Sequence of SUIS_HUMAN

oligo-1,6-glucosidase

P14410

1827

209453

sucrose alpha-glucosidase

P14410

1827

209453

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Chantret I.,Lacasa M.,Chevalier G.,Ruf J.,Islam I.,Mantei N.,Edwards Y.,Swallow D.,Rousset M.

Sequence of the complete cDNA and the 5' structure of the human sucrase-isomaltase gene. Possible homology with a yeast glucoamylase.

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The DNA sequence, annotation and analysis of human chromosome 3.

Nature

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1259235

The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

Genome Res.

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2004

1259236

Green F.,Edwards Y.,Hauri H.-P.,Povey S.,Ho M.W.,Pinto M.,Swallow D.

Isolation of a cDNA probe for a human jejunal brush-border hydrolase, sucrase-isomaltase, and assignment of the gene locus to chromosome 3.

Gene

57

101-110

1987

1259237

Gorvel J.P.,Ferrero A.,Chambraud L.,Rigal A.,Bonicel J.,Maroux S.

Expression of sucrase-isomaltase and dipeptidylpeptidase IV in human small intestine and colon.

Gastroenterology

101

618-625

1991

1259238

Keller P.,Semenza G.,Shaltiel S.

Phosphorylation of the N-terminal intracellular tail of sucrase-isomaltase by cAMP-dependent protein kinase.

Eur. J. Biochem.

233

963-968

1995

1259239

Sim L.,Willemsma C.,Mohan S.,Naim H.Y.,Pinto B.M.,Rose D.R.

Structural basis for substrate selectivity in human maltase-glucoamylase and sucrase-isomaltase N-terminal domains.

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2010

1259240

Ouwendijk J.,Moolenaar C.E.C.,Peters W.J.,Hollenberg C.P.,Ginsel L.A.,Fransen J.A.M.,Naim H.Y.

Congenital sucrase-isomaltase deficiency: identification of a glutamine to proline substitution that leads to a transport block of sucrase-isomaltase in a pre-Golgi compartment.

J. Clin. Invest.

97

633-641

1996

1259241

Jacob R.,Zimmer K.P.,Schmitz J.,Naim H.Y.

Congenital sucrase-isomaltase deficiency arising from cleavage and secretion of a mutant form of the enzyme.

J. Clin. Invest.

106

281-287

2000

1259242

Spodsberg N.,Jacob R.,Alfalah M.,Zimmer K.P.,Naim H.Y.

Molecular basis of aberrant apical protein transport in an intestinal enzyme disorder.

J. Biol. Chem.

276

23506-23510

2001

1259243

Ritz V.,Alfalah M.,Zimmer K.P.,Schmitz J.,Jacob R.,Naim H.Y.

Congenital sucrase-isomaltase deficiency because of an accumulation of the mutant enzyme in the endoplasmic reticulum.

Gastroenterology

125

1678-1685

2003

1259244

Sander P.,Alfalah M.,Keiser M.,Korponay-Szabo I.,Kovacs J.B.,Leeb T.,Naim H.Y.

Novel mutations in the human sucrase-isomaltase gene (SI) that cause congenital carbohydrate malabsorption.

Hum. Mutat.

27

119-119

2006