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Assignment of the paired box gene Pax1 to rat chromosome 3.

作者信息

Otsen M, Balling R, Den Bieman M, Van Zutphen L F

机构信息

Department of Laboratory Animal Science, Faculty of Veterinary Medicine, Utrecht University, The Netherlands.

出版信息

Mamm Genome. 1995 Sep;6(9):666-7. doi: 10.1007/BF00352378.

DOI:10.1007/BF00352378
PMID:8535079
Abstract
摘要

相似文献

1
Assignment of the paired box gene Pax1 to rat chromosome 3.
Mamm Genome. 1995 Sep;6(9):666-7. doi: 10.1007/BF00352378.
2
Pax1, a member of the paired box-containing class of developmental control genes, is mapped to human chromosome 20p11.2 by in situ hybridization (ISH and FISH).
Genomics. 1992 Nov;14(3):740-4. doi: 10.1016/s0888-7543(05)80177-6.
3
Characterization and developmental expression of Pax9, a paired-box-containing gene related to Pax1.Pax9的特征及发育表达，Pax9是一个与Pax1相关的含配对盒基因。
Dev Biol. 1995 Aug;170(2):701-16. doi: 10.1006/dbio.1995.1248.
4
A genetic linkage map of mouse chromosome 2 extending from thrombospondin to paired box gene 1, including the H3 minor histocompatibility complex.
Genomics. 1996 Apr 1;33(1):75-84. doi: 10.1006/geno.1996.0161.
5
Characterization of a novel insertional mouse mutation, kkt: A closely linked modifier of Pax1.一种新型插入性小鼠突变体kkt的特征：Pax1的紧密连锁修饰基因。
Dev Biol. 2000 Feb 15;218(2):354-66. doi: 10.1006/dbio.1999.9584.
6
Mutations in PAX1 may be associated with Klippel-Feil syndrome.PAX1基因的突变可能与克-费二氏综合征有关。
Eur J Hum Genet. 2003 Jun;11(6):468-74. doi: 10.1038/sj.ejhg.5200987.
7
Assignment of the canine paired-box 3 (PAX3) gene to chromosome 37q16-->q17 by in situ hybridization.
Cytogenet Cell Genet. 2000;90(1-2):66-7. doi: 10.1159/000015664.
8
Evolutionary conservation of gene structures of the Pax1/9 gene family.
Biochim Biophys Acta. 2000 Jul 24;1492(2-3):517-21. doi: 10.1016/s0167-4781(00)00130-5.
9
Altered regulation of platelet-derived growth factor receptor-alpha gene-transcription in vitro by spina bifida-associated mutant Pax1 proteins.脊柱裂相关突变型Pax1蛋白在体外对血小板衍生生长因子受体α基因转录的调控改变
Proc Natl Acad Sci U S A. 1998 Nov 24;95(24):14459-63. doi: 10.1073/pnas.95.24.14459.
10
Pax1 and Pax9 activate Bapx1 to induce chondrogenic differentiation in the sclerotome.Pax1和Pax9激活Bapx1以诱导体节中软骨生成分化。
Development. 2003 Feb;130(3):473-82. doi: 10.1242/dev.00240.

本文引用的文献

1
A rat genetic linkage map and comparative maps for mouse or human homologous rat genes.一张大鼠遗传连锁图谱以及小鼠或人类同源大鼠基因的比较图谱。
Mamm Genome. 1994 Feb;5(2):63-83. doi: 10.1007/BF00292332.
2
A genetic linkage map of the laboratory rat, Rattus norvegicus.实验大鼠褐家鼠的遗传连锁图谱。
Nat Genet. 1995 Jan;9(1):63-9. doi: 10.1038/ng0195-63.
3
undulated, a mutation affecting the development of the mouse skeleton, has a point mutation in the paired box of Pax 1.波状（undulated）是一种影响小鼠骨骼发育的突变，它在Pax 1的配对盒中有一个点突变。
Cell. 1988 Nov 4;55(3):531-5. doi: 10.1016/0092-8674(88)90039-6.
4
Conservation of a large protein domain in the segmentation gene paired and in functionally related genes of Drosophila.果蝇体节基因“配对”及功能相关基因中一个大蛋白质结构域的保守性。
Cell. 1986 Dec 26;47(6):1033-40. doi: 10.1016/0092-8674(86)90818-4.
5
Pax 1, a member of a paired box homologous murine gene family, is expressed in segmented structures during development.Pax 1是配对盒同源鼠基因家族的成员之一，在发育过程中表达于分节结构中。
Cell. 1988 May 20;53(4):617-25. doi: 10.1016/0092-8674(88)90577-6.
6
The gene map of the Norway rat (Rattus norvegicus) and comparative mapping with mouse and man.褐家鼠（Rattus norvegicus）的基因图谱以及与小鼠和人类的比较图谱。
Genomics. 1991 Jul;10(3):699-718. doi: 10.1016/0888-7543(91)90455-n.
7
The molecular basis of the undulated/Pax-1 mutation.波状/配对盒基因1（Pax-1）突变的分子基础。
Cell. 1991 Sep 6;66(5):873-84. doi: 10.1016/0092-8674(91)90434-z.
8
The paired box encodes a second DNA-binding domain in the paired homeo domain protein.配对盒在配对同源域蛋白中编码第二个DNA结合结构域。
Genes Dev. 1991 Apr;5(4):594-604. doi: 10.1101/gad.5.4.594.
9
Rat gene mapping using PCR-analyzed microsatellites.利用聚合酶链反应分析的微卫星进行大鼠基因定位。
Genetics. 1992 Jul;131(3):701-21. doi: 10.1093/genetics/131.3.701.
10
Pax1, a member of the paired box-containing class of developmental control genes, is mapped to human chromosome 20p11.2 by in situ hybridization (ISH and FISH).
Genomics. 1992 Nov;14(3):740-4. doi: 10.1016/s0888-7543(05)80177-6.