-
1
-
-
23944518940
-
Molecular etiology of primary hyperoxaluria type 1: New directions for treatment
-
DOI 10.1159/000086362
-
C.J. Danpure Molecular etiology of primary hyperoxaluria type 1: new directions for treatment Am. J. Nephrol. 25 2005 303 310 (Pubitemid 41202755)
-
(2005)
American Journal of Nephrology
, vol.25
, Issue.3
, pp. 303-310
-
-
Danpure, C.J.1
-
2
-
-
26444485692
-
Primary hyperoxaluria: From gene defects to designer drugs?
-
DOI 10.1093/ndt/gfh923
-
C.J. Danpure Primary hyperoxaluria: from gene defects to designer drugs? Nephrol. Dial. Transplant. 20 2005 1525 1529 (Pubitemid 41418571)
-
(2005)
Nephrology Dialysis Transplantation
, vol.20
, Issue.8
, pp. 1525-1529
-
-
Danpure, C.J.1
-
3
-
-
10944220190
-
Pyridoxamine lowers kidney crystals in experimental hyperoxaluria: A potential therapy for primary hyperoxaluria
-
DOI 10.1111/j.1523-1755.2005.00054.x
-
S.V. Chetyrkin, D. Kim, J.M. Belmont, J.I. Scheinman, B.G. Hudson, and P.A. Voziyan Pyridoxamine lowers kidney crystals in experimental hyperoxaluria: a potential therapy for primary hyperoxaluria Kidney Int. 67 2005 53 60 (Pubitemid 40019225)
-
(2005)
Kidney International
, vol.67
, Issue.1
, pp. 53-60
-
-
Chetyrkin, S.V.1
Kim, D.2
Belmont, J.M.3
Scheinman, J.I.4
Hudson, B.G.5
Voziyan, P.A.6
-
4
-
-
0025760316
-
Characterization and chromosomal mapping of a genomic clone encoding human alanine:glyoxylate aminotransferase
-
P.E. Purdue, M.J. Lumb, M. Fox, G. Griffo, C. Hamon-Benais, S. Povey, and C.J. Danpure Characterization and chromosomal mapping of a genomic clone encoding human alanine:glyoxylate aminotransferase Genomics 10 1991 34 42
-
(1991)
Genomics
, vol.10
, pp. 34-42
-
-
Purdue, P.E.1
Lumb, M.J.2
Fox, M.3
Griffo, G.4
Hamon-Benais, C.5
Povey, S.6
Danpure, C.J.7
-
5
-
-
0025640818
-
Identification of mutations associated with peroxisome-to-mitochondrion mistargeting of alanine/glyoxylate aminotransferase in primary hyperoxaluria type 1
-
P.E. Purdue, Y. Takada, and C.J. Danpure Identification of mutations associated with peroxisome-to-mitochondrion mistargeting of alanine/glyoxylate aminotransferase in primary hyperoxaluria type 1 J. Cell Biol. 111 1990 2341 2351 (Pubitemid 120014519)
-
(1990)
Journal of Cell Biology
, vol.111
, Issue.6 PART 1
, pp. 2341-2351
-
-
Purdue, P.E.1
Takada, Y.2
Danpure, C.J.3
-
6
-
-
0025778863
-
An intronic duplication in the alanine: Glyoxylate aminotransferase gene facilitates identification of mutations in compound heterozygote patients with primary hyperoxaluria type 1
-
P.E. Purdue, M.J. Lumb, J. Allsop, and C.J. Danpure An intronic duplication in the alanine: glyoxylate aminotransferase gene facilitates identification of mutations in compound heterozygote patients with primary hyperoxaluria type 1 Hum. Genet. 87 1991 394 396
-
(1991)
Hum. Genet.
, vol.87
, pp. 394-396
-
-
Purdue, P.E.1
Lumb, M.J.2
Allsop, J.3
Danpure, C.J.4
-
7
-
-
0033575214
-
Effect of N-terminal alpha-helix formation on the dimerization and intracellular targeting of alanine:glyoxylate aminotransferase
-
M.J. Lumb, A.F. Drake, and C.J. Danpure Effect of N-terminal alpha-helix formation on the dimerization and intracellular targeting of alanine:glyoxylate aminotransferase J. Biol. Chem. 274 1999 20587 20596
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 20587-20596
-
-
Lumb, M.J.1
Drake, A.F.2
Danpure, C.J.3
-
8
-
-
0025746324
-
Mistargeting of peroxisomal L-alanine:glyoxylate aminotransferase to mitochondria in primary hyperoxaluria patients depends upon activation of a cryptic mitochondrial targeting sequence by a point mutation
-
P.E. Purdue, J. Allsop, G. Isaya, L.E. Rosenberg, and C.J. Danpure Mistargeting of peroxisomal L-alanine:glyoxylate aminotransferase to mitochondria in primary hyperoxaluria patients depends upon activation of a cryptic mitochondrial targeting sequence by a point mutation Proc. Natl Acad. Sci. USA 88 1991 10900 10904 (Pubitemid 21915946)
-
(1991)
Proceedings of the National Academy of Sciences of the United States of America
, vol.88
, Issue.23
, pp. 10900-10904
-
-
Purdue, P.E.1
Allsop, J.2
Isaya, G.3
Rosenberg, L.E.4
Danpure, C.J.5
-
9
-
-
0034680869
-
Functional synergism between the most common polymorphism in human alanine:glyoxylate aminotransferase and four of the most common disease-causing mutations
-
M.J. Lumb, and C.J. Danpure Functional synergism between the most common polymorphism in human alanine:glyoxylate aminotransferase and four of the most common disease-causing mutations J. Biol. Chem. 275 2000 36415 36422
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 36415-36422
-
-
Lumb, M.J.1
Danpure, C.J.2
-
10
-
-
66349125901
-
Primary hyperoxaluria type 1: Update and additional mutation analysis of the AGXT gene
-
E.L. Williams, C. Acquaviva, A. Amoroso, F. Chevalier, M. Coulter-Mackie, C.G. Monico, D. Giachino, T. Owen, A. Robbiano, E. Salido, H. Waterham, and G. Rumsby Primary hyperoxaluria type 1: update and additional mutation analysis of the AGXT gene Hum. Mutat. 30 2009 910 917
-
(2009)
Hum. Mutat.
, vol.30
, pp. 910-917
-
-
Williams, E.L.1
Acquaviva, C.2
Amoroso, A.3
Chevalier, F.4
Coulter-Mackie, M.5
Monico, C.G.6
Giachino, D.7
Owen, T.8
Robbiano, A.9
Salido, E.10
Waterham, H.11
Rumsby, G.12
-
11
-
-
7544241975
-
Molecular aetiology of primary hyperoxaluria type 1
-
C.J. Danpure Molecular aetiology of primary hyperoxaluria type 1 Nephron Exp. Nephrol. 98 2004 e39 e44
-
(2004)
Nephron Exp. Nephrol.
, vol.98
-
-
Danpure, C.J.1
-
12
-
-
0042242590
-
Crystal structure of alanine:glyoxylate aminotransferase and the relationship between genotype and enzymatic phenotype in primary hyperoxaluria type 1
-
DOI 10.1016/S0022-2836(03)00791-5
-
X. Zhang, S.M. Roe, Y. Hou, M. Bartlam, Z. Rao, L.H. Pearl, and C.J. Danpure Crystal structure of alanine:glyoxylate aminotransferase and the relationship between genotype and enzymatic phenotype in primary hyperoxaluria type 1 J. Mol. Biol. 331 2003 643 652 (Pubitemid 36937151)
-
(2003)
Journal of Molecular Biology
, vol.331
, Issue.3
, pp. 643-652
-
-
Zhang, X.1
Roe, S.M.2
Hou, Y.3
Bartlam, M.4
Rao, Z.5
Pearl, L.H.6
Danpure, C.J.7
-
13
-
-
36349021899
-
Human wild-type alanine:glyoxylate aminotransferase and its naturally occurring G82E variant: Functional properties and physiological implications
-
DOI 10.1042/BJ20070637
-
B. Cellini, M. Bertoldi, R. Montioli, A. Paiardini, and C. Borri Voltattorni Human wild-type alanine:glyoxylate aminotransferase and its naturally occurring G82E variant: functional properties and physiological implications Biochem. J. 408 2007 39 50 (Pubitemid 350158401)
-
(2007)
Biochemical Journal
, vol.408
, Issue.1
, pp. 39-50
-
-
Cellini, B.1
Bertoldi, M.2
Montioli, R.3
Paiardini, A.4
Borri Voltattorni, C.5
-
14
-
-
78649899924
-
Human liver peroxisomal alanine:glyoxylate aminotransferase: Different stability under chemical stress of the major allele, the minor allele, and its pathogenic G170R variant
-
B. Cellini, A. Lorenzetto, R. Montioli, E. Oppici, and C.B. Voltattorni Human liver peroxisomal alanine:glyoxylate aminotransferase: different stability under chemical stress of the major allele, the minor allele, and its pathogenic G170R variant Biochimie 92 2010 1801 1811
-
(2010)
Biochimie
, vol.92
, pp. 1801-1811
-
-
Cellini, B.1
Lorenzetto, A.2
Montioli, R.3
Oppici, E.4
Voltattorni, C.B.5
-
15
-
-
77649267180
-
Molecular defects of the glycine 41 variants of alanine glyoxylate aminotransferase associated with primary hyperoxaluria type i
-
B. Cellini, R. Montioli, A. Paiardini, A. Lorenzetto, F. Maset, T. Bellini, E. Oppici, and C.B. Voltattorni Molecular defects of the glycine 41 variants of alanine glyoxylate aminotransferase associated with primary hyperoxaluria type I Proc. Natl Acad. Sci. USA 107 2010 2896 2901
-
(2010)
Proc. Natl Acad. Sci. USA
, vol.107
, pp. 2896-2901
-
-
Cellini, B.1
Montioli, R.2
Paiardini, A.3
Lorenzetto, A.4
Maset, F.5
Bellini, T.6
Oppici, E.7
Voltattorni, C.B.8
-
16
-
-
67649732393
-
Molecular insight into the synergism between the minor allele of human liver peroxisomal alanine:glyoxylate aminotransferase and the F152I mutation
-
B. Cellini, R. Montioli, A. Paiardini, A. Lorenzetto, and C.B. Voltattorni Molecular insight into the synergism between the minor allele of human liver peroxisomal alanine:glyoxylate aminotransferase and the F152I mutation J. Biol. Chem. 284 2009 8349 8358
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 8349-8358
-
-
Cellini, B.1
Montioli, R.2
Paiardini, A.3
Lorenzetto, A.4
Voltattorni, C.B.5
-
17
-
-
40449128475
-
Construction, purification and characterization of untagged human liver alanine-glyoxylate aminotransferase expressed in Escherichia coli
-
B. Cellini, R. Montioli, S. Bianconi, J.P. Lopez-Alonso, and C.B. Voltattorni Construction, purification and characterization of untagged human liver alanine-glyoxylate aminotransferase expressed in Escherichia coli Protein Pept. Lett. 15 2008 153 159 (Pubitemid 351346469)
-
(2008)
Protein and Peptide Letters
, vol.15
, Issue.2
, pp. 153-159
-
-
Cellini, B.1
Montioli, R.2
Bianconi, S.3
Lopez-Alonso, J.P.4
Voltattorni, C.B.5
-
18
-
-
0031869580
-
Structural characteristics of brain glutamate decarboxylase in relation to its interaction and activation
-
DOI 10.1006/abbi.1997.0457
-
C.H. Chen, S.J. Wu, and D.L. Martin Structural characteristics of brain glutamate decarboxylase in relation to its interaction and activation Arch. Biochem. Biophys. 349 1998 175 182 (Pubitemid 28368404)
-
(1998)
Archives of Biochemistry and Biophysics
, vol.349
, Issue.1
, pp. 175-182
-
-
Chen, C.-H.1
Wu, S.J.2
Martin, D.L.3
-
19
-
-
0028100451
-
Acid-induced reversible unfolding of mitochondrial aspartate aminotransferase
-
A. Artigues, A. Iriarte, and M. Martinez-Carrion Acid-induced reversible unfolding of mitochondrial aspartate aminotransferase J. Biol. Chem. 269 1994 21990 21999 (Pubitemid 24282118)
-
(1994)
Journal of Biological Chemistry
, vol.269
, Issue.35
, pp. 21990-21999
-
-
Artigues, A.1
Iriarte, A.2
Martinez-Carrion, M.3
-
20
-
-
0032560031
-
Reversible unfolding of sheep liver tetrameric serine hydroxymethyltransferase
-
DOI 10.1016/S0167-4838(98)00013-2, PII S0167483898000132
-
B. Venkatesha, J.B. Udgaonkar, N.A. Rao, and H.S. Savithri Reversible unfolding of sheep liver tetrameric serine hydroxymethyltransferase Biochim. Biophys. Acta 1384 1998 141 152 (Pubitemid 28193024)
-
(1998)
Biochimica et Biophysica Acta - Protein Structure and Molecular Enzymology
, vol.1384
, Issue.1
, pp. 141-152
-
-
Venkatesha, B.1
Udgaonkar, J.B.2
Rao, N.A.3
Savithri, H.S.4
-
21
-
-
0015829898
-
The tryptophanase from Escherichia coli K-12. II. Comparison of the thermal stabilities of apo-, holo-, and hybrid enzymes
-
O. Raibaud, and M.E. Goldberg The tryptophanase from Escherichia coli K-12. II. Comparison of the thermal stabilities of apo-, holo-, and hybrid enzymes J. Biol. Chem. 248 1973 3451 3455
-
(1973)
J. Biol. Chem.
, vol.248
, pp. 3451-3455
-
-
Raibaud, O.1
Goldberg, M.E.2
-
22
-
-
0029885703
-
2 subunit probed by the spectroscopic properties of pyridoxal phosphate and by enzymatic activity
-
DOI 10.1074/jbc.271.15.8612
-
S.A. Ahmed, P. McPhie, and E.W. Miles A thermally induced reversible conformational transition of the tryptophan synthase beta2 subunit probed by the spectroscopic properties of pyridoxal phosphate and by enzymatic activity J. Biol. Chem. 271 1996 8612 8617 (Pubitemid 26123275)
-
(1996)
Journal of Biological Chemistry
, vol.271
, Issue.15
, pp. 8612-8617
-
-
Ahmed, S.A.1
McPhie, P.2
Miles, E.W.3
-
23
-
-
0034704154
-
Role of pyridoxal 5′-phosphate in the structural stabilization of O-acetylserine sulfhydrylase
-
DOI 10.1074/jbc.M007015200
-
S. Bettati, S. Benci, B. Campanini, S. Raboni, G. Chirico, S. Beretta, K.D. Schnackerz, T.L. Hazlett, E. Gratton, and A. Mozzarelli Role of pyridoxal 5′-phosphate in the structural stabilization of O-acetylserine sulfhydrylase J. Biol. Chem. 275 2000 40244 40251 (Pubitemid 32064655)
-
(2000)
Journal of Biological Chemistry
, vol.275
, Issue.51
, pp. 40244-40251
-
-
Bettati, S.1
Benci, S.2
Campanini, B.3
Raboni, S.4
Chirico, G.5
Beretta, S.6
Schnackerz, K.D.7
Hazlett, T.L.8
Gratton, E.9
Mozzarelli, A.10
-
24
-
-
0027437588
-
Dissociation, unfolding and refolding trials of pig kidney 3,4-dihydroxyphenylalanine (Dopa) decarboxylase
-
P. Dominici, P.S. Moore, and C. Borri Voltattorni Dissociation, unfolding and refolding trials of pig kidney 3, 4-dihydroxyphenylalanine (dopa) decarboxylase Biochem. J. 295 Pt 2 1993 493 500 (Pubitemid 23315189)
-
(1993)
Biochemical Journal
, vol.295
, Issue.2
, pp. 493-500
-
-
Dominici, P.1
Moore, P.S.2
Voltattorni, C.B.3
-
25
-
-
0029910143
-
Structural studies on folding intermediates of serine hydroxymethyltransferase using fluorescence resonance energy transfer
-
DOI 10.1074/jbc.271.44.27311
-
K. Cai, and V. Schirch Structural studies on folding intermediates of serine hydroxymethyltransferase using fluorescence resonance energy transfer J. Biol. Chem. 271 1996 27311 27320 (Pubitemid 26367285)
-
(1996)
Journal of Biological Chemistry
, vol.271
, Issue.44
, pp. 27311-27320
-
-
Cai, K.1
Schirch, V.2
-
26
-
-
57649183376
-
In vivo and in vitro examination of stability of primary hyperoxaluria-associated human alanine:glyoxylate aminotransferase
-
E.D. Hopper, A.M. Pittman, M.C. Fitzgerald, and C.L. Tucker In vivo and in vitro examination of stability of primary hyperoxaluria-associated human alanine:glyoxylate aminotransferase J. Biol. Chem. 283 2008 30493 30502
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 30493-30502
-
-
Hopper, E.D.1
Pittman, A.M.2
Fitzgerald, M.C.3
Tucker, C.L.4
-
27
-
-
0026552823
-
A glycine-to-glutamate substitution abolishes alanine:glyoxylate aminotransferase catalytic activity in a subset of patients with primary hyperoxaluria type 1
-
P.E. Purdue, M.J. Lumb, J. Allsop, Y. Minatogawa, and C.J. Danpure A glycine-to-glutamate substitution abolishes alanine:glyoxylate aminotransferase catalytic activity in a subset of patients with primary hyperoxaluria type 1 Genomics 13 1992 215 218
-
(1992)
Genomics
, vol.13
, pp. 215-218
-
-
Purdue, P.E.1
Lumb, M.J.2
Allsop, J.3
Minatogawa, Y.4
Danpure, C.J.5
-
28
-
-
0027378530
-
Enzymological and mutational analysis of a complex primary hyperoxaluria type I phenotype involving alanine:glyoxylate aminotransferase peroxisome- to-mitochondrion mistargeting and intraperoxisomal aggregation
-
C.J. Danpure, P.E. Purdue, P. Fryer, S. Griffiths, J. Allsop, M.J. Lumb, K.M. Guttridge, P.R. Jennings, J.I. Scheinman, and S.M. Mauer Enzymological and mutational analysis of a complex primary hyperoxaluria type 1 phenotype involving alanine:glyoxylate aminotransferase peroxisome-to-mitochondrion mistargeting and intraperoxisomal aggregation Am. J. Hum. Genet. 53 1993 417 432 (Pubitemid 23308936)
-
(1993)
American Journal of Human Genetics
, vol.53
, Issue.2
, pp. 417-432
-
-
Danpure, C.J.1
Purdue, P.E.2
Fryer, P.3
Griffiths, S.4
Allsop, J.5
Lumb, M.J.6
Guttridge, K.M.7
Jennings, P.R.8
Scheinman, J.I.9
Mauer, S.M.10
Davidson, N.O.11
-
29
-
-
17744370337
-
Pyridoxine effect in type I primary hyperoxaluria is associated with the most common mutant allele
-
DOI 10.1111/j.1523-1755.2005.00267.x
-
C.G. Monico, S. Rossetti, J.B. Olson, and D.S. Milliner Pyridoxine effect in type I primary hyperoxaluria is associated with the most common mutant allele Kidney Int. 67 2005 1704 1709 (Pubitemid 40577704)
-
(2005)
Kidney International
, vol.67
, Issue.5
, pp. 1704-1709
-
-
Monico, C.G.1
Rossetti, S.2
Olson, J.B.3
Milliner, D.S.4
-
30
-
-
0023688254
-
Further studies on the activity and subcellular distribution of alanine:glyoxylate aminotransferase in the livers of patients with primary hyperoxaluria type 1
-
C.J. Danpure, and P.R. Jennings Further studies on the activity and subcellular distribution of alanine:glyoxylate aminotransferase in the livers of patients with primary hyperoxaluria type 1 Clin. Sci. Lond 75 1988 315 322
-
(1988)
Clin. Sci. Lond
, vol.75
, pp. 315-322
-
-
Danpure, C.J.1
Jennings, P.R.2
-
31
-
-
0029046782
-
Modeling of the spatial structure of eukaryotic ornithine decarboxylases
-
N.V. Grishin, M.A. Phillips, and E.J. Goldsmith Modeling of the spatial structure of eukaryotic ornithine decarboxylases Protein Sci. 4 1995 1291 1304
-
(1995)
Protein Sci.
, vol.4
, pp. 1291-1304
-
-
Grishin, N.V.1
Phillips, M.A.2
Goldsmith, E.J.3
-
32
-
-
0034829759
-
AGXT gene mutations and their influence on clinical heterogeneity of type 1 primary hyperoxaluria
-
A. Amoroso, D. Pirulli, F. Florian, D. Puzzer, M. Boniotto, S. Crovella, S. Zezlina, A. Spano, G. Mazzola, S. Savoldi, C. Ferrettini, S. Berutti, M. Petrarulo, and M. Marangella AGXT gene mutations and their influence on clinical heterogeneity of type 1 primary hyperoxaluria J. Am. Soc. Nephrol. 12 2001 2072 2079 (Pubitemid 32880343)
-
(2001)
Journal of the American Society of Nephrology
, vol.12
, Issue.10
, pp. 2072-2079
-
-
Amoroso, A.1
Pirulli, D.2
Florian, F.3
Puzzer, D.4
Boniotto, M.5
Crovella, S.6
Zezlina, S.7
Spano, A.8
Mazzola, G.9
Savoldi, S.10
Ferrettini, C.11
Berutti, S.12
Petrarulo, M.13
Marangella, M.14
-
33
-
-
0035197206
-
Three novel deletions in the alanine: Glyoxylate aminotransferase gene of three patients with type 1 hyperoxaluria
-
DOI 10.1006/mgme.2001.3222
-
M.B. Coulter-Mackie, G. Rumsby, D.A. Applegarth, and J.R. Toone Three novel deletions in the alanine:glyoxylate aminotransferase gene of three patients with type 1 hyperoxaluria Mol. Genet. Metab. 74 2001 314 321 (Pubitemid 33111911)
-
(2001)
Molecular Genetics and Metabolism
, vol.74
, Issue.3
, pp. 314-321
-
-
Coulter-Mackie, M.B.1
Rumsby, G.2
Applegarth, D.A.3
Toone, J.R.4
-
34
-
-
3242779378
-
Clinical implications of mutation analysis in primary hyperoxaluria type 1
-
DOI 10.1111/j.1523-1755.2004.00796.x
-
C.S. van Woerden, J.W. Groothoff, F.A. Wijburg, C. Annink, R.J. Wanders, and H.R. Waterham Clinical implications of mutation analysis in primary hyperoxaluria type 1 Kidney Int. 66 2004 746 752 (Pubitemid 38982018)
-
(2004)
Kidney International
, vol.66
, Issue.2
, pp. 746-752
-
-
Van Woerden, C.S.1
Groothoff, J.W.2
Wijburg, F.A.3
Annink, C.4
Wanders, R.J.A.5
Waterham, H.R.6
-
35
-
-
20844462725
-
Implications of genotype and enzyme phenotype in pyridoxine response of patients with type i primary hyperoxaluria
-
C.G. Monico, J.B. Olson, and D.S. Milliner Implications of genotype and enzyme phenotype in pyridoxine response of patients with type I primary hyperoxaluria Am. J. Nephrol. 25 2005 183 188
-
(2005)
Am. J. Nephrol.
, vol.25
, pp. 183-188
-
-
Monico, C.G.1
Olson, J.B.2
Milliner, D.S.3
-
36
-
-
44649134535
-
Partial trypsin digestion as an indicator of mis-folding of mutant alanine:glyoxylate aminotransferase and chaperone effects of specific ligands. Study of a spectrum of missense mutants
-
M.B. Coulter-Mackie, and Q. Lian Partial trypsin digestion as an indicator of mis-folding of mutant alanine:glyoxylate aminotransferase and chaperone effects of specific ligands. Study of a spectrum of missense mutants Mol. Genet. Metab. 94 2008 368 374
-
(2008)
Mol. Genet. Metab.
, vol.94
, pp. 368-374
-
-
Coulter-Mackie, M.B.1
Lian, Q.2
-
37
-
-
33845288635
-
Primary hyperoxaluria type 1: AGT mistargeting highlights the fundamental differences between the peroxisomal and mitochondrial protein import pathways
-
DOI 10.1016/j.bbamcr.2006.08.021, PII S0167488906002291, Peroxisomes: Morphology, Function, Biogenesis and Disorders
-
C.J. Danpure Primary hyperoxaluria type 1: AGT mistargeting highlights the fundamental differences between the peroxisomal and mitochondrial protein import pathways Biochim. Biophys. Acta 1763 2006 1776 1784 (Pubitemid 44880464)
-
(2006)
Biochimica et Biophysica Acta - Molecular Cell Research
, vol.1763
, Issue.12
, pp. 1776-1784
-
-
Danpure, C.J.1
-
38
-
-
0032778022
-
Molecular analysis of hyperoxaluria type 1 in Italian patients reveals eight new mutations in the alanine:glyoxylate aminotransferase gene
-
DOI 10.1007/s004390050998
-
D. Pirulli, D. Puzzer, L. Ferri, S. Crovella, A. Amoroso, C. Ferrettini, M. Marangella, G. Mazzola, and F. Florian Molecular analysis of hyperoxaluria type 1 in Italian patients reveals eight new mutations in the alanine: glyoxylate aminotransferase gene Hum. Genet. 104 1999 523 525 (Pubitemid 29370930)
-
(1999)
Human Genetics
, vol.104
, Issue.6
, pp. 523-525
-
-
Pirulli, D.1
Puzzer, D.2
Ferri, L.3
Crovella, S.4
Amoroso, A.5
Ferrettini, C.6
Marangella, M.7
Mazzola, G.8
Florian, F.9
-
39
-
-
33750628757
-
Consequences of missense mutations for dimerization and turnover of alanine:glyoxylate aminotransferase: Study of a spectrum of mutations
-
DOI 10.1016/j.ymgme.2006.07.013, PII S1096719206002794
-
M.B. Coulter-Mackie, and Q. Lian Consequences of missense mutations for dimerization and turnover of alanine:glyoxylate aminotransferase: study of a spectrum of mutations Mol. Genet. Metab. 89 2006 349 359 (Pubitemid 44692542)
-
(2006)
Molecular Genetics and Metabolism
, vol.89
, Issue.4
, pp. 349-359
-
-
Coulter-Mackie, M.B.1
Lian, Q.2
-
40
-
-
15744378364
-
Overexpression of human alanine:glyoxylate aminotransferase in Escherichia coli: Renaturation from guanidine-HCl and affinity for pyridoxal phosphate co-factor
-
DOI 10.1016/j.pep.2004.11.004
-
M.B. Coulter-Mackie, Q. Lian, and S.G. Wong Overexpression of human alanine:glyoxylate aminotransferase in Escherichia coli: renaturation from guanidine-HCl and affinity for pyridoxal phosphate co-factor Protein Expr. Purif. 41 2005 18 26 (Pubitemid 40406359)
-
(2005)
Protein Expression and Purification
, vol.41
, Issue.1
, pp. 18-26
-
-
Coulter-Mackie, M.B.1
Lian, Q.2
Wong, S.G.3
-
42
-
-
0032793206
-
Determining subunit dissociation constants in natural and recombinant proteins
-
DOI 10.1016/S0076-6879(99)06008-5
-
L.R. Manning, A. Dumoulin, W.T. Jenkins, R.M. Winslow, and J.M. Manning Determining subunit dissociation constants in natural and recombinant proteins Meth. Enzymol. 306 1999 113 129 (Pubitemid 29356827)
-
(1999)
Methods in Enzymology
, vol.306
, pp. 113-129
-
-
Manning, L.R.1
Dumoulin, A.2
Jenkins, W.T.3
Winslow, R.M.4
Manning, J.M.5
-
43
-
-
0027136282
-
Comparative protein modelling by satisfaction of spatial restraints
-
DOI 10.1006/jmbi.1993.1626
-
A. Sali, and T.L. Blundell Comparative protein modelling by satisfaction of spatial restraints J. Mol. Biol. 234 1993 779 815 (Pubitemid 24007801)
-
(1993)
Journal of Molecular Biology
, vol.234
, Issue.3
, pp. 779-815
-
-
Sali, A.1
Blundell, T.L.2
|