Jalanko A - Search Results

1

Biosynthesis and intracellular targeting of the CLN3 protein defective in Batten disease.

Järvelä I, Sainio M, Rantamäki T, Olkkonen VM, Carpén O, Peltonen L, Jalanko A. Järvelä I, et al. Among authors: jalanko a. Hum Mol Genet. 1998 Jan;7(1):85-90. doi: 10.1093/hmg/7.1.85. Hum Mol Genet. 1998. PMID: 9384607

2

Lysosomal localization of the neuronal ceroid lipofuscinosis CLN5 protein.

Isosomppi J, Vesa J, Jalanko A, Peltonen L. Isosomppi J, et al. Among authors: jalanko a. Hum Mol Genet. 2002 Apr 15;11(8):885-91. doi: 10.1093/hmg/11.8.885. Hum Mol Genet. 2002. PMID: 11971870

3

Interconnections of CLN3, Hook1 and Rab proteins link Batten disease to defects in the endocytic pathway.

Luiro K, Yliannala K, Ahtiainen L, Maunu H, Järvelä I, Kyttälä A, Jalanko A. Luiro K, et al. Among authors: jalanko a. Hum Mol Genet. 2004 Dec 1;13(23):3017-27. doi: 10.1093/hmg/ddh321. Epub 2004 Oct 7. Hum Mol Genet. 2004. PMID: 15471887

4

Defective intracellular transport of CLN3 is the molecular basis of Batten disease (JNCL).

Järvelä I, Lehtovirta M, Tikkanen R, Kyttälä A, Jalanko A. Järvelä I, et al. Among authors: jalanko a. Hum Mol Genet. 1999 Jun;8(6):1091-8. doi: 10.1093/hmg/8.6.1091. Hum Mol Genet. 1999. PMID: 10332042

5

Detection of eight novel palmitoyl protein thioesterase (PPT) mutations underlying infantile neuronal ceroid lipofuscinosis (INCL;CLN1).

Salonen T, Järvelä I, Peltonen L, Jalanko A. Salonen T, et al. Among authors: jalanko a. Hum Mutat. 2000;15(3):273-9. doi: 10.1002/(SICI)1098-1004(200003)15:3<273::AID-HUMU8>3.0.CO;2-L. Hum Mutat. 2000. PMID: 10679943

6

Human palmitoyl protein thioesterase: evidence for lysosomal targeting of the enzyme and disturbed cellular routing in infantile neuronal ceroid lipofuscinosis.

Hellsten E, Vesa J, Olkkonen VM, Jalanko A, Peltonen L. Hellsten E, et al. Among authors: jalanko a. EMBO J. 1996 Oct 1;15(19):5240-5. EMBO J. 1996. PMID: 8895569 Free PMC article.

7

Neuronal ceroid lipofuscinoses are connected at molecular level: interaction of CLN5 protein with CLN2 and CLN3.

Vesa J, Chin MH, Oelgeschläger K, Isosomppi J, DellAngelica EC, Jalanko A, Peltonen L. Vesa J, et al. Among authors: jalanko a. Mol Biol Cell. 2002 Jul;13(7):2410-20. doi: 10.1091/mbc.e02-01-0031. Mol Biol Cell. 2002. PMID: 12134079 Free PMC article.

8

Unraveling the molecular pathogenesis of free sialic acid storage disorders: altered targeting of mutant sialin.

Aula N, Jalanko A, Aula P, Peltonen L. Aula N, et al. Among authors: jalanko a. Mol Genet Metab. 2002 Sep-Oct;77(1-2):99-107. doi: 10.1016/s1096-7192(02)00124-5. Mol Genet Metab. 2002. PMID: 12359136

9

A novel aspartylglucosaminuria mutation affects translocation of aspartylglucosaminidase.

Saarela J, von Schantz C, Peltonen L, Jalanko A. Saarela J, et al. Among authors: jalanko a. Hum Mutat. 2004 Oct;24(4):350-1. doi: 10.1002/humu.9276. Hum Mutat. 2004. PMID: 15365992

10

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: jalanko a. 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

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