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Results 21-30 of 41 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
1999
DECAY, a novel Drosophila caspase related to mammalian Caspase-3 and Caspase-7
Dorstyn, L.
;
Read, S.
;
Quinn, L.
;
Richardson, H.
;
Kumar, S.
1997
Ancient missense mutations in a new member of the RoRet gene family are likely to cause Familial Mediterranean Fever
Aksentijevich, I.
;
Centola, M.
;
Deng, Z.
;
Sood, R.
;
Balow, J.
;
Wood, G.
;
Zaks, N.
;
Mansfield, E.
;
Chen, X.
;
Eisenberg, S.
;
Vedula, A.
;
Shafran, N.
;
Raben, N.
;
Pras, E.
;
Pras, M.
;
Kastner, D.
;
Blake, T.
;
Baxevanis, A.
;
Robbins, C.
;
Krizman, D.
;
et al.
1999
Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes
McDermott, M.
;
Aksentijevich, I.
;
Galon, J.
;
McDermott, E.
;
Ogunkolade, B.
;
Centola, M.
;
Mansfield, E.
;
Gadina, M.
;
Karenko, L.
;
Petterson, T.
;
McCarthy, J.
;
Frucht, D.
;
Aringer, M.
;
Torosyan, Y.
;
Teppo, A.M.
;
Wilson, M.
;
Karaarslan, H.
;
Wan, Y.
;
Todd, I.
;
Wood, G.
;
et al.
1997
Pyruvate decarboxylase and anaerobic survival in Aspergillus nidulans
Lockington, R.
;
Borlace, G.
;
Kelly, J.
1997
Interspecies sequence differences in the Mip protein from the genus Legionella: implications for function and evolutionary relatedness
Ratcliff, R.
;
Donnellan, S.
;
Lanser, J.
;
Manning, P.
;
Heuzenroeder, M.
1996
A novel X-linked gene, G4.5. is responsible for Barth Syndrome
Bione, S.
;
D'Adamo, P.
;
Maestrini, E.
;
Gedeon, A.
;
Bolhuis, P.
;
Toniolo, D.
1996
Identification of the gene FMR2, associated with FRAXE mental retardation
Gecz, J.
;
Gedeon, A.
;
Sutherland, G.
;
Mulley, J.
1998
A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis.
Town, M.
;
Jean, G.
;
Cherqui, S.
;
Attard, M.
;
Forestier, L.
;
Whitmore, S.
;
Callen, D.
;
Gribouval, O.
;
Broyer, M.
;
Bates, G.
;
van't Hoff, W.
;
Antignac, C.
1999
Genomic structure and expression analysis of the spastic paraplegia gene, SPG7
Settasatian, C.
;
Whitmore, S.
;
Crawford, J.
;
Bilton, R.
;
Cleton-Jansen, A.M.
;
Sutherland, G.
;
Callen, D.
1998
PAK3 mutation in nonsyndromic X-linked mental retardation
Allen, K.
;
Gleeson, J.
;
Bagrodia, S.
;
Partington, M.
;
MacMillan, J.
;
Cerione, R.
;
Mulley, J.
;
Walsh, C.
Discover
Author
8
Mulley, J.
7
Callen, D.
7
Sutherland, G.
5
Doggett, N.
5
Gecz, J.
5
Timmis, J.
5
Whitmore, S.
4
Aksentijevich, I.
4
Centola, M.
4
Cleton-Jansen, A.M.
.
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Subject
26
Humans
25
Amino Acid Sequence
25
Base Sequence
17
Cloning, Molecular
14
Sequence Homology, Amino Acid
13
Animals
13
Female
13
Male
9
DNA, Complementary
9
Mutation
.
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Date issued
12
1999
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1998
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1997
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1996
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1992