Works by Peltonen, Leena

Results: 202

The impact of newly identified loci on coronary heart disease, stroke and total mortality in the MORGAM prospective cohorts.

Published in:

Genetic Epidemiology, 2009, v. 33, n. 3, p. 237, doi. 10.1002/gepi.20374

By:

Karvanen, Juha;
Silander, Kaisa;
Kee, Frank;
Tiret, Laurence;
Salomaa, Veikko;
Kuulasmaa, Kari;
Wiklund, Per-Gunnar;
Virtamo, Jarmo;
Saarela, Olli;
Perret, Claire;
Perola, Markus;
Peltonen, Leena;
Cambien, Francois;
Erdmann, Jeanette;
Samani, Nilesh J.;
Schunkert, Heribert;
Evans, Alun

Publication type:

Article

Angiotensin-converting enzyme genotypes in the high- and low-risk area for coronary heart disease in Finland.

Published in:

Genetic Epidemiology, 1995, v. 12, n. 4, p. 391, doi. 10.1002/gepi.1370120407

By:

Perola, Markus;
Sajantila, Antti;
Sarti, Cinzia;
Stengård, Jari;
Tamminen, Markku;
Puska, Pekka;
Huttunen, Jussi;
Tuomilehto, Jaakko;
Peltonen, Leena

Publication type:

Article

Aire regulates negative selection of organ-specific T cells.

Published in:

Nature Immunology, 2003, v. 4, n. 4, p. 350, doi. 10.1038/ni906

By:

Liston, Adrian;
Lesage, Sylvie;
Wilson, Judith;
Peltonen, Leena;
Goodnow, Christopher C.

Publication type:

Article

CLN-1 and CLN-5, genes for infantile and variant late infantile neuronal ceroid lipofuscinoses, are expressed in the embryonic human brain.

Published in:

Journal of Comparative Neurology, 2000, v. 426, n. 3, p. 406, doi. 10.1002/1096-9861(20001023)426:3<406::AID-CNE5>3.0.CO;2-5

By:

Heinonen, Outi;
Salonen, Tarja;
Jalanko, Anu;
Peltonen, Leena;
Copp, Andrew

Publication type:

Article

Several cooperating binding sites mediate the interaction of a lysosomal enzyme with phosphotransferase.

Published in:

EMBO Journal, 1997, v. 16, n. 22, p. 6684, doi. 10.1093/emboj/16.22.6684

By:

Tikkanen, Ritva;
Peltola, Minna;
Oinonen, Carita;
Rouvinen, Juha;
Peltonen, Leena

Publication type:

Article

Types I and IV collagenolytic and plasminogen activator activities in preovulatory ovarian follicles.

Published in:

Journal of Cellular Biochemistry, 1987, v. 34, n. 2, p. 101, doi. 10.1002/jcb.240340204

By:

Palotie, Aarno;
Salo, Tuula;
Vihko, Kimmo K.;
Peltonen, Leena;
Rajaniemi, Hannu

Publication type:

Article

Prevalence of dichromate sensitivity.

Published in:

Contact Dermatitis (01051873), 1983, v. 9, n. 3, p. 190, doi. 10.1111/j.1600-0536.1983.tb04356.x

By:

Peltonen, Leena;
Fräki, Jorma

Publication type:

Article

Comparison of A1-test and Finn chamber test.

Published in:

Contact Dermatitis (01051873), 1981, v. 7, n. 4, p. 192, doi. 10.1111/j.1600-0536.1981.tb04041.x

By:

Peltonen, Leena

Publication type:

Article

Nickel sensitivity in the general population.

Published in:

Contact Dermatitis (01051873), 1979, v. 5, n. 1, p. 27, doi. 10.1111/j.1600-0536.1979.tb05531.x

By:

Peltonen, Leena

Publication type:

Article

Dissection of the molecular pathology of aspartylglucosammuria provides the basis for DNA diagnostics and future therapeutic interventions.

Published in:

Scandinavian Journal of Clinical & Laboratory Investigation, 1993, v. 53, n. S213, p. 19, doi. 10.3109/00365519309090670

By:

Ikonen, Elina;
Syvänen, Ann-Christine;
Peltonen, Leena

Publication type:

Article

New Approaches in Nanomedicine for Ischemic Stroke.

Published in:

Pharmaceutics, 2021, v. 13, n. 5, p. 757, doi. 10.3390/pharmaceutics13050757

By:

Correa-Paz, Clara;
da Silva-Candal, Andrés;
Polo, Ester;
Parcq, Jérôme;
Vivien, Denis;
Maysinger, Dusica;
Pelaz, Beatriz;
Campos, Francisco;
Peltonen, Leena

Publication type:

Article

One and Two-Step In Vitro-In Vivo Correlations Based on USP IV Dynamic Dissolution Applied to Four Sodium Montelukast Products.

Published in:

Pharmaceutics, 2021, v. 13, n. 5, p. 690, doi. 10.3390/pharmaceutics13050690

By:

Prieto-Escolar, Mercedes;
Torrado, Juan J.;
Álvarez, Covadonga;
Ruiz-Picazo, Alejandro;
Simón-Vázquez, Marta;
Govantes, Carlos;
Frias, Jesús;
García-Arieta, Alfredo;
Gonzalez-Alvarez, Isabel;
Bermejo, Marival;
Peltonen, Leena

Publication type:

Article

Excipient-Free Pure Drug Nanoparticles Fabricated by Microfluidic Hydrodynamic Focusing.

Published in:

Pharmaceutics, 2021, v. 13, n. 4, p. 529, doi. 10.3390/pharmaceutics13040529

By:

Arzi, Roni Sverdlov;
Kay, Asaf;
Raychman, Yulia;
Sosnik, Alejandro;
Peltonen, Leena

Publication type:

Article

Structural Polymorphism of Sorafenib Tosylate as a Key Factor in Its Solubility Differentiation.

Published in:

Pharmaceutics, 2021, v. 13, n. 3, p. 384, doi. 10.3390/pharmaceutics13030384

By:

Wiergowska, Gabriela;
Stasiłowicz, Anna;
Miklaszewski, Andrzej;
Lewandowska, Kornelia;
Cielecka-Piontek, Judyta;
Peltonen, Leena;
Beom-Jin, Lee

Publication type:

Article

Iron Oxide Nanoparticle Uptake in Mouse Brachiocephalic Artery Atherosclerotic Plaque Quantified by T 2 -Mapping MRI.

Published in:

Pharmaceutics, 2021, v. 13, n. 2, p. 279, doi. 10.3390/pharmaceutics13020279

By:

Moonen, Rik P. M.;
Coolen, Bram F.;
Sluimer, Judith C.;
Daemen, Mat J. A. P.;
Strijkers, Gustav J.;
Peltonen, Leena

Publication type:

Article

Synthesis and Characterization of Nano-Sized 4-Aminosalicylic Acid–Sulfamethazine Cocrystals.

Published in:

Pharmaceutics, 2021, v. 13, n. 2, p. 277, doi. 10.3390/pharmaceutics13020277

By:

Salem, Ala';
Takácsi-Nagy, Anna;
Nagy, Sándor;
Hagymási, Alexandra;
Gősi, Fruzsina;
Vörös-Horváth, Barbara;
Balić, Tomislav;
Pál, Szilárd;
Széchenyi, Aleksandar;
Peltonen, Leena

Publication type:

Article

Production of Itraconazole Nanocrystal-Based Polymeric Film Formulations for Immediate Drug Release.

Published in:

Pharmaceutics, 2020, v. 12, n. 10, p. 960, doi. 10.3390/pharmaceutics12100960

By:

Karagianni, Anna;
Peltonen, Leena

Publication type:

Article

Design Space and QbD Approach for Production of Drug Nanocrystals by Wet Media Milling Techniques.

Published in:

Pharmaceutics, 2018, v. 10, n. 3, p. 104, doi. 10.3390/pharmaceutics10030104

By:

Peltonen, Leena

Publication type:

Article

Stabilizing Agents for Drug Nanocrystals: Effect on Bioavailability.

Published in:

Pharmaceutics, 2016, v. 8, n. 2, p. 16, doi. 10.3390/pharmaceutics8020016

By:

Tuomela, Annika;
Hirvonen, Jouni;
Peltonen, Leena

Publication type:

Article

Population frequency of myotonic dystrophy: higher than expected frequency of myotonic dystrophy type 2 (DM2) mutation in Finland.

Published in:

European Journal of Human Genetics, 2011, v. 19, n. 7, p. 776, doi. 10.1038/ejhg.2011.23

By:

Suominen, Tiina;
Bachinski, Linda L.;
Auvinen, Satu;
Hackman, Peter;
Baggerly, Keith A.,9;
Angelini, Corrado;
Peltonen, Leena;
Krahe, Ralf;
Udd, Bjarne

Publication type:

Article

NordicDB: a Nordic pool and portal for genome-wide control data.

Published in:

European Journal of Human Genetics, 2010, v. 18, n. 12, p. 1322, doi. 10.1038/ejhg.2010.112

By:

Leu, Monica;
Humphreys, Keith;
Surakka, Ida;
Rehnberg, Emil;
Juha Muilu;
Rosenström, Päivi;
Almgren, Peter;
Jääskeläinen, Juha;
Lifton, Richard P.;
Kyvik, Kirsten Ohm;
Kaprio, Jaakko;
Pedersen, Nancy L.;
Palotie, Aarno;
Hall, Per;
Grönberg, Henrik;
Groop, Leif;
Peltonen, Leena;
Palmgren, Juni;
Ripatti, Samuli

Publication type:

Article

MYO9B polymorphisms in multiple sclerosis.

Published in:

European Journal of Human Genetics, 2009, v. 17, n. 6, p. 840, doi. 10.1038/ejhg.2008.251

By:

Kemppinen, Anu;
Suvela, Minna;
Tienari, Pentti J.;
Elovaara, Irina;
Koivisto, Keijo;
Pirttilä, Tuula;
Reunanen, Mauri;
Rautakorpi, Ilkka;
Hillert, Jan;
Lundmark, Frida;
Oturai, Annette;
Ryder, Lars;
Harbo, Hanne F.;
Celius, Elisabeth G.;
Palotie, Aarno;
Daly, Mark;
Peltonen, Leena;
Saarela, Janna

Publication type:

Article

Genome-wide linkage screen for stature and body mass index in 3.032 families: evidence for sex- and population-specific genetic effects.

Published in:

European Journal of Human Genetics, 2009, v. 17, n. 2, p. 258, doi. 10.1038/ejhg.2008.152

By:

Sammalisto, Sampo;
Hiekkalinna, Tero;
Schwander, Karen;
Kardia, Sharon;
Weder, Alan B.;
Rodriguez, Beatriz L.;
Doria, Alessandro;
Kelly, Jennifer A.;
Bruner, Gail R.;
Harley, John B.;
Redline, Susan;
Larkin, Emma K.;
Patel, Sanjay R.;
Ewan, Amy J. H.;
Weber, James L.;
Perola, Markus;
Peltonen, Leena

Publication type:

Article

Genome-wide search for QTLs for apolipoprotein A-I level in elderly Swedish DZ twins: evidence of female-specific locus on 15q11–13.

Published in:

European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1103, doi. 10.1038/ejhg.2008.50

By:

Magnusson, Patrik K. E.;
Boman, Marcus;
de Faire, Ulf;
Perola, Markus;
Peltonen, Leena;
Pedersen, Nancy L.

Publication type:

Article

Evaluation of HapMap data in six populations of European descent.

Published in:

European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1142, doi. 10.1038/ejhg.2008.77

By:

Lundmark, Per E.;
Liljedahl, Ulrika;
Boomsma, Dorret I.;
Mannila, Heikki;
Martin, Nicholas G.;
Palotie, Aarno;
Peltonen, Leena;
Perola, Markus;
Spector, Tim D.;
Syvänen, Ann-Christine

Publication type:

Article

Within-family outliers: segregating alleles or environmental effects? A linkage analysis of height from 5815 sibling pairs.

Published in:

European Journal of Human Genetics, 2008, v. 16, n. 4, p. 516, doi. 10.1038/sj.ejhg.5201992

By:

Benyamin, Beben;
Perola, Markus;
Cornes, Belinda K.;
Madden, Pamela A. F.;
Palotie, Aarno;
Nyholt, Dale R.;
Montgomery, Grant W.;
Peltonen, Leena;
Martin, Nicholas G.;
Visscher, Peter M.

Publication type:

Article

The federated database – a basis for biobank-based post-genome studies, integrating phenome and genome data from 600 000 twin pairs in Europe.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 7, p. 718, doi. 10.1038/sj.ejhg.5201850

By:

Muilu, Juha;
Peltonen, Leena;
Litton, Jan-Eric

Publication type:

Article

Genetic component of identification, intensity and pleasantness of odours: a Finnish family study.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 5, p. 596, doi. 10.1038/sj.ejhg.5201804

By:

Knaapila, Antti;
Keskitalo, Kaisu;
Kallela, Mikko;
Wessman, Maija;
Sammalisto, Sampo;
Hiekkalinna, Tero;
Palotie, Aarno;
Peltonen, Leena;
Tuorila, Hely;
Perola, Markus

Publication type:

Article

Analysis of four neuroligin genes as candidates for autism.

Published in:

European Journal of Human Genetics, 2005, v. 13, n. 12, p. 1285, doi. 10.1038/sj.ejhg.5201474

By:

Ylisaukko-oja, Tero;
Rehnström, Karola;
Auranen, Mari;
Vanhala, Raija;
Alen, Reija;
Kempas, Elli;
Ellonen, Pekka;
Turunen, Joni A.;
Makkonen, Ismo;
Riikonen, Raili;
Nieminen-von Wendt, Taina;
von Wendt, Lennart;
Peltonen, Leena;
Järvelä, Irma

Publication type:

Article

Family-based association study of DYX1C1 variants in autism.

Published in:

European Journal of Human Genetics, 2005, v. 13, n. 1, p. 127, doi. 10.1038/sj.ejhg.5201272

By:

Ylisaukko-oja, Tero;
Peyrard-Janvid, Myriam;
Lindgren, Cecilia M.;
Rehnström, Karola;
Vanhala, Raija;
Peltonen, Leena;
Järvelä, Irma;
Kere, Juha

Publication type:

Article

RHD maternal-fetal genotype incompatibility and schizophrenia: extending the MFG test to include multiple siblings and birth order.

Published in:

European Journal of Human Genetics, 2004, v. 12, n. 3, p. 192, doi. 10.1038/sj.ejhg.5201129

By:

Kraft, Peter;
Palmer, Christina G. S.;
Woodward, Arthur J.;
Turunen, Joni A.;
Minassian, Sonia;
Paunio, Tiina;
Lönnqvist, Jouko;
Peltonen, Leena;
Sinsheimer, Janet S.

Publication type:

Article

Genetic influences contributing to LDL particle size in familial combined hyperlipidaemia.

Published in:

European Journal of Human Genetics, 2002, v. 10, n. 9, p. 547, doi. 10.1038/sj.ejhg.5200844

By:

Vakkilainen, Juha;
Pajukanta, Paivi;
Cantor, Rita M.;
Nuotio, Ilpo O.;
Lahdenpera, Sanni;
Ylitalo, Kati;
Pihlajamaki, Jussi;
Kovanen, Petri T.;
Laakso, Markku;
Viikari, Jorma S.A.;
Peltonen, Leena;
Taskinen, Marja-Riitta

Publication type:

Article

Linkage disequilibrium in isolated populations: Finland and a young sub-population of Kuusamo.

Published in:

European Journal of Human Genetics, 2000, v. 8, n. 8, p. 604, doi. 10.1038/sj.ejhg.5200482

By:

Varilo, Teppo;
Laan, Maris;
Hovatta, Iiris;
Wiebe, Victor;
Terwilliger, Joseph D;
Peltonen, Leena

Publication type:

Article

Testing of human homologues of murine obesity genes as candidate regions in Finnish obese sib pairs.

Published in:

European Journal of Human Genetics, 1999, v. 7, n. 2, p. 117, doi. 10.1038/sj.ejhg.5200256

By:

Öhman, Miina;
Oksanen, Laura;
Kainulainen, Katariina;
Jänne, Olli A;
Kaprio, Jaakko;
Koskenvuo, Markku;
Mustajoki, Pertti;
Kontula, Kimmo;
Peltonen, Leena

Publication type:

Article

Large-scale purification and preliminary X-ray diffraction studies of human aspartylglucosaminidase.

Published in:

Proteins, 1996, v. 24, n. 2, p. 253, doi. 10.1002/(SICI)1097-0134(199602)24:2<253::AID-PROT12>3.0.CO;2-M

By:

Tikkanen, Ritva;
Rouvinen, Juha;
Törrönen, Anneli;
Kalkkinen, Nisse;
Peltonen, Leena

Publication type:

Article

Antenatal diagnosis of hereditary fetal growth retardation with aminoaciduria, cholestasis, iron overload, and lactic acidosis in the newborn infant.

Published in:

2002

By:

Fellman, Vineta;
Visapaa, Ilona;
Vujic, Mihailo;
Wennerholm, Ulla-Britt;
Peltonen, Leena;
Visapää, Ilona

Publication type:

journal article

Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.

Published in:

2011

By:

Mells, George F;
Floyd, James A B;
Morley, Katherine I;
Cordell, Heather J;
Franklin, Christopher S;
Shin, So-Youn;
Heneghan, Michael A;
Neuberger, James M;
Donaldson, Peter T;
Day, Darren B;
Ducker, Samantha J;
Muriithi, Agnes W;
Wheater, Elizabeth F;
Hammond, Christopher J;
Dawwas, Muhammad F;
Jones, David E;
Peltonen, Leena;
Alexander, Graeme J;
Sandford, Richard N;
Anderson, Carl A

Publication type:

Correction Notice

Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.

Published in:

Nature Genetics, 2011, v. 43, n. 4, p. 329, doi. 10.1038/ng.789

By:

Mells, George F.;
Floyd, James A. B.;
Morley, Katherine I.;
Cordell, Heather J.;
Franklin, Christopher S.;
So-Youn Shin;
Heneghan, Michael A.;
Neuberger, James M.;
Donaldson, Peter T.;
Day, Darren B.;
Ducker, Samantha J.;
Muriithi, Agnes W.;
Wheater, Elizabeth F.;
Hammond, Christopher J.;
Dawwas, Muhammad F.;
Jones, David E.;
Peltonen, Leena;
Alexander, Graeme J.;
Sandford, Richard N.;
Anderson, Carl A.

Publication type:

Article

Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis.

Published in:

2010

By:

Booth, David R.;
Heard, Robert N.;
Stewart, Graeme J.;
Cox, Mathew;
Scott, Rodney J.;
Lechner-Scott, Jeannette;
Goris, An;
Dobosi, Rita;
Dubois, Bénédicte;
Saarela, Janna;
Leppä, Virpi;
Peltonen, Leena;
Pirttila, Tuula;
Cournu-Rebeix, Isabelle;
Fontaine, Bertrand;
Bergamaschi, Laura;
D'Alfonso, Sandra;
Leone, Maurizio;
Lorentzen, Åslaug R;
Harbo, Hanne F.

Publication type:

Letter

Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels.

Published in:

Nature Genetics, 2009, v. 41, n. 11, p. 1170, doi. 10.1038/ng.462

By:

Chambers, John C.;
Weihua Zhang;
Yun Li;
Sehmi, Joban;
Wass, Mark N.;
Zabaneh, Delilah;
Hoggart, Clive;
Bayele, Henry;
McCarthy, Mark I.;
Peltonen, Leena;
Freimer, Nelson B.;
Srai, Surjit K.;
Maxwell, Patrick H.;
Sternberg, Michael J. E.;
Ruokonen, Aimo;
Abecasis, Gonçalo;
Jarvelin, Marjo-Riitta;
Scott, James;
Elliott, Paul;
Kooner, Jaspal S.

Publication type:

Article

Association of common variants in NPPA and NPPB with circulating natriuretic peptides and blood pressure.

Published in:

Nature Genetics, 2009, v. 41, n. 3, p. 348, doi. 10.1038/ng.328

By:

Newton-Cheh, Christopher;
Larson, Martin G.;
Vasan, Ramachandran S.;
Levy, Daniel;
Bloch, Kenneth D.;
Surti, Aarti;
Guiducci, Candace;
Kathiresan, Sekar;
Benjamin, Emelia J.;
Struck, Joachim;
Morgenthaler, Nils G.;
Bergmann, Andreas;
Blankenberg, Stefan;
Kee, Frank;
Nilsson, Peter;
Xiaoyan Yin;
Peltonen, Leena;
Vartiainen, Erkki;
Salomaa, Veikko;
Hirschhorn, Joel N.

Publication type:

Article

Mutations in mRNA export mediator GLE1 result in a fetal motoneuron disease.

Published in:

Nature Genetics, 2008, v. 40, n. 2, p. 155, doi. 10.1038/ng.2007.65

By:

Nousiainen, Heidi O.;
Kestilä, Marjo;
Pakkasjärvi, Niklas;
Honkala, Heli;
Kuure, Satu;
Tallila, Jonna;
Vuopala, Katri;
Ignatius, Jaakko;
Herva, Riitta;
Peltonen, Leena

Publication type:

Article

MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome.

Published in:

Nature Genetics, 2006, v. 38, n. 2, p. 155, doi. 10.1038/ng1714

By:

Kyttälä, Mira;
Tallila, Jonna;
Salonen, Riitta;
Kopra, Outi;
Kohlschmidt, Nicolai;
Paavola-Sakki, Paulina;
Peltonen, Leena;
Kestilä, Marjo

Publication type:

Article

A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis.

Published in:

Nature Genetics, 2005, v. 37, n. 10, p. 1108, doi. 10.1038/ng1647

By:

Lincoln, Matthew R.;
Montpetit, Alexandre;
Cader, M. Zameel;
Saarela, Janna;
Dyment, David A.;
Tiislar, Milvi;
Ferretti, Vincent;
Tienari, Pentti J.;
Sadovnick, A. Dessa;
Peltonen, Leena;
Ebers, George C.;
Hudson, Thomas J.

Publication type:

Article

Familial combined hyperlipidemia is associated with upstream transcription factor 1 (USF1).

Published in:

Nature Genetics, 2004, v. 36, n. 4, p. 371, doi. 10.1038/ng1320

By:

Pajukanta, Päivi;
Lilja, Heidi E.;
Sinsheimer, Janet S.;
Cantor, Rita M.;
Gentile, Massimiliano;
Lusis, Aldons J.;
Duan, Xiaoqun Joyce;
Soro-Paavonen, Aino;
Naukkarinen, Jussi;
Saarela, Janna;
Laakso, Markku;
Ehnholm, Christian;
Taskinen, Marja-Riitta;
Peltonen, Leena

Publication type:

Article

Identification of a variant associated with adult-type hypolactasia.

Published in:

Nature Genetics, 2002, v. 30, n. 2, p. 233, doi. 10.1038/ng826

By:

Enattah, Nabil Sabri;
Sahi, Timo;
Savilahti, Erkki;
Terwilliger, Joseph D.;
Peltonen, Leena;
Järvelä, Irma

Publication type:

Article

Loss-of-function mutations in TYROBP (DAP12) result in a presenile dementia with bone cysts.

Published in:

Nature Genetics, 2000, v. 25, n. 3, p. 357, doi. 10.1038/77153

By:

Paloneva, Juha;
Kestilä, Marjo;
Wu, Jun;
Salminen, Antti;
Böhling, Tom;
Ruotsalainen, Vesa;
Hakola, Panu;
Bakker, Alexander B.H.;
Phillips, Joseph H.;
Pekkarinen, Petra;
Lanier, Lewis L.;
Timonen, Tuomo;
Peltonen, Leena

Publication type:

Article

A new gene, encoding an anion transporter, is mutated in sialic acid storage diseases.

Published in:

Nature Genetics, 1999, v. 23, n. 4, p. 462, doi. 10.1038/70585

By:

Verheijen, Frans W.;
Verbeek, Elly;
Aula, Nina;
Beerens, Cecile E.M.T.;
Havelaar, Adrie C.;
Joosse, Marijke;
Peltonen, Leena;
Aula, Pertti;
Galjaard, Hans;
van der Spek, Peter J.;
Mancini, Grazia M.S.

Publication type:

Article

Primer extension on microarrays for typing single-nucleotide polymorphisms and detecting disease-causing mutations.

Published in:

1999

By:

Pastinen, Tomi;
Raitio, Mirja;
Lindroos, Katarina;
Niini, Paavo;
Katila, Pekka;
Peltonen, Leena;
Syvänen, Ann-Christine

Publication type:

Abstract

CLN5, a novel gene encoding a putative transmembrane protein mutated in Finnish variant late infantile neuronal ceroid lipofuscinosis.

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 286, doi. 10.1038/975

By:

Savukoski, Minna;
Klockars, Tuomas;
Holmberg, Ville;
Santavuori, Pirkko;
Lander, Eric S.;
Peltonen, Leena

Publication type:

Article