Works matching AU Kanapin, Alexander


Results: 33
    1

    The Genetic Landscape of Fiber Flax.

    Published in:
    Frontiers in Plant Science, 2021, v. 12, p. 1, doi. 10.3389/fpls.2021.764612
    By:
    • Duk, Maria;
    • Kanapin, Alexander;
    • Rozhmina, Tatyana;
    • Bankin, Mikhail;
    • Surkova, Svetlana;
    • Samsonova, Anastasia;
    • Samsonova, Maria
    Publication type:
    Article
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    Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis.

    Published in:
    Nature Genetics, 2013, v. 45, n. 10, p. 1261, doi. 10.1038/ng1013-1261a
    By:
    • Sharma, Vikram P;
    • Fenwick, Aimée L;
    • Brockop, Mia S;
    • McGowan, Simon J;
    • Goos, Jacqueline A C;
    • Hoogeboom, A Jeannette M;
    • Brady, Angela F;
    • Jeelani, Nu Owase;
    • Lynch, Sally Ann;
    • Mulliken, John B;
    • Murray, Dylan J;
    • Phipps, Julie M;
    • Sweeney, Elizabeth;
    • Tomkins, Susan E;
    • Wilson, Louise C;
    • Bennett, Sophia;
    • Cornall, Richard J;
    • Broxholme, John;
    • Kanapin, Alexander;
    • Johnson, David
    Publication type:
    Article
    6

    Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis.

    Published in:
    Nature Genetics, 2013, v. 45, n. 3, p. 304, doi. 10.1038/ng.2531
    By:
    • Sharma, Vikram P;
    • Fenwick, Aimée L;
    • Brockop, Mia S;
    • McGowan, Simon J;
    • Goos, Jacqueline A C;
    • Hoogeboom, A Jeannette M;
    • Brady, Angela F;
    • Jeelani, Nu Owase;
    • Lynch, Sally Ann;
    • Mulliken, John B;
    • Murray, Dylan J;
    • Phipps, Julie M;
    • Sweeney, Elizabeth;
    • Tomkins, Susan E;
    • Wilson, Louise C;
    • Bennett, Sophia;
    • Cornall, Richard J;
    • Broxholme, John;
    • Kanapin, Alexander;
    • Johnson, David
    Publication type:
    Article
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    A point mutation in the ion conduction pore of AMP A receptor GRIA3 causes dramatically perturbed sleep patterns as well as intellectual disability.

    Published in:
    Human Molecular Genetics, 2017, v. 26, n. 20, p. 3869, doi. 10.1093/hmg/ddx270
    By:
    • Davies, Benjamin;
    • Brown, Laurence A.;
    • Cais, Ondrej;
    • Watson, Jake;
    • Clayton, Amber J.;
    • Chang, Veronica T.;
    • Biggs, Daniel;
    • Preece, Christopher;
    • Hernandez-Pliego, Polinka;
    • Krohn, Jon;
    • Bhomra, Amarjit;
    • Twigg, Stephen R. F.;
    • Rimmer, Andrew;
    • Kanapin, Alexander;
    • Sen, Arjune;
    • Zaiwalla, Zenobia;
    • McVean, Gil;
    • Foster, Russell;
    • Donnelly, Peter;
    • Taylor, Jenny C.
    Publication type:
    Article
    10

    Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis.

    Published in:
    Human Molecular Genetics, 2014, v. 23, n. 12, p. 3200
    By:
    • Martin, Hilary C.;
    • Kim, Grace E.;
    • Pagnamenta, Alistair T.;
    • Murakami, Yoshiko;
    • Carvill, Gemma L.;
    • Meyer, Esther;
    • Copley, Richard R.;
    • Rimmer, Andrew;
    • Barcia, Giulia;
    • Fleming, Matthew R.;
    • Kronengold, Jack;
    • Brown, Maile R.;
    • Hudspith, Karl A.;
    • Broxholme, John;
    • Kanapin, Alexander;
    • Cazier, Jean-Baptiste;
    • Kinoshita, Taroh;
    • Nabbout, Rima;
    • Bentley, David;
    • McVean, Gil
    Publication type:
    Article
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    RASSF1A uncouples Wnt from Hippo signalling and promotes YAP mediated differentiation via p73.

    Published in:
    Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-017-02786-5
    By:
    • Papaspyropoulos, Angelos;
    • Bradley, Leanne;
    • Thapa, Asmita;
    • Chuen Yan Leung;
    • Toskas, Konstantinos;
    • Koennig, Delia;
    • Pefani, Dafni-Eleftheria;
    • Raso, Cinzia;
    • Grou, Claudia;
    • Hamilton, Garth;
    • Vlahov, Nikola;
    • Grawenda, Anna;
    • Haider, Syed;
    • Chauhan, Jagat;
    • Buti, Ludovico;
    • Kanapin, Alexander;
    • Xin Lu;
    • Buffa, Francesca;
    • Dianov, Grigory;
    • von Kriegsheim, Alex
    Publication type:
    Article
    13

    Applications of InterPro in protein annotation and genome analysis.

    Published in:
    Briefings in Bioinformatics, 2002, v. 3, n. 3, p. 285, doi. 10.1093/bib/3.3.285
    By:
    • Biswas, Margaret;
    • O'Rourke, John F.;
    • Camon, Evelyn;
    • Fraser, Gill;
    • Kanapin, Alexander;
    • Karavidopoulou, Youla;
    • Kersey, Paul;
    • Kriventseva, Evgenia;
    • Mittard, Virginie;
    • Mulder, Nicola;
    • Phan, Isabelle;
    • Servant, Florence;
    • Apweiler, Rolf
    Publication type:
    Article
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    A Genome-Wide Association Study Reveals a BDNF -Centered Molecular Network Associated with Alcohol Dependence and Related Clinical Measures.

    Published in:
    Biomedicines, 2022, v. 10, n. 12, p. 3007, doi. 10.3390/biomedicines10123007
    By:
    • Levchenko, Anastasia;
    • Malov, Sergey;
    • Antonik, Alexey;
    • Protsvetkina, Anastasia;
    • Rybakova, Kseniya V.;
    • Kanapin, Alexander;
    • Yakovlev, Alexey N.;
    • Nenasteva, Anna Y.;
    • Nikolishin, Anton E.;
    • Cherkasov, Nikolay;
    • Chuprova, Natalia A.;
    • Blagonravova, Anna S.;
    • Sergeeva, Angelica V.;
    • Zhilyaeva, Tatyana V.;
    • Denisenko, Maria K.;
    • Gainetdinov, Raul R.;
    • Kibitov, Alexander O.;
    • Krupitsky, Evgeny M.
    Publication type:
    Article
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    Integr8 and Genome Reviews: integrated views of complete genomes and proteomes.

    Published in:
    Nucleic Acids Research, 2005, v. 33, n. suppl 1, p. d297
    By:
    • Kersey, Paul;
    • Bower, Lawrence;
    • Morris, Lorna;
    • Horne, Alan;
    • Petryszak, Robert;
    • Kanz, Carola;
    • Kanapin, Alexander;
    • Das, Ujjwal;
    • Michoud, Karine;
    • Phan, Isabelle;
    • Gattiker, Alexandre;
    • Kulikova, Tamara;
    • Faruque, Nadeem;
    • Duggan, Karyn;
    • Mclaren, Peter;
    • Reimholz, Britt;
    • Duret, Laurent;
    • Penel, Simon;
    • Reuter, Ingmar;
    • Apweiler, Rolf
    Publication type:
    Article
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    Recessive Mutations in SPTBN2 Implicate β-III Spectrin in Both Cognitive and Motor Development.

    Published in:
    PLoS Genetics, 2012, v. 8, n. 12, p. 1, doi. 10.1371/journal.pgen.1003074
    By:
    • Lise, Stefano;
    • Clarkson, Yvonne;
    • Perkins, Emma;
    • Kwasniewska, Alexandra;
    • Akha, Elham Sadighi;
    • Schnekenberg, Ricardo Parolin;
    • Suminaite, Daumante;
    • Hope, Jilly;
    • Baker, Ian;
    • Gregory, Lorna;
    • Green, Angie;
    • Allan, Chris;
    • Lamble, Sarah;
    • Jayawant, Sandeep;
    • Quaghebeur, Gerardine;
    • Cader, M. Zameel;
    • Hughes, Sarah;
    • Armstrong, Richard J. E.;
    • Kanapin, Alexander;
    • Rimmer, Andrew
    Publication type:
    Article