippone, Marco;
    • Sinaiko, Alan R.;
    • Vallance, Hillary;
    • Hinrichs, Bernd;
    • Smith, Wendy
    Publication type:
    Article