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Results 1-10 of 11 (Search time: 0.004 seconds).
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Issue Date
Title
Author(s)
2000
FMR3 is a novel gene associated with FRAXE CpG island and transcriptionally silent in FRAXE full mutations
Gecz, J.
2007
Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a marfanoid habitus
Raymond, F.
;
Tarpey, P.
;
Edkins, S.
;
Tofts, C.
;
O'Meara, S.
;
Teague, J.
;
Butler, A.
;
Stevens, C.
;
Barthorpe, S.
;
Buck, G.
;
Cole, J.
;
Dicks, E.
;
Gray, K.
;
Harrison, R.
;
Hills, K.
;
Hinton, J.
;
Jones, D.
;
Menzies, A.
;
Perry, J.
;
Raine, K.
;
et al.
2005
Drosophila starvin encodes a tissue-specific BAG-domain protein required for larval food uptake
Coulson, M.
;
Robert, S.
;
Saint, R.
2001
A recurrent RNA-splicing mutation in the SEDL gene causes X-linked spondyloepiphyseal dysplasia tarda
Tiller, G.
;
Hannig, V.
;
Dozier, D.
;
Carrel, L.
;
Trevarthen, K.
;
Wilcox, W.
;
Mundlos, S.
;
Haines, J.
;
Gedeon, A.
;
Gecz, J.
2008
Interference with splicing of Presenilin transcripts has potent dominant negative effects on Presenilin activity
Nornes, S.
;
Newman, M.
;
Verdile, G.
;
Wells, S.
;
Stoick-Cooper, C.
;
Tucker, B.
;
Frederich-Sleptsova, I.
;
Martins, R.
;
Lardelli, M.
2001
The molecular basis of X-linked spondyloepiphyseal dysplasia tarda
Gedeon, A.
;
Tiller, G.
;
Le Merrer, M.
;
Heuertz, S.
;
Tranebjaerg, L.
;
Chitayat, D.
;
Robertson, S.
;
Glass, I.
;
Savarirayan, R.
;
Cole, W.
;
Rimoin, D.
;
Kousseff, B.
;
Ohashi, H.
;
Zabel, B.
;
Munnich, A.
;
Gecz, J.
;
Mulley, J.
1999
Sanfilippo type B syndrome (mucopolysaccharidosis III B): allelic heterogeneity corresponds to the wide spectrum of clinical phenotypes
Weber, B.
;
Guo, X.H.
;
Kleijer, W.
;
van de Kamp, J.
;
Poorthuis, B.
;
Hopwood, J.
1996
Stable inheritance of an HLA-"blank" phenotype associated with a structural mutation in the HLA-A*0301 gene
Lienert, K.
;
Russ, G.
;
Lester, S.
;
Bennet, G.
;
Gao, X.
;
McCluskey, J.
2003
Pex13 inactivation in the mouse disrupts peroxisome biogenesis and leads to a Zellweger syndrome phenotype
Maxwell, M.
;
Bjorkman, J.
;
Nguyen, T.
;
Sharp, P.
;
Finnie, J.
;
Paterson, C.
;
Tonks, I.
;
Paton, B.
;
Kay, G.
;
Crane, D.
2013
EAT1 promotes tapetal cell death by regulating aspartic proteases during male reproductive development in rice
Niu, N.
;
Liang, W.
;
Yang, X.
;
Jin, W.
;
Wilson, Z.
;
Hu, J.
;
Zhang, D.
Discover
Author
3
Gecz, J.
2
Gedeon, A.
2
Liang, W.
2
Tiller, G.
2
Zhang, D.
1
Barthorpe, S.
1
Bennet, G.
1
Bjorkman, J.
1
Buck, G.
1
Butler, A.
.
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Subject
9
Molecular Sequence Data
7
Humans
4
Amino Acid Sequence
4
Animals
4
Exons
4
Male
3
Genetic Linkage
3
Pedigree
3
Reverse Transcriptase Polymerase ...
3
RNA, Messenger
.
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Date issued
2
2010 - 2013
7
2000 - 2009
2
1996 - 1999