-
2
-
-
0001578843
-
Multiple sulfatase deficiency and the nature of the sulfatase family
-
(ed) Scriver CR, Beaudet AL (eds): New York: McGraw-Hill
-
Hopwood JJ, Ballabio A (ed): Multiple sulfatase deficiency and the nature of the sulfatase family; in Scriver CR, Beaudet AL (eds): The metabolic and molecular basis of inherited disease. New York: McGraw-Hill, 2001; 3, pp 3725-3732.
-
(2001)
The Metabolic and Molecular Basis of Inherited Disease
, vol.3
, pp. 3725-3732
-
-
Hopwood, J.J.1
Ballabio, A.2
-
3
-
-
0024166584
-
Metabolism of 3H-dehydroepiandrosterone sulphate by subjects with steroid sulphatase deficiency
-
Bergner E, Shapiro L: Metabolism of 3H-dehydroepiandrosterone sulphate by subjects with steroid sulphatase deficiency. J Inherit Metab Dis 1988; 11: 403-415.
-
(1988)
J. Inherit. Metab. Dis.
, vol.11
, pp. 403-415
-
-
Bergner, E.1
Shapiro, L.2
-
4
-
-
0002532563
-
Enzymological aspects of steroids conjugation
-
(ed) Bernstein S, Solomon S (eds): New York: McGraw-Hill
-
Roy AB (ed): Enzymological aspects of steroids conjugation; in Bernstein S, Solomon S (eds): Chemical and Biological Aspects of Steroid Conjugation,. New York: McGraw-Hill, 1970, p 74.
-
(1970)
Chemical and Biological Aspects of Steroid Conjugation
, pp. 74
-
-
Roy, A.B.1
-
5
-
-
0025253560
-
Phylogenetic conservation of arylsulfatases. cDNA cloning and expression of human arylsulfatase B
-
Peters C, Schmidt B, Rommerskirch W et al: Phylogenetic conservation of arylsulfatases. cDNA cloning and expression of human arylsulfatase B. J Biol Chem 1990; 265: 3374-3381.
-
(1990)
J. Biol. Chem.
, vol.265
, pp. 3374-3381
-
-
Peters, C.1
Schmidt, B.2
Rommerskirch, W.3
-
6
-
-
0029987932
-
Characterisation of a cluster of sulfatase genes on Xp22.3 suggests gene duplications in an ancestral pseudoautosomal region
-
Meroni G, Franco B, Archidiacono N et al: Characterisation of a cluster of sulfatase genes on Xp22.3 suggests gene duplications in an ancestral pseudoautosomal region. Hum Mol Genet 1996; 5: 423-431.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 423-431
-
-
Meroni, G.1
Franco, B.2
Archidiacono, N.3
-
7
-
-
0000497407
-
Metachromatic leukodystrophy
-
(ed) Scriver CR, Beaudet AL (eds): New York: McGraw-Hill
-
von Figura K, Gieselmann V, Jaeken J (ed): Metachromatic leukodystrophy; in Scriver CR, Beaudet AL (eds): ne methabolic and molecular basis of inherited disease. New York: McGraw-Hill, 2001; 3, pp 3695-3724.
-
(2001)
The Methabolic and Molecular Basis of Inherited Disease
, vol.3
, pp. 3695-3724
-
-
von Figura, K.1
Gieselmann, V.2
Jaeken, J.3
-
8
-
-
0001962515
-
Steroid sulfatase deficiency and X-linked ichthyosis
-
(ed): Scriver CR, Beaudet AL (eds): New York: McGraw-Hill
-
Ballabio A. Shapiro LJ (ed): Steroid sulfatase deficiency and X-linked ichthyosis; in Scriver CR, Beaudet AL (eds): The methabolic and molecular basis of inherited disease. New York: McGraw-Hill, 2001; 3, pp 4241-4262.
-
(2001)
The Methabolic and Molecular Basis of Inherited Disease
, vol.3
, pp. 4241-4262
-
-
Ballabio, A.1
Shapiro, L.J.2
-
10
-
-
0029130352
-
A novel amino acid modification in sulfatases that is defective in multiple sulfatase deficiency
-
Schmidt B, Selmer T, Ingendoh A, von Figura K: A novel amino acid modification in sulfatases that is defective in multiple sulfatase deficiency. Cell 1995; 82: 271-278.
-
(1995)
Cell
, vol.82
, pp. 271-278
-
-
Schmidt, B.1
Selmer, T.2
Ingendoh, A.3
von Figura, K.4
-
11
-
-
0028924667
-
A cluster of sulfatase genes on Xp22.3: Mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy
-
Franco B, Meroni G, Parenti G et al: A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy. Cell 1995; 81: 15-25.
-
(1995)
Cell
, vol.81
, pp. 15-25
-
-
Franco, B.1
Meroni, G.2
Parenti, G.3
-
12
-
-
0031568850
-
Structure of a human lysosomal sulfatase
-
Bond CS, Clements PR, Ashby SJ et al: Structure of a human lysosomal sulfatase. Structure 1997; 5: 277-289.
-
(1997)
Structure
, vol.5
, pp. 277-289
-
-
Bond, C.S.1
Clements, P.R.2
Ashby, S.J.3
-
13
-
-
0032539976
-
Crystal structure of human arylsulfatase A: The aldehyde function and the metal ion at the active site suggest a novel mechanism for sulfate ester hydrolysis
-
Lukatela G, Krauss N, Theis K et al: Crystal structure of human arylsulfatase A: the aldehyde function and the metal ion at the active site suggest a novel mechanism for sulfate ester hydrolysis. Biochemistry 1998; 37: 3654-3664.
-
(1998)
Biochemistry
, vol.37
, pp. 3654-3664
-
-
Lukatela, G.1
Krauss, N.2
Theis, K.3
-
14
-
-
0031172098
-
Identification by shotgun sequencing, genomic organization, and functional analysis of a fourth arylsulfatase gene (ARSF) from the Xp22.3 region
-
Puca AA, Zollo M, Repetto M et al: Identification by shotgun sequencing, genomic organization, and functional analysis of a fourth arylsulfatase gene (ARSF) from the Xp22.3 region. Genomics 1997; 42: 192-199.
-
(1997)
Genomics
, vol.42
, pp. 192-199
-
-
Puca, A.A.1
Zollo, M.2
Repetto, M.3
-
15
-
-
0029898602
-
The evolutionary conservation of a novel protein modification, the conversion of cysteine to serine-semialdehyde in arylsulfatase from Volvox carteri
-
Selmer T, Hallmann A, Schmidt B, Sumper M, von Figura K: The evolutionary conservation of a novel protein modification, the conversion of cysteine to serine-semialdehyde in arylsulfatase from Volvox carteri. Eur J Biochem 1996; 238: 341-345.
-
(1996)
Eur. J. Biochem.
, vol.238
, pp. 341-345
-
-
Selmer, T.1
Hallmann, A.2
Schmidt, B.3
Sumper, M.4
von Figura, K.5
|