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CRM Publications

Found 59 results
Filters: Keyword is Mutation  [Clear All Filters]
2009
Ho H-Y, Chang K-H, Nichols J, Li M.  2009.  Homeodomain protein Pitx3 maintains the mitotic activity of lens epithelial cells.Mech Dev. 126(1-2):18-29.
2006
Foukas LC, Claret M, Pearce W, Okkenhaug K, Meek S, Peskett E, Sancho S, Smith AG, Withers DJ, Vanhaesebroeck B.  2006.  Critical role for the p110alpha phosphoinositide-3-OH kinase in growth and metabolic regulation.Nature. 441(7091):366-70.
Pollard SM, Parsons MJ, Kamei M, Kettleborough RNW, Thomas KA, Pham VN, Bae M-K, Scott A, Weinstein BM, Stemple DL.  2006.  Essential and overlapping roles for laminin alpha chains in notochord and blood vessel formation.Dev Biol. 289(1):64-76.
Morris L, Gordon J, C Blackburn C.  2006.  Identification of a tandem duplicated array in the Rhox alpha locus on mouse chromosome X.Mamm Genome. 17(2):178-87.
Bashamboo A, A Taylor H, Samuel K, Panthier J-J, Whetton AD, Forrester LM.  2006.  The survival of differentiating embryonic stem cells is dependent on the SCF-KIT pathway.J Cell Sci. 119(Pt 15):3039-46.
2005
Ohinata Y, Payer B, O'Carroll D, Ancelin K, Ono Y, Sano M, Barton SC, Obukhanych T, Nussenzweig M, Tarakhovsky A et al..  2005.  Blimp1 is a critical determinant of the germ cell lineage in mice.Nature. 436(7048):207-13.
Doumont G, Martoriati A, Beekman C, Bogaerts S, Mee PJ, Bureau F, Colombo E, Alcalay M, Bellefroid E, Marchesi F et al..  2005.  G1 checkpoint failure and increased tumor susceptibility in mice lacking the novel p53 target Ptprv.EMBO J. 24(17):3093-103.
Caballero IMartín, Hendrich B.  2005.  MeCP2 in neurons: closing in on the causes of Rett syndrome.Hum Mol Genet. 14 Spec No 1:R19-26.
Kelly K, Hutchinson G, Nebenuis-Oosthuizen D, Smith AG, Bartsch JW, Horiuchi K, Rittger A, Manova K, Docherty AJP, Blobel CP.  2005.  Metalloprotease-disintegrin ADAM8: expression analysis and targeted deletion in mice.Dev Dyn. 232(1):221-31.
2004
Garrick D, Samara V, McDowell TL, Smith AG, Dobbie L, Higgs DR, Gibbons RJ.  2004.  A conserved truncated isoform of the ATR-X syndrome protein lacking the SWI/SNF-homology domain.Gene. 326:23-34.
Tse E, Smith AG, Hunt S, Lavenir I, Forster A, Warren AJ, Grutz G, Foroni L, Carlton MBL, Colledge WH et al..  2004.  Null mutation of the Lmo4 gene or a combined null mutation of the Lmo1/Lmo3 genes causes perinatal lethality, and Lmo4 controls neural tube development in mice.Mol Cell Biol. 24(5):2063-73.
2003
Carvalho LR, Woods KS, Mendonca BB, Marcal N, Zamparini AL, Stifani S, Brickman JM, Arnhold IJP, Dattani MT.  2003.  A homozygous mutation in HESX1 is associated with evolving hypopituitarism due to impaired repressor-corepressor interaction.J Clin Invest. 112(8):1192-201.
Meunier D, Aubin J, Jeannotte L.  2003.  Perturbed thyroid morphology and transient hypothyroidism symptoms in Hoxa5 mutant mice.Dev Dyn. 227(3):367-78.
2002
Rambukkana A, Zanazzi G, Tapinos N, Salzer JL.  2002.  Contact-dependent demyelination by Mycobacterium leprae in the absence of immune cells.Science. 296(5569):927-31.
Niwa H, Masui S, Chambers I, Smith AG, Miyazaki J-ichi.  2002.  Phenotypic complementation establishes requirements for specific POU domain and generic transactivation function of Oct-3/4 in embryonic stem cells.Mol Cell Biol. 22(5):1526-36.
Brickman JM, Burdon T.  2002.  Pluripotency and tumorigenicity.Nat Genet. 32(4):557-8.
Parsons MJ, Pollard SM, Saúde L, Feldman B, Coutinho P, Hirst EMA, Stemple DL.  2002.  Zebrafish mutants identify an essential role for laminins in notochord formation.Development. 129(13):3137-46.
2001
Craig NJ, Alonso MBDurán, Hawker KL, Shiels P, Glencorse TA, Campbell JM, Bennett NK, Canham MA, Donald D, Gardiner M et al..  2001.  A candidate gene for human neurodegenerative disorders: a rat PKC gamma mutation causes a Parkinsonian syndrome.Nat Neurosci. 4(11):1061-2.
Lowell S, Watt FM.  2001.  Delta regulates keratinocyte spreading and motility independently of differentiation.Mech Dev. 107(1-2):133-40.
Lachner M, O'Carroll D, Rea S, Mechtler K, Jenuwein T.  2001.  Methylation of histone H3 lysine 9 creates a binding site for HP1 proteins.Nature. 410(6824):116-20.
Brickman JM, Clements M, Tyrell R, McNay D, Woods K, Warner J, Stewart A, Beddington RS, Dattani MT.  2001.  Molecular effects of novel mutations in Hesx1/HESX1 associated with human pituitary disorders.Development. 128(24):5189-99.
Loh NY, Nebenuis-Oosthuizen D, Blake DJ, Smith AG, Davies KE.  2001.  Role of beta-dystrobrevin in nonmuscle dystrophin-associated protein complex-like complexes in kidney and liver.Mol Cell Biol. 21(21):7442-8.
1999
Burdon T, Stracey C, Chambers I, Nichols J, Smith A.  1999.  Suppression of SHP-2 and ERK signalling promotes self-renewal of mouse embryonic stem cells.Dev Biol. 210(1):30-43.
1998
Gubenko IS, Rybtsova N, Zelentsova ES, Lezin GT, Korochkin LI, Evgen'ev MB.  1998.  [The Delta locus in Drosophila virilis: cloning and chromosome mapping].Dokl Akad Nauk. 358(4):567-9.
Migaud M, Charlesworth P, Dempster M, Webster LC, Watabe AM, Makhinson M, He Y, Ramsay MF, Morris RG, Morrison JH et al..  1998.  Enhanced long-term potentiation and impaired learning in mice with mutant postsynaptic density-95 protein.Nature. 396(6710):433-9.

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