Detalhe da pesquisa
1.
Mutations in the histamine N-methyltransferase gene, HNMT, are associated with nonsyndromic autosomal recessive intellectual disability.
Hum Mol Genet
; 24(20): 5697-710, 2015 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26206890
2.
Truncation of the E3 ubiquitin ligase component FBXO31 causes non-syndromic autosomal recessive intellectual disability in a Pakistani family.
Hum Genet
; 133(8): 975-84, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24623383
3.
An acoustically driven microliter flow chamber on a chip (muFCC) for cell-cell and cell-surface interaction studies.
Chemphyschem
; 9(4): 641-5, 2008 Mar 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-18306189
4.
Calcium-sensing receptor abrogates secretagogue- induced increases in intestinal net fluid secretion by enhancing cyclic nucleotide destruction.
Proc Natl Acad Sci U S A
; 103(25): 9390-7, 2006 Jun 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-16760252
5.
Insulin receptor (IR) and glucose transporter 2 (GLUT2) proteins form a complex on the rat hepatocyte membrane.
Cell Physiol Biochem
; 15(1-4): 51-8, 2005.
Artigo
em Inglês
| MEDLINE | ID: mdl-15665515