Works matching IS 13646745 AND DT 2006 AND VI 7 AND IP 3

Results: 8

Founder effect for the Ala431Glu mutation of the presenilin 1 gene causing early-onset Alzheimer’s disease in Mexican families.
Published in:
Neurogenetics, 2006, v. 7, n. 3, p. 195, doi. 10.1007/s10048-006-0043-3
By:
- Yescas, Petra;
- Huertas-Vazquez, Adriana;
- Villarreal-Molina, María;
- Rasmussen, Astrid;
- Tusié-Luna, María Teresa;
- López, Marisol;
- Canizales-Quinteros, Samuel;
- Alonso, María Elisa
Publication type:
Article
A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson’s disease risk in Taiwan.
Published in:
Neurogenetics, 2006, v. 7, n. 3, p. 133, doi. 10.1007/s10048-006-0041-5
By:
- Di Fonzo, Alessio;
- Yah-Huei Wu-Chou;
- Chin-Song Lu;
- van Doeselaar, Marina;
- Simons, Erik J.;
- Rohé, Christan F.;
- Hsiu-Chen Chang;
- Rou-Shayn Chen;
- Yi-Hsin Weng;
- Vanacore, Nicola;
- Breedveld, Guido J.;
- Oostra, Ben A.;
- Bonifati, Vincenzo
Publication type:
Article
Transcriptome analysis reveals link between proteasomal and mitochondrial pathways in Parkinson’s disease.
Published in:
Neurogenetics, 2006, v. 7, n. 3, p. 139, doi. 10.1007/s10048-006-0033-5
By:
- Duke, D. C.;
- Moran, L. B.;
- Kalaitzakis, M. E.;
- Deprez, M.;
- Dexter, D. T.;
- Pearce, R. K. B.;
- Graeber, M. B.
Publication type:
Article
Spastic paraplegia with thin corpus callosum: description of 20 new families, refinement of the SPG11 locus, candidate gene analysis and evidence of genetic heterogeneity.
Published in:
Neurogenetics, 2006, v. 7, n. 3, p. 149, doi. 10.1007/s10048-006-0044-2
By:
- Stevanin, Giovanni;
- Montagna, Giorgia;
- Azzedine, Hamid;
- Valente, Enza Maria;
- Durr, Alexandra;
- Scarano, Valentina;
- Bouslam, Naima;
- Cassandrini, Denise;
- Denora, Paola S.;
- Criscuolo, Chiara;
- Belarbi, Soraya;
- Orlacchio, Antonio;
- Jonveaux, Philippe;
- Silvestri, Gabriella;
- Ouvard Hernandez, Anne Marie;
- De Michele, Giuseppe;
- Tazir, Meriem;
- Mariotti, Caterina;
- Brockmann, Knut;
- Malandrini, Alessandro
Publication type:
Article
Investigation of autism and GABA receptor subunit genes in multiple ethnic groups.
Published in:
Neurogenetics, 2006, v. 7, n. 3, p. 167, doi. 10.1007/s10048-006-0045-1
By:
- Collins, Ann L.;
- Deqiong Ma;
- Whitehead, Patrice L.;
- Martin, Eden R.;
- Wright, Harry H.;
- Abramson, Ruth K.;
- Hussman, John P.;
- Haines, Jonathan L.;
- Cuccaro, Michael L.;
- Gilbert, John R.;
- Pericak-Vance, Margaret A.
Publication type:
Article
Parsing the genetic heterogeneity of chromosome 12q susceptibility genes for Alzheimer disease by family-based association analysis.
Published in:
Neurogenetics, 2006, v. 7, n. 3, p. 157, doi. 10.1007/s10048-006-0047-z
By:
- Ping-I Lin;
- Martin, Eden R.;
- Browning-Large, Carrie A.;
- Schmechel, Donald E.;
- Welsh-Bohmer, Kathleen A.;
- Murali Doraiswamy, P.;
- Gilbert, John R.;
- Haines, Jonathan L.;
- Pericak-Vance, Margaret A.
Publication type:
Article
Molecular mechanism of rigid spine with muscular dystrophy type 1 caused by novel mutations of selenoprotein N gene.
Published in:
Neurogenetics, 2006, v. 7, n. 3, p. 175, doi. 10.1007/s10048-006-0046-0
By:
- Okamoto, Yuji;
- Takashima, Hiroshi;
- Higuchi, Itsuro;
- Matsuyama, Wataru;
- Suehara, Masahito;
- Nishihira, Yasushi;
- Hashiguchi, Akihiro;
- Hirano, Ryuki;
- Ng, Arlene;
- Nakagawa, Masanori;
- Izumo, Shuji;
- Osame, Mitsuhiro;
- Arimura, Kimiyoshi
Publication type:
Article
Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL.
Published in:
Neurogenetics, 2006, v. 7, n. 3, p. 185, doi. 10.1007/s10048-006-0049-x
By:
- Annunen-Rasila, Johanna;
- Finnilä, Saara;
- Mykkänen, Kati;
- Moilanen, Jukka S.;
- Veijola, Johanna;
- Pöyhönen, Minna;
- Viitanen, Matti;
- Kalimo, Hannu;
- Majamaa, Kari
Publication type:
Article