Literature DB >> 9545499

A high-resolution genetic map of mouse chromosome 19 encompassing the muscle-deficient osteochondrodystrophy (mdf-ocd) region.

C Poirier1, S Blot, M Fernandes, G F Carle, V Stanescu, R Stanescu, J L Guénet.   

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Year:  1998        PMID： 9545499     DOI： 10.1007/s003359900777

Source DB:  PubMed          Journal:  Mamm Genome        ISSN： 0938-8990            Impact factor:   2.957


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  13 in total

1.  Ciliary neurotrophic factor prevents degeneration of motor neurons in mouse mutant progressive motor neuronopathy.

Authors:  M Sendtner; H Schmalbruch; K A Stöckli; P Carroll; G W Kreutzberg; H Thoenen
Journal:  Nature       Date:  1992-08-06       Impact factor: 49.962

2.  The mouse homologs of RELA and MLK3 are located within a 120-kb fragment on chromosome 19.

Authors:  M Fernandes; C Poirier; N J Lassam; C Larsson; J Guénet; P Gaudray; G F Carle
Journal:  Mamm Genome       Date:  1997-07       Impact factor: 2.957

3.  Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms.

Authors:  M Orita; H Iwahana; H Kanazawa; K Hayashi; T Sekiya
Journal:  Proc Natl Acad Sci U S A       Date:  1989-04       Impact factor: 11.205

4.  Structure and chromosomal assignment of the mouse fra-1 gene, and its exclusion as a candidate gene for oc (osteosclerosis).

Authors:  M Schreiber; C Poirier; A Franchi; R Kurzbauer; J L Guenet; G F Carle; E F Wagner
Journal:  Oncogene       Date:  1997-09-04       Impact factor: 9.867

5.  Chromosomal localization of genes encoding the transcription factors, c-rel, NF-kappa Bp50, NF-kappa Bp65, and lyt-10 by fluorescence in situ hybridization.

Authors:  S Mathew; V V Murty; R Dalla-Favera; R S Chaganti
Journal:  Oncogene       Date:  1993-01       Impact factor: 9.867

6.  A genetic map of the mouse with 4,006 simple sequence length polymorphisms.

Authors:  W F Dietrich; J C Miller; R G Steen; M Merchant; D Damron; R Nahf; A Gross; D C Joyce; M Wessel; R D Dredge
Journal:  Nat Genet       Date:  1994-06       Impact factor: 38.330

7.  Assignment of the human FAU gene to a subregion of chromosome 11q13.

Authors:  K Kas; E Schoenmakers; W van de Ven; G Weber; M Nordenskjöld; L Michiels; J Merregaert; C Larsson
Journal:  Genomics       Date:  1993-08       Impact factor: 5.736

8.  Reverse mapping of the gene encoding the human fos-related antigen-1 (fra-1) within chromosome band 11q13.

Authors:  R J Sinke; A Tanigami; Y Nakamura; A Geurts van Kessel
Journal:  Genomics       Date:  1993-10       Impact factor: 5.736

9.  Chromosomal localization of the human ciliary neurotrophic factor gene (CNTF) to 11q12 by fluorescence in situ hybridization.

Authors:  M Giovannini; A J Romo; G A Evans
Journal:  Cytogenet Cell Genet       Date:  1993

10.  MAPMAKER: an interactive computer package for constructing primary genetic linkage maps of experimental and natural populations.

Authors:  E S Lander; P Green; J Abrahamson; A Barlow; M J Daly; S E Lincoln; L A Newberg; L Newburg
Journal:  Genomics       Date:  1987-10       Impact factor: 5.736
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  6 in total

1.  Gene content and function of the ancestral chromosome fusion site in human chromosome 2q13-2q14.1 and paralogous regions.

Authors:  Yuxin Fan; Tera Newman; Elena Linardopoulou; Barbara J Trask
Journal:  Genome Res       Date:  2002-11       Impact factor: 9.043

2.  Mapping, cloning, cDNA sequence, and expression of the gene encoding the mouse micromolar calpain large subunit.

Authors:  C Poirier; S Poussard; D M Faust; T Imaizumi-Scherrer; M C Weiss; A Ducastaing; D Montarras; C Pinset; J L Guénet
Journal:  Mamm Genome       Date:  1998-05       Impact factor: 2.957

3.  Comparative effects between bone marrow and mesenchymal stem cell transplantation in GDNF expression and motor function recovery in a motorneuron degenerative mouse model.

Authors:  Diego Pastor; Mari Carmen Viso-León; Jonathan Jones; Jesus Jaramillo-Merchán; Juan José Toledo-Aral; Jose M Moraleda; Salvador Martínez
Journal:  Stem Cell Rev Rep       Date:  2012-06       Impact factor: 5.739

4.  Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration.

Authors:  Wolfgang M Schmidt; Cornelia Kraus; Harald Höger; Sonja Hochmeister; Felicitas Oberndorfer; Manuela Branka; Sonja Bingemann; Hans Lassmann; Markus Müller; Lúcia Inês Macedo-Souza; Mariz Vainzof; Mayana Zatz; André Reis; Reginald E Bittner
Journal:  EMBO Rep       Date:  2007-06-15       Impact factor: 8.807

5.  Bone marrow transplantation in hindlimb muscles of motoneuron degenerative mice reduces neuronal death and improves motor function.

Authors:  Diego Pastor; Mari Carmen Viso-León; Arancha Botella-López; Jesus Jaramillo-Merchan; Jose M Moraleda; Jonathan Jones; Salvador Martínez
Journal:  Stem Cells Dev       Date:  2013-02-13       Impact factor: 3.272

6.  A single nucleotide mutation in Nppc is associated with a long bone abnormality in lbab mice.

Authors:  Yan Jiao; Jian Yan; Feng Jiao; Hongbin Yang; Leah Rae Donahue; Xinmin Li; Bruce A Roe; John Stuart; Weikuan Gu
Journal:  BMC Genet       Date:  2007-04-17       Impact factor: 2.797
  6 in total

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