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1.
Centrosomal abnormalities characterize human and rodent cystic cholangiocytes and are associated with Cdc25A overexpression.
Am J Pathol
; 184(1): 110-21, 2014 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-24211536
2.
Pasireotide is more effective than octreotide in reducing hepatorenal cystogenesis in rodents with polycystic kidney and liver diseases.
Hepatology
; 58(1): 409-21, 2013 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-23172758
3.
Inhibition of Cdc25A suppresses hepato-renal cystogenesis in rodent models of polycystic kidney and liver disease.
Gastroenterology
; 142(3): 622-633.e4, 2012 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-22155366
4.
Hepatic cystogenesis is associated with abnormal expression and location of ion transporters and water channels in an animal model of autosomal recessive polycystic kidney disease.
Am J Pathol
; 173(6): 1637-46, 2008 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-18988797
5.
Cholangiocyte primary cilia are chemosensory organelles that detect biliary nucleotides via P2Y12 purinergic receptors.
Am J Physiol Gastrointest Liver Physiol
; 295(4): G725-34, 2008 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-18687752
6.
Cholangiocyte cilia detect changes in luminal fluid flow and transmit them into intracellular Ca2+ and cAMP signaling.
Gastroenterology
; 131(3): 911-20, 2006 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-16952559
7.
Development and characterization of a cholangiocyte cell line from the PCK rat, an animal model of Autosomal Recessive Polycystic Kidney Disease.
Lab Invest
; 86(9): 940-50, 2006 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-16783394
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