Literature DB >> 10444330

Genetic and physical mapping of the dreher locus on mouse chromosome 1.

D E Bergstrom1, L H Gagnon, E M Eicher.   

Abstract

Mutations in the mouse dreher (dr) gene cause skeletal defects, hyperactivity, abnormal gait, deafness, white belly spotting, and hypoplasia of Müllerian duct derivatives. To map dr to high resolution, we utilized two crosses. Initially, we analyzed an intersubspecific intercross to construct a detailed genetic map of simple sequence length polymorphism markers within a 6.3-cM region surrounding the dr locus. Subsequently, we analyzed a second intersubspecific intercross segregating for the dr(6J) allele, which positioned dr within a 0.13-cM region between Rxrg and D1Mit370. A physical contig of BAC clones spanning the dr critical region was constructed, and eight potential dr candidate genes were excluded by genetic or physical mapping. Together these results lay the foundation for positional cloning of the dr gene. Copyright 1999 Academic Press.

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Year:  1999        PMID: 10444330     DOI: 10.1006/geno.1999.5873

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  7 in total

1.  Molecular definition of an allelic series of mutations disrupting the mouse Lmx1a (dreher) gene.

Authors:  Victor Chizhikov; Ekaterina Steshina; Richard Roberts; Yesim Ilkin; Linda Washburn; Kathleen J Millen
Journal:  Mamm Genome       Date:  2006-10-03       Impact factor: 2.957

2.  Interaction with ectopic cochlear crista sensory epithelium disrupts basal cochlear sensory epithelium development in Lmx1a mutant mice.

Authors:  David H Nichols; Judith E Bouma; Benjamin J Kopecky; Israt Jahan; Kirk W Beisel; David Z Z He; Huizhan Liu; Bernd Fritzsch
Journal:  Cell Tissue Res       Date:  2020-01-13       Impact factor: 5.249

3.  Purkinje cell compartmentalization in the cerebellum of the spontaneous mutant mouse dreher.

Authors:  Roy V Sillitoe; Nicholas A George-Jones; Kathleen J Millen; Richard Hawkes
Journal:  Brain Struct Funct       Date:  2012-11-18       Impact factor: 3.270

4.  The identification of transcription factors expressed in the notochord of Ciona intestinalis adds new potential players to the brachyury gene regulatory network.

Authors:  Diana S José-Edwards; Pierre Kerner; Jamie E Kugler; Wei Deng; Di Jiang; Anna Di Gregorio
Journal:  Dev Dyn       Date:  2011-05-18       Impact factor: 3.780

Review 5.  LIM-homeodomain genes in mammalian development and human disease.

Authors:  Chad S Hunter; Simon J Rhodes
Journal:  Mol Biol Rep       Date:  2005-06       Impact factor: 2.316

6.  Mutanlallemand (mtl) and Belly Spot and Deafness (bsd) are two new mutations of Lmx1a causing severe cochlear and vestibular defects.

Authors:  Georg Steffes; Beatriz Lorente-Cánovas; Selina Pearson; Rachael H Brooker; Sarah Spiden; Amy E Kiernan; Jean-Louis Guénet; Karen P Steel
Journal:  PLoS One       Date:  2012-11-30       Impact factor: 3.240

7.  Heterozygous missense variants of LMX1A lead to nonsyndromic hearing impairment and vestibular dysfunction.

Authors:  Mieke Wesdorp; Pia A M de Koning Gans; Margit Schraders; Jaap Oostrik; Martijn A Huynen; Hanka Venselaar; Andy J Beynon; Judith van Gaalen; Vitória Piai; Nicol Voermans; Michelle M van Rossum; Bas P Hartel; Stefan H Lelieveld; Laurens Wiel; Berit Verbist; Liselotte J Rotteveel; Marieke F van Dooren; Peter Lichtner; Henricus P M Kunst; Ilse Feenstra; Ronald J C Admiraal; Helger G Yntema; Lies H Hoefsloot; Ronald J E Pennings; Hannie Kremer
Journal:  Hum Genet       Date:  2018-05-12       Impact factor: 4.132

  7 in total

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