Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Rodolfo S. Martin"'
Autor:
Hartmut P. H. Neumann, Carolina Muchnik, Paula Virginia Iscoff, Maria Florencia Martinez, Adriana Fraga, Pablo Javier Azurmendi, Elisabet M. Oddo, Luis Daniel Mazzuoccolo, Rodolfo S. Martin
Publikováno v:
Nephron. 140(4)
The calcium signalling and hedgehog (HH) signalling pathways operate in the primary cilium. Abnormalities in these pathways cause autosomal dominant polycystic kidney disease (ADPKD) and naevoid basal cell carcinoma syndrome (NBCCS) respectively. Sev
Autor:
Elisabeth M. Oddo, Elvira Arrizurieta, Rodolfo S. Martin, Fernando R. Ibarra, Rafael Krmar, Verónica De Luca Sarobe
Publikováno v:
Nephron Physiology. 108:p37-p45
Aims: To test whether blood pressure is affected by potassium supplementation which modifies urinary kallikrein (UK) in SHR of either sex, and to elucidate the mechanisms involved. Design: In SHR and WKY blood pressure, renal function and hormonal pr
Autor:
Gabriela A. Periz, Fernando R. Ibarra, Rodolfo S. Martin, Elvira Arrizurieta, Elisabet M. Oddo, Rafael Krmar, Horacio Herrera, Verónica De Luca Sarobe
Publikováno v:
Clinical and Experimental Hypertension. 28:157-170
It has been suggested that an abnormal activity of the hypothalamic-pituitary-adrenal-gonadal axis may be implicated in the pathogenesis of spontaneously hypertensive rats (SHR) blood pressure hypertension. However, it is widely known that the kallik
Autor:
Jorge E. Toledo, Elvira Arrizurieta, Rodolfo S. Martin, Fernando R. Ibarra, Claudia A. Bertuccio
Publikováno v:
American Journal of Physiology-Renal Physiology. 282:F265-F270
Previous reports have shown a stimulatory effect of vasopressin (VP) on Na-K-ATPase and rBSC-1 expression and activity. Whether these VP-dependent mechanisms are operating in vivo in physiological conditions as well as in chronic renal failure (CRF)
Autor:
Diana M. Iglesias, Bernard F. King, Yves Pirson, Vicente E. Torres, Patrick S. Kamath, John Huston, Cathy T. Falk, Rodolfo S. Martin, Clarence Shub, Airong Li, David Reynolds, Stefan Somlo
Publikováno v:
The American Journal of Human Genetics. 67(6):1598-1604
Polycystic liver disease (PCLD) is characterized by the growth of fluid-filled cysts of biliary epithelial origin in the liver. Although the disease is often asymptomatic, it can, when severe, lead to complications requiring surgical therapy. PCLD is
Autor:
Mariana Herrera, Diana M. Iglesias, Juan A. Palmitano, Elvira Arrizurieta, Alberto R. Kornblihtt, Viviana Bernath, Rodolfo S. Martin
Publikováno v:
Digestive Diseases and Sciences. 44:385-388
Autosomal dominant polycystic liver disease occurs commonly in association with autosomal dominant polycystic kidney disease, types 1 and 2. It may also exist as a separate entity, genetically distinct from autosomal dominant polycystic kidney diseas
Autor:
Nadine Ortiz Bruechle, Peter Dr. Riegler, Elke Schaeffner, Christian Burchardi, Janina Bacher, Pablo Javier Azurmendi, Michael Hoffmann, Hartmut P. H. Neumann, Zinaida Nabulsi, Angelica Malinoc, Sven Gläsker, Annette Kraemer-Guth, Vera Ivanovas, Charis Eng, Rodolfo S. Martin, Klaus Zerres, Irina Mader, Cordula A. Jilg
Publikováno v:
Cerebrovascular diseases / Extra 2(1), 71-79 (2012). doi:10.1159/000342620
Cerebrovascular Diseases Extra, Vol 2, Iss 1, Pp 71-79 (2012)
Cerebrovascular Diseases Extra
Cerebrovascular Diseases Extra, Vol 2, Iss 1, Pp 71-79 (2012)
Cerebrovascular Diseases Extra
Cerebrovascular diseases / Extra 2(1), 71-79 (2012). doi:10.1159/000342620
Published by Karger, Basel
Published by Karger, Basel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93b1543900c9e902038d779bb10fde07
Autor:
Felicita M. Galan, Adriana Fraga, Elvira Arrizurieta, Jose S. Santelha Stefan, Pedro Forcada, Marta G. Valdez, Rodolfo S. Martin, Carol Kotliar, Pablo Javier Azurmendi
Publikováno v:
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association. 24(8)
Autosomal dominant polycystic kidney disease (ADPKD) shows an increase in both urine monocyte chemoattractant protein-1 (MCP-1) and carotid intima-media thickness (CIMT) before changes in serum creatinine concentration. Although microalbuminuria is a
Autor:
Pia Tahvanainen, Airong Li, Richard P. Lifton, Patrick S. Kamath, Yves Pirson, Stefan Somlo, Yiqiang Cai, Helena Kääriäinen, Bernard F. King, Vicente E. Torres, Xin Tian, Laszlo Furu, Ali G. Gharavi, Krister Höckerstedt, Sonia Davila, Rodolfo S. Martin, Qi Qian, Tamehito Onoe, Pablo Javier Azurmendi, Olivier Devuyst, Esa Tahvanainen
Publikováno v:
Nature genetics. 36(6)
Mutations in PRKCSH, encoding the beta-subunit of glucosidase II, an N-linked glycan-processing enzyme in the endoplasmic reticulum (ER), cause autosomal dominant polycystic liver disease. We found that mutations in SEC63, encoding a component of the
Autor:
Rodolfo S. Martin, Elvira Arrizurieta, Fernando R. Ibarra, Claudia A. Bertuccio, Sam X. Cheng
Publikováno v:
Pflugers Archiv : European journal of physiology. 447(1)
Sodium transport correlates with varying Na+-K+-ATPase activity rates along the nephron. Whether differences in Na+-K+-ATPase regulation by protein kinase C-dependent phosphorylation are also present has not been tested. We measured the degree of Na+