Your browser doesn't support javascript.
loading
Lowe syndrome patient fibroblasts display Ocrl1-specific cell migration defects that cannot be rescued by the homologous Inpp5b phosphatase.
Coon, Brian G; Mukherjee, Debarati; Hanna, Claudia B; Riese, David J; Lowe, Martin; Aguilar, R Claudio.
Affiliation
  • Coon BG; Department of Biological Sciences, Purdue University, West Lafayette, IN 47907, USA.
Hum Mol Genet ; 18(23): 4478-91, 2009 Dec 01.
Article in En | MEDLINE | ID: mdl-19700499
Subject(s)
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Movement / Phosphoric Monoester Hydrolases / Fibroblasts / Oculocerebrorenal Syndrome Limits: Animals / Humans Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2009 Document type: Article Affiliation country: United States Country of publication: United kingdom
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Movement / Phosphoric Monoester Hydrolases / Fibroblasts / Oculocerebrorenal Syndrome Limits: Animals / Humans Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2009 Document type: Article Affiliation country: United States Country of publication: United kingdom