Con inversi�n constante

May 2008
Vistazo;Empresas Supplement, p22
No abstract available.


Related Articles

  • Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouse. Morgan, David // Nature Genetics;Nov98, Vol. 20 Issue 3, p312 

    Presents a correct reprint to an article about inversin gene deletion in mouse.

  • In the Clear. Mooney, Loren // Sports Illustrated;12/28/98-1/4/99, Vol. 89 Issue 26, Following p38 

    Evaluates the Smith Turbo Constant Air Management goggles for skiing. Cost; Key features; Pros and cons.

  • BOOK REVIEWS. Fry, W. // Pacific Affairs;Spring2001, Vol. 74 Issue 1, p132 

    Reviews the book `Mother's Beloved: Stories From Laos,' by Outhine Bounyavong, edited by Bounheng Inversin and Daniel Duffy, introduction by Peter Koret.

  • Inversine for Tourette syndrome symptoms.  // Latitudes;2002, Vol. 5 Issue 3, p6 

    Studies the use of inversine for treating Tourette syndrome symptoms. Data indicating that the drug may have reduced sudden mood changes but it was not an effective treatment for tics or the total spectrum of symptoms associated with Tourette's syndrome.

  • TRIAD.  // Business North Carolina;Nov2002, Vol. 22 Issue 11, p18 

    Presents updates on several companies in North Carolina as of November 2002. Closure of facilities owned by Burlington Industries; Buyback of the shares of 1st State Bancorp; Acquisition of the hypertension drug Inversine by Targacept from Layton Bioscience.

  • Linking cilia to Wnts. Germino, Gregory G. // Nature Genetics;May2005, Vol. 37 Issue 5, p455 

    Inversin is a component of a poorly understood cilia-based mechanism responsible for specifying the left-right axis during development and for maintaining normal kidney architecture throughout life. A new study now suggests that inversin might act as a flow-regulated molecular switch between...

  • Inversin, the gene product mutated in nephronophthisis type II, functions as a molecular switch between Wnt signaling pathways. Simons, Matias; Gloy, Joachim; Ganner, Athina; Bullerkotte, Axel; Bashkurov, Mikhail; Krönig, Corinna; Schermer, Bernhard; Benzing, Thomas; Cabello, Olga A; Jenny, Andreas; Mlodzik, Marek; Polok, Bozena; Driever, Wolfgang; Obara, Tomoko; Walz, Gerd // Nature Genetics;May2005, Vol. 37 Issue 5, p537 

    Cystic renal diseases are caused by mutations of proteins that share a unique subcellular localization: the primary cilium of tubular epithelial cells. Mutations of the ciliary protein inversin cause nephronophthisis type II, an autosomal recessive cystic kidney disease characterized by...

  • CRITICS' CHOICE.  // Daily Mail;2/26/2013, p44 


  • Con-way Yields Tonnage.  // Traffic World;10/23/2006, Vol. 270 Issue 43, p24 

    The article reports on the decrease in the third-quarter profits for LTL giant Con-way Freight Inc. and parent company Con-Way Inc. in the U.S. The decrease in the corporate profits is due to an anticipated drop in tonnage drove. According to Douglas W. Stotlar, president and CEO of Con-way,...

  • Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination. Otto, Edgar A.; Schermer, Bernhard; Obara, Tomoko; O'Toole, John F.; Hiller, Karl S.; Mueller, Adelheid M.; Ruf, Rainer G.; Hoefele, Julia; Beekmann, Frank; Landau, Daniel; Foreman, John W.; Goodship, Judith A.; Strachan, Tom; Kispert, Andreas; Wolf, Matthias T.; Gagnadoux, Marie F.; Nivet, Hubert; Antignac, Corine; Walz, Gerd // Nature Genetics;Aug2003, Vol. 34 Issue 4, p413 

    Nephronophthisis (NPHP), an autosomal recessive cystic kidney disease, leads to chronic renal failure in children. The genes mutated in NPHP1 and NPHP4 have been identified, and a gene locus associated with infantile nephronophthisis (NPHP2) was mapped. The kidney phenotype of NPHP2 combines...


Read the Article


Sorry, but this item is not currently available from your library.

Try another library?
Sign out of this library

Other Topics