1 - 25 of 51 results for author:"Bateman J.F." in Literature citations
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| Recurrent dominant mutations affecting two adjacent residues in the motor domain of the monomeric kinesin KIF22 result in skeletal dysplasia and joint laxity. Boyden E.D., Campos-Xavier A.B., Kalamajski S., Cameron T.L., Suarez P., Tanackovic G., Andria G., Ballhausen D., Briggs M.D., Hartley C. et al. Am. J. Hum. Genet. 89:767-772(2011) · UniProtKB (1) · Mapped (7) |
| Mutations in TRPV4 cause an inherited arthropathy of hands and feet. Lamande S.R., Yuan Y., Gresshoff I.L., Rowley L., Belluoccio D., Kaluarachchi K., Little C.B., Botzenhart E., Zerres K., Amor D.J. et al. Nat. Genet. 43:1142-1146(2011) · UniProtKB (1) |
| Transcriptional profiling of chondrodysplasia growth plate cartilage reveals adaptive ER-stress networks that allow survival but disrupt hypertrophy. Cameron T.L., Bell K.M., Tatarczuch L., Mackie E.J., Rajpar M.H., McDermott B.T., Boot-Handford R.P., Bateman J.F. PLoS ONE 6:e24600-e24600(2011) · Mapped (1) |
| Cartilage intermediate layer protein 2 (CILP-2) is expressed in articular and meniscal cartilage and down-regulated in experimental osteoarthritis. Bernardo B.C., Belluoccio D., Rowley L., Little C.B., Hansen U., Bateman J.F. J. Biol. Chem. 286:37758-37767(2011) · Mapped (7) |
| Collagen VI microfibril formation is abolished by an {alpha}2(VI) von Willebrand factor type A domain mutation in a patient with Ullrich congenital muscular dystrophy. Tooley L.D., Zamurs L.K., Beecher N., Baker N.L., Peat R.A., Adams N.E., Bateman J.F., North K.N., Baldock C., Lamande S.R. J. Biol. Chem. 285:33567-33576(2010) · Mapped (6) |
| Sorting of growth plate chondrocytes allows the isolation and characterization of cells of a defined differentiation status. Belluoccio D., Etich J., Rosenbaum S., Frie C., Grskovic I., Stermann J., Ehlen H., Vogel S., Zaucke F., von der Mark K. et al. J. Bone Miner. Res. 25:1267-1281(2010) · Mapped (54) |
| Premature arthritis is a distinct type II collagen phenotype. Kannu P., Bateman J.F., Randle S., Cowie S., du Sart D., McGrath S., Edwards M., Savarirayan R. Arthritis Rheum. 62:1421-1430(2010) · Mapped (4) |
| S100A8 and S100A9 in experimental osteoarthritis. Zreiqat H., Belluoccio D., Smith M.M., Wilson R., Rowley L.A., Jones K., Ramaswamy Y., Vogl T., Roth J., Bateman J.F. et al. Arthritis Res. Ther. 12:R16-R16(2010) · Mapped (2) |
| Targeted induction of endoplasmic reticulum stress induces cartilage pathology. Rajpar M.H., McDermott B., Kung L., Eardley R., Knowles L., Heeran M., Thornton D.J., Wilson R., Bateman J.F., Poulsom R. et al. PLoS Genet. 5:e1000691-e1000691(2009) · Mapped (1) |
| Deficiency of annexins A5 and A6 induces complex changes in the transcriptome of growth plate cartilage but does not inhibit the induction of mineralization. Belluoccio D., Grskovic I., Niehoff A., Schlotzer-Schrehardt U., Rosenbaum S., Etich J., Frie C., Pausch F., Moss S.E., Poschl E. et al. J. Bone Miner. Res. 25:141-153(2010) · Mapped (10) |
| Mice lacking the extracellular matrix protein WARP develop normally but have compromised peripheral nerve structure and function. Allen J.M., Zamurs L., Brachvogel B., Schlotzer-Schrehardt U., Hansen U., Lamande S.R., Rowley L., Fitzgerald J., Bateman J.F. J. Biol. Chem. 284:12020-12030(2009) · Mapped (1) |
| Global comparative transcriptome analysis of cartilage formation in vivo. Cameron T.L., Belluoccio D., Farlie P.G., Brachvogel B., Bateman J.F. BMC Dev. Biol. 9:20-20(2009) · Mapped (40) |
| Collagen VI glycine mutations: perturbed assembly and a spectrum of clinical severity. Pace R.A., Peat R.A., Baker N.L., Zamurs L., Morgelin M., Irving M., Adams N.E., Bateman J.F., Mowat D., Smith N.J. et al. Ann. Neurol. 64:294-303(2008) · Mapped (6) |
| The extracellular matrix protein WARP is a novel component of a distinct subset of basement membranes. Allen J.M., Brachvogel B., Farlie P.G., Fitzgerald J., Bateman J.F. |
| Competency for nonsense-mediated reduction in collagen X mRNA is specified by the 3' UTR and corresponds to the position of mutations in Schmid metaphyseal chondrodysplasia. Tan J.T., Kremer F., Freddi S., Bell K.M., Baker N.L., Lamande S.R., Bateman J.F. Am. J. Hum. Genet. 82:786-793(2008) · Mapped (1) |
| Molecular consequences of dominant Bethlem myopathy collagen VI mutations. Baker N.L., Moergelin M., Pace R.A., Peat R.A., Adams N.E., Gardner R.J., Rowland L.P., Miller G., De Jonghe P., Ceulemans B. et al. Ann. Neurol. 62:390-405(2007) · UniProtKB (2) |
| Isolated Anxa5+/Sca-1+ perivascular cells from mouse meningeal vasculature retain their perivascular phenotype in vitro and in vivo. Brachvogel B., Pausch F., Farlie P., Gaipl U., Etich J., Zhou Z., Cameron T., von der Mark K., Bateman J.F., Poschl E. Exp. Cell Res. 313:2730-2743(2007) · Mapped (4) |
| WARP is a novel multimeric component of the chondrocyte pericellular matrix that interacts with perlecan. Allen J.M., Bateman J.F., Hansen U., Wilson R., Bruckner P., Owens R.T., Sasaki T., Timpl R., Fitzgerald J. J. Biol. Chem. 281:7341-7349(2006) · UniProtKB (2) · Mapped (14) |
| Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domain. McGillivray G., Savarirayan R., Cox T.C., Stojkoski C., McNeil R., Bankier A., Bateman J.F., Roscioli T., Gardner R.J.M., Lamande S.R. J. Med. Genet. 42:656-662(2005) · UniProtKB (1) |
| Mutations of COL10A1 in Schmid metaphyseal chondrodysplasia. Bateman J.F., Wilson R., Freddi S., Lamande S.R., Savarirayan R. |
| ADAMTS-1-knockout mice do not exhibit abnormalities in aggrecan turnover in vitro or in vivo. Little C.B., Mittaz L., Belluoccio D., Rogerson F.M., Campbell I.K., Meeker C.T., Bateman J.F., Pritchard M.A., Fosang A.J. Arthritis Rheum. 52:1461-1472(2005) · Mapped (6) |
| Misfolding of collagen X chains harboring Schmid metaphyseal chondrodysplasia mutations results in aberrant disulfide bond formation, intracellular retention, and activation of the unfolded protein response. Wilson R., Freddi S., Chan D., Cheah K.S., Bateman J.F. J. Biol. Chem. 280:15544-15552(2005) · Mapped (3) |
| Dominant collagen VI mutations are a common cause of Ullrich congenital muscular dystrophy. Baker N.L., Moergelin M., Peat R., Goemans N., North K.N., Bateman J.F., Lamande S.R. Hum. Mol. Genet. 14:279-293(2005) · UniProtKB (1) · Mapped (19) |
| Intracellular trafficking and degradation of unassociated proalpha2 chains of collagen type I. Gotkin M.G., Ripley C.R., Lamande S.R., Bateman J.F., Bienkowski R.S. Exp. Cell Res. 296:307-316(2004) · Mapped (12) |
| Is there an evolutionary relationship between WARP (von Willebrand factor A-domain-related protein) and the FACIT and FACIT-like collagens? Fitzgerald J., Bateman J.F. FEBS Lett. 552:91-94(2003) · Mapped (3) |