Rapola J - Search Results

1

Adenovirus-mediated gene transfer results in decreased lysosomal storage in brain and total correction in liver of aspartylglucosaminuria (AGU) mouse.

Peltola M, Kyttälä A, Heinonen O, Rapola J, Paunio T, Revah F, Peltonen L, Jalanko A. Peltola M, et al. Among authors: rapola j. Gene Ther. 1998 Oct;5(10):1314-21. doi: 10.1038/sj.gt.3300740. Gene Ther. 1998. PMID: 9930336

2

Use of nonviral promoters in adenovirus-mediated gene therapy: reduction of lysosomal storage in the aspartylglucosaminuria mouse.

Virta S, Rapola J, Jalanko A, Laine M. Virta S, et al. Among authors: rapola j. J Gene Med. 2006 Jun;8(6):699-706. doi: 10.1002/jgm.892. J Gene Med. 2006. PMID: 16518877

3

Mice with an aspartylglucosaminuria mutation similar to humans replicate the pathophysiology in patients.

Jalanko A, Tenhunen K, McKinney CE, LaMarca ME, Rapola J, Autti T, Joensuu R, Manninen T, Sipilä I, Ikonen S, Riekkinen P Jr, Ginns EI, Peltonen L. Jalanko A, et al. Among authors: rapola j. Hum Mol Genet. 1998 Feb;7(2):265-72. doi: 10.1093/hmg/7.2.265. Hum Mol Genet. 1998. PMID: 9425233

4

Correction of peripheral lysosomal accumulation in mice with aspartylglucosaminuria by bone marrow transplantation.

Laine M, Richter J, Fahlman C, Rapola J, Renlund M, Peltonen L, Karlsson S, Jalanko A. Laine M, et al. Among authors: rapola j. Exp Hematol. 1999 Sep;27(9):1467-74. doi: 10.1016/s0301-472x(99)00075-2. Exp Hematol. 1999. PMID: 10480438 Free article.

5

A mouse model for Finnish variant late infantile neuronal ceroid lipofuscinosis, CLN5, reveals neuropathology associated with early aging.

Kopra O, Vesa J, von Schantz C, Manninen T, Minye H, Fabritius AL, Rapola J, van Diggelen OP, Saarela J, Jalanko A, Peltonen L. Kopra O, et al. Among authors: rapola j. Hum Mol Genet. 2004 Dec 1;13(23):2893-906. doi: 10.1093/hmg/ddh312. Epub 2004 Sep 30. Hum Mol Genet. 2004. PMID: 15459177

6

Bone marrow transplantation in young aspartylglucosaminuria mice: improved clearance of lysosomal storage in brain by using wild type as compared to heterozygote donors.

Laine M, Ahtiainen L, Rapola J, Richter J, Jalanko A. Laine M, et al. Among authors: rapola j. Bone Marrow Transplant. 2004 Dec;34(11):1001-3. doi: 10.1038/sj.bmt.1704665. Bone Marrow Transplant. 2004. PMID: 15489878 No abstract available.

7

The neuronal ceroid lipofuscinoses: unfolding the genetic defect.

Rapola J, Järvelä I, Peltonen L. Rapola J, et al. Pediatr Pathol. 1991 Nov-Dec;11(6):799-806. doi: 10.3109/15513819109065477. Pediatr Pathol. 1991. PMID: 1663617 Review. No abstract available.

8

Mice with Ppt1Deltaex4 mutation replicate the INCL phenotype and show an inflammation-associated loss of interneurons.

Jalanko A, Vesa J, Manninen T, von Schantz C, Minye H, Fabritius AL, Salonen T, Rapola J, Gentile M, Kopra O, Peltonen L. Jalanko A, et al. Among authors: rapola j. Neurobiol Dis. 2005 Feb;18(1):226-41. doi: 10.1016/j.nbd.2004.08.013. Neurobiol Dis. 2005. PMID: 15649713

9

Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis.

Vesa J, Hellsten E, Verkruyse LA, Camp LA, Rapola J, Santavuori P, Hofmann SL, Peltonen L. Vesa J, et al. Among authors: rapola j. Nature. 1995 Aug 17;376(6541):584-7. doi: 10.1038/376584a0. Nature. 1995. PMID: 7637805

10

Bone marrow transplantation in aspartylglucosaminuria--histopathological and MRI study.

Autti T, Rapola J, Santavuori P, Raininko R, Renlund M, Liukkonen E, Lauronen L, Wirtavuori K, Hietala M, Saarinen-Pihkala U. Autti T, et al. Among authors: rapola j. Neuropediatrics. 1999 Dec;30(6):283-8. doi: 10.1055/s-2007-973506. Neuropediatrics. 1999. PMID: 10706021

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