Works by Kaur, Maninder

Results: 261
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    Transcriptional Dysregulation in NIPBL and Cohesin Mutant Human Cells.

    Published in:
    PLoS Biology, 2009, v. 7, n. 5, p. 1, doi. 10.1371/journal.pbio.1000119
    By:
    • Jinglan Liu;
    • Zhe Zhang;
    • Bando, Masashige;
    • Itoh, Takehiko;
    • Deardorff, Matthew A.;
    • Clark, Dinah;
    • Kaur, Maninder;
    • Tandy, Stephany;
    • Kondoh, Tatsuro;
    • Rappaport, Eric;
    • Spinner, Nancy B.;
    • Vega, Hugo;
    • Jackson, Laird G.;
    • Shirahige, Katsuhiko;
    • Krantz, Ian D.
    Publication type:
    Article
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    Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype–phenotype correlations and common mechanisms.

    Published in:
    American Journal of Medical Genetics. Part A, 2023, v. 191, n. 8, p. 2113, doi. 10.1002/ajmg.a.63247
    By:
    • Kaur, Maninder;
    • Blair, Justin;
    • Devkota, Batsal;
    • Fortunato, Sierra;
    • Clark, Dinah;
    • Lawrence, Audrey;
    • Kim, Jiwoo;
    • Do, Wonwook;
    • Semeo, Benjamin;
    • Katz, Olivia;
    • Mehta, Devanshi;
    • Yamamoto, Nobuko;
    • Schindler, Emma;
    • Al Rawi, Zayd;
    • Wallace, Nina;
    • Wilde, Jonathan J.;
    • McCallum, Jennifer;
    • Liu, Jinglan;
    • Xu, Dongbin;
    • Jackson, Marie
    Publication type:
    Article
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    Genome-wide DNA methylation analysis in cohesin mutant human cell lines.

    Published in:
    Nucleic Acids Research, 2010, v. 38, n. 17, p. 5657, doi. 10.1093/nar/gkq346
    By:
    • Liu, Jinglan;
    • Zhang, Zhe;
    • Bando, Masashige;
    • Itoh, Takehiko;
    • Deardorff, Matthew A.;
    • Li, Jennifer R.;
    • Clark, Dinah;
    • Kaur, Maninder;
    • Tatsuro, Kondo;
    • Kline, Antonie D.;
    • Chang, Celia;
    • Vega, Hugo;
    • Jackson, Laird G.;
    • Spinner, Nancy B.;
    • Shirahige, Katsuhiko;
    • Krantz, Ian D.
    Publication type:
    Article
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    Isolated NIPBL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction.

    Published in:
    2012
    By:
    • Braunholz, Diana;
    • Hullings, Melanie;
    • Gil-Rodríguez, María Concepcion;
    • Fincher, Christopher T;
    • Mallozzi, Mark B;
    • Loy, Elizabeth;
    • Albrecht, Melanie;
    • Kaur, Maninder;
    • Limon, Janusz;
    • Rampuria, Abhinav;
    • Clark, Dinah;
    • Kline, Antonie;
    • Dalski, Andreas;
    • Eckhold, Juliane;
    • Tzschach, Andreas;
    • Hennekam, Raoul;
    • Gillessen-Kaesbach, Gabriele;
    • Wierzba, Jolanta;
    • Krantz, Ian D;
    • Deardorff, Matthew A
    Publication type:
    Correction Notice
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    Isolated NIBPL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction.

    Published in:
    European Journal of Human Genetics, 2012, v. 20, n. 3, p. 271, doi. 10.1038/ejhg.2011.175
    By:
    • Braunholz, Diana;
    • Hullings, Melanie;
    • Gil-Rodríguez, María Concepcion;
    • Fincher, Christopher T;
    • Mallozzi, Mark B;
    • Loy, Elizabeth;
    • Albrecht, Melanie;
    • Kaur, Maninder;
    • Limon, Janusz;
    • Rampuria, Abhinav;
    • Clark, Dinah;
    • Kline, Antonie;
    • Dalski, Andreas;
    • Eckhold, Juliane;
    • Tzschach, Andreas;
    • Hennekam, Raoul;
    • Gillessen-Kaesbach, Gabriele;
    • Wierzba, Jolanta;
    • Krantz, Ian D;
    • Deardorff, Matthew A
    Publication type:
    Article
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    Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B.

    Published in:
    Nature Genetics, 2004, v. 36, n. 6, p. 631, doi. 10.1038/ng1364
    By:
    • Krantz, Ian D.;
    • McCallum, Jennifer;
    • DeScipio, Cheryl;
    • Kaur, Maninder;
    • Gillis, Lynette A.;
    • Yaeger, Dinah;
    • Jukofsky, Lori;
    • Wasserman, Nora;
    • Bottani, Armand;
    • Morris, Colleen A.;
    • Nowaczyk, Malgorzata J. M.;
    • Toriello, Helga;
    • Bamshad, Michael J.;
    • Carey, John C.;
    • Rappaport, Eric;
    • Kawauchi, Shimako;
    • Lander, Arthur D.;
    • Calof, Anne L.;
    • Hui-Hua Li;
    • Devoto, Marcella
    Publication type:
    Article
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