Literature DB >> 12420720

Exclusion of the Nurr1 gene in autosomal recessive Parkinson's disease.

Nina Rawal, Magali Periquet, Alexandra Dürr, Giuseppe de Michele, Vincenzo Bonifati, Helio A Teive, Salmo Raskin, Joao Guimaraes, Yves Agid, Alexis Brice.   

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Year:  2002        PMID： 12420720     DOI： 10.1007/s00415-002-0757-6

Source DB:  PubMed          Journal:  J Neurol        ISSN： 0340-5354            Impact factor:   4.849


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  15 in total

1.  Early developmental destruction of terminals in the striatal target induces apoptosis in dopamine neurons of the substantia nigra.

Authors:  M J Marti; C J James; T F Oo; W J Kelly; R E Burke
Journal:  J Neurosci       Date:  1997-03-15       Impact factor: 6.167

2.  A selective group of dopaminergic neurons express Nurr1 in the adult mouse brain.

Authors:  C Bäckman; T Perlmann; A Wallén; B J Hoffer; M Morales
Journal:  Brain Res       Date:  1999-12-18       Impact factor: 3.252

3.  Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism.

Authors:  T Kitada; S Asakawa; N Hattori; H Matsumine; Y Yamamura; S Minoshima; M Yokochi; Y Mizuno; N Shimizu
Journal:  Nature       Date:  1998-04-09       Impact factor: 49.962

4.  Nurr1 enhances transcription of the human dopamine transporter gene through a novel mechanism.

Authors:  P Sacchetti; T R Mitchell; J G Granneman; M J Bannon
Journal:  J Neurochem       Date:  2001-03       Impact factor: 5.372

5.  Developmental cell death in dopaminergic neurons of the substantia nigra of mice.

Authors:  V Jackson-Lewis; M Vila; R Djaldetti; C Guegan; G Liberatore; J Liu; K L O'Malley; R E Burke; S Przedborski
Journal:  J Comp Neurol       Date:  2000-08-28       Impact factor: 3.215

6.  Faster sequential genetic linkage computations.

Authors:  R W Cottingham; R M Idury; A A Schäffer
Journal:  Am J Hum Genet       Date:  1993-07       Impact factor: 11.025

7.  A second independent pathway for development of mesencephalic dopaminergic neurons requires Lmx1b.

Authors:  M P Smidt; C H Asbreuk; J J Cox; H Chen; R L Johnson; J P Burbach
Journal:  Nat Neurosci       Date:  2000-04       Impact factor: 24.884

8.  A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.

Authors:  N Abbas; C B Lücking; S Ricard; A Dürr; V Bonifati; G De Michele; S Bouley; J R Vaughan; T Gasser; R Marconi; E Broussolle; C Brefel-Courbon; B S Harhangi; B A Oostra; E Fabrizio; G A Böhme; L Pradier; N W Wood; A Filla; G Meco; P Denefle; Y Agid; A Brice
Journal:  Hum Mol Genet       Date:  1999-04       Impact factor: 6.150

9.  NURR1 mutations in cases of schizophrenia and manic-depressive disorder.

Authors:  S Buervenich; A Carmine; M Arvidsson; F Xiang; Z Zhang; O Sydow; E G Jönsson; G C Sedvall; S Leonard; R G Ross; R Freedman; K V Chowdari; V L Nimgaonkar; T Perlmann; M Anvret; L Olson
Journal:  Am J Med Genet       Date:  2000-12-04

10.  Dopamine neuron agenesis in Nurr1-deficient mice.

Authors:  R H Zetterström; L Solomin; L Jansson; B J Hoffer; L Olson; T Perlmann
Journal:  Science       Date:  1997-04-11       Impact factor: 47.728
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  1 in total

Review 1.  Pathological proteins in Parkinson's disease: focus on the proteasome.

Authors:  Heather Snyder; Benjamin Wolozin
Journal:  J Mol Neurosci       Date:  2004       Impact factor: 3.444
  1 in total

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