Peltonen L

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References (13)

Title : Analysis of four neuroligin genes as candidates for autism - Ylisaukko-oja_2005_Eur.J.Hum.Genet_13_1285
Author(s) : Ylisaukko-oja T , Rehnstrom K , Auranen M , Vanhala R , Alen R , Kempas E , Ellonen P , Turunen JA , Makkonen I , Riikonen R , Nieminen-von Wendt T , von Wendt L , Peltonen L , Jarvela I
Ref : Eur J Hum Genet , 13 :1285 , 2005
Abstract : Ylisaukko-oja_2005_Eur.J.Hum.Genet_13_1285
ESTHER : Ylisaukko-oja_2005_Eur.J.Hum.Genet_13_1285
PubMedSearch : Ylisaukko-oja_2005_Eur.J.Hum.Genet_13_1285
PubMedID: 16077734
Gene_locus related to this paper: human-NLGN4Y , human-NLGN1 , human-NLGN3 , human-NLGN4X

Title : Mice with Ppt1Deltaex4 mutation replicate the INCL phenotype and show an inflammation-associated loss of interneurons - Jalanko_2005_Neurobiol.Dis_18_226
Author(s) : Jalanko A , Vesa J , Manninen T , von Schantz C , Minye H , Fabritius AL , Salonen T , Rapola J , Gentile M , Kopra O , Peltonen L
Ref : Neurobiol Dis , 18 :226 , 2005
Abstract : Jalanko_2005_Neurobiol.Dis_18_226
ESTHER : Jalanko_2005_Neurobiol.Dis_18_226
PubMedSearch : Jalanko_2005_Neurobiol.Dis_18_226
PubMedID: 15649713
Gene_locus related to this paper: mouse-ppt

Title : Detection of eight novel palmitoyl protein thioesterase (PPT) mutations underlying infantile neuronal ceroid lipofuscinosis (INCL\;CLN1) - Salonen_2000_Hum.Mutat_15_273
Author(s) : Salonen T , Jarvela I , Peltonen L , Jalanko A
Ref : Hum Mutat , 15 :273 , 2000
Abstract : Salonen_2000_Hum.Mutat_15_273
ESTHER : Salonen_2000_Hum.Mutat_15_273
PubMedSearch : Salonen_2000_Hum.Mutat_15_273
PubMedID: 10679943
Gene_locus related to this paper: human-PPT1

Title : Expression of palmitoyl protein thioesterase in neurons. -
Author(s) : Heinonen O , Kyttala A , Lehmus E , Paunio T , Peltonen L , Jalanko A
Ref : Molec Genet Metab , 69 :123 , 2000
PubMedID:
Gene_locus related to this paper: human-PPT1

Title : Expression of palmitoyl protein thioesterase in neurons - Heinonen_2000_Mol.Genet.Metab_69_123
Author(s) : Heinonen O , Kyttala A , Lehmus E , Paunio T , Peltonen L , Jalanko A
Ref : Mol Genet Metab , 69 :123 , 2000
Abstract : Heinonen_2000_Mol.Genet.Metab_69_123
ESTHER : Heinonen_2000_Mol.Genet.Metab_69_123
PubMedSearch : Heinonen_2000_Mol.Genet.Metab_69_123
PubMedID: 10720439

Title : Mouse palmitoyl protein thioesterase: gene structure and expression of cDNA - Salonen_1998_Genome.Res_8_724
Author(s) : Salonen T , Hellsten E , Horelli-Kuitunen N , Peltonen L , Jalanko A
Ref : Genome Res , 8 :724 , 1998
Abstract : Salonen_1998_Genome.Res_8_724
ESTHER : Salonen_1998_Genome.Res_8_724
PubMedSearch : Salonen_1998_Genome.Res_8_724
PubMedID: 9685319
Gene_locus related to this paper: mouse-ppt

Title : Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis - Vesa_1995_Nature_376_584
Author(s) : Vesa J , Hellsten E , Verkruyse LA , Camp LA , Rapola J , Santavuori P , Hofmann SL , Peltonen L
Ref : Nature , 376 :584 , 1995
Abstract : Vesa_1995_Nature_376_584
ESTHER : Vesa_1995_Nature_376_584
PubMedSearch : Vesa_1995_Nature_376_584
PubMedID: 7637805
Gene_locus related to this paper: human-PPT1

Title : Identification of YAC clones for human chromosome 1p32 and physical mapping of the infantile neuronal ceroid lipofuscinosis (INCL) locus - Hellsten_1995_Genomics_25_404
Author(s) : Hellsten E , Vesa J , Heiskanen M , Makela TP , Jarvela I , Cowell JK , Mead S , Alitalo K , Palotie A , Peltonen L
Ref : Genomics , 25 :404 , 1995
Abstract : Hellsten_1995_Genomics_25_404
ESTHER : Hellsten_1995_Genomics_25_404
PubMedSearch : Hellsten_1995_Genomics_25_404
PubMedID: 7789974
Gene_locus related to this paper: human-PPT1

Title : Identification of a novel mutation causing aspartylglucosaminuria reveals a mutation hotspot region in the aspartylglucosaminidase gene - Isoniemi_1995_Hum.Mutat_5_318
Author(s) : Isoniemi A , Hietala M , Aula P , Jalanko A , Peltonen L
Ref : Hum Mutat , 5 :318 , 1995
Abstract : Isoniemi_1995_Hum.Mutat_5_318
ESTHER : Isoniemi_1995_Hum.Mutat_5_318
PubMedSearch : Isoniemi_1995_Hum.Mutat_5_318
PubMedID: 7627186

Title : Refined assignment of the infantile neuronal ceroid lipofuscinosis (INCL, CLN1) locus at 1p32: incorporation of linkage disequilibrium in multipoint analysis - Hellsten_1993_Genomics_16_720
Author(s) : Hellsten E , Vesa J , Speer MC , Makela TP , Jarvela I , Alitalo K , Ott J , Peltonen L
Ref : Genomics , 16 :720 , 1993
Abstract : Hellsten_1993_Genomics_16_720
ESTHER : Hellsten_1993_Genomics_16_720
PubMedSearch : Hellsten_1993_Genomics_16_720
PubMedID: 8325646
Gene_locus related to this paper: human-PPT1

Title : Assignment of the infantile form of neuronal ceroid lipofuscinosis (INCL, CLN1) to the short arm of chromosome 1 (Abstract) -
Author(s) : Jarvela I , Santavuori P , Vesa J , Rapola J , Palotie A , Peltonen L
Ref : Cytogenet Cell Genet , 58 :1856 , 1991
PubMedID:
Gene_locus related to this paper: human-PPT1

Title : Infantile neuronal ceroid-lipofuscinosis is not an allelic form of Batten disease: exclusion of chromosome 16 region with linkage analyses - Jokiaho_1990_Genomics_8_391
Author(s) : Jokiaho I , Puhakka L , Santavuori P , Manninen T , Nyman K , Peltonen L
Ref : Genomics , 8 :391 , 1990
Abstract : Jokiaho_1990_Genomics_8_391
ESTHER : Jokiaho_1990_Genomics_8_391
PubMedSearch : Jokiaho_1990_Genomics_8_391
PubMedID: 2249855
Gene_locus related to this paper: human-PPT1