Reactome: A Curated Pathway Database

Query author contributions in Reactome

Reactome depends on collaboration between our curation team and outside experts to assemble and peer-review its pathway modules. The integration of ORCID within Reactome enables us to meet a key challenge with authoring, curating and reviewing biological information by incentivizing and crediting the external experts that contribute their expertise and time to the Reactome curation process. More information is available at ORCID and Reactome.

If you have an ORCID ID that is not listed on this page, please forward this information to us and we will update your Reactome pathway records.

Name Email address

Pathways reviewed by Naim, Hassan Y (189058)

DB_ID Name
5659898 Intestinal saccharidase deficiencies

Details on Person Naim, Hassan Y

Class:IdPerson:189058
_displayNameNaim, Hassan Y
_timestamp2017-08-22 20:38:29
affiliation[Affiliation:5675266] Department of Physiological Chemistry, University of Veterinary Medicine
created[InstanceEdit:189008] D'Eustachio, P, 2006-11-03 14:39:28
firstnameHassan Y
initialHY
modified[InstanceEdit:5659863] D'Eustachio, Peter, 2014-12-23
[InstanceEdit:5675267] D'Eustachio, Peter, 2015-02-15
surnameNaim
(author)[LiteratureReference:189080] Proteolytic processing of human lactase-phlorizin hydrolase is a two-step event: identification of the cleavage sites
[LiteratureReference:195882] Effects of altering palmitylation sites on biosynthesis and function of the influenza virus hemagglutinin
[LiteratureReference:5659866] Structural basis for substrate selectivity in human maltase-glucoamylase and sucrase-isomaltase N-terminal domains
[LiteratureReference:5659881] Molecular basis of aberrant apical protein transport in an intestinal enzyme disorder
[LiteratureReference:5659889] Novel mutations in the human sucrase-isomaltase gene (SI) that cause congenital carbohydrate malabsorption
[LiteratureReference:5659897] 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
[LiteratureReference:5659915] Congenital sucrase-isomaltase deficiency because of an accumulation of the mutant enzyme in the endoplasmic reticulum
[LiteratureReference:5675268] Congenital sucrase-isomaltase deficiency: heterogeneity of inheritance, trafficking, and function of an intestinal enzyme complex
[LiteratureReference:5675269] Congenital sucrase-isomaltase deficiency arising from cleavage and secretion of a mutant form of the enzyme
[LiteratureReference:5675270] Structural hierarchy of regulatory elements in the folding and transport of an intestinal multidomain protein
List all 12 refering instances
[Change default viewing format]