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The clf1 gene maps to a 2- to 3-cM region of distal mouse chromosome 11.

作者信息

Juriloff D M, Harris M J, Mah D G

机构信息

Department of Medical Genetics, University of British Columbia, 6174 University Boulevard, Vancouver, British Columbia, V6T 1Z3, Canada.

出版信息

Mamm Genome. 1996 Oct;7(10):789. doi: 10.1007/s003359900298.

DOI:10.1007/s003359900298
PMID:8854874
Abstract
摘要

相似文献

1
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2
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Wnt9b is the mutated gene involved in multifactorial nonsyndromic cleft lip with or without cleft palate in A/WySn mice, as confirmed by a genetic complementation test.经基因互补试验证实，Wnt9b是A/WySn小鼠中与伴有或不伴有腭裂的多因素非综合征性唇裂相关的突变基因。
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6
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Characterization of a novel gene disrupted by a balanced chromosomal translocation t(2;19)(q11.2;q13.3) in a family with cleft lip and palate.一个唇腭裂家族中由平衡染色体易位t(2;19)(q11.2;q13.3)破坏的新基因的特征分析。
Genomics. 1998 Dec 1;54(2):231-40. doi: 10.1006/geno.1998.5577.

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The A-kinase Anchoring Protein GSKIP Regulates GSK3β Activity and Controls Palatal Shelf Fusion in Mice.A激酶锚定蛋白GSKIP调节GSK3β活性并控制小鼠的腭突融合。
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3
Application of a novel hybrid study design to explore gene-environment interactions in orofacial clefts.

本文引用的文献

1
Encyclopedia of the mouse genome V. Mouse chromosome 11.
Mamm Genome. 1996;6 Spec No:S201-20.
2
Further evidence of a relationship between the retinoic acid receptor alpha locus and nonsyndromic cleft lip with or without cleft palate (CL +/- P).视黄酸受体α基因座与非综合征性唇裂伴或不伴腭裂（CL +/- P）之间关系的进一步证据。
Am J Hum Genet. 1993 Nov;53(5):1156-7.
3
The alymphoplasia (aly) mutation co-segregates with the intercellular adhesion molecule-2 (lcam-2) on mouse chromosome 11.无淋巴细胞形成（aly）突变与小鼠11号染色体上的细胞间黏附分子2（Icam-2）共分离。
一种新型混合研究设计在探索口腔颌面裂隙基因-环境相互作用中的应用。
Ann Hum Genet. 2012 May;76(3):221-36. doi: 10.1111/j.1469-1809.2012.00707.x.
4
Palatogenesis: engineering, pathways and pathologies.腭发生：工程、途径和病理学。
Organogenesis. 2011 Oct-Dec;7(4):242-54. doi: 10.4161/org.7.4.17926. Epub 2011 Oct 1.
5
The emerging face of primary cilia.初级纤毛的新面貌。
Genesis. 2011 Apr;49(4):231-46. doi: 10.1002/dvg.20728. Epub 2011 Apr 1.
6
Expression of Wnt9b and activation of canonical Wnt signaling during midfacial morphogenesis in mice.小鼠面中部形态发生过程中Wnt9b的表达及经典Wnt信号通路的激活
Dev Dyn. 2006 May;235(5):1448-54. doi: 10.1002/dvdy.20723.
7
Development of the upper lip: morphogenetic and molecular mechanisms.上唇的发育：形态发生和分子机制
Dev Dyn. 2006 May;235(5):1152-66. doi: 10.1002/dvdy.20646.
Int Immunol. 1994 Jul;6(7):991-4. doi: 10.1093/intimm/6.7.991.
4
A genetic map of the mouse with 4,006 simple sequence length polymorphisms.一张具有4006个简单序列长度多态性的小鼠遗传图谱。
Nat Genet. 1994 Jun;7(2 Spec No):220-45. doi: 10.1038/ng0694supp-220.
5
The major locus for multifactorial nonsyndromic cleft lip maps to mouse chromosome 11.多因素非综合征性唇裂的主要基因座定位于小鼠11号染色体。
Mamm Genome. 1995 Feb;6(2):63-9. doi: 10.1007/BF00303246.
6
Genetic analysis of the construction of the AEJ.A congenic strain indicates that nonsyndromic CL(P) in the mouse is caused by two loci with epistatic interaction.AEJ构建的遗传分析。一个同源近交系表明，小鼠的非综合征性CL(P)由两个具有上位性相互作用的基因座引起。
J Craniofac Genet Dev Biol. 1995 Jan-Mar;15(1):1-12.
7
Cleft lip with or without cleft palate: associations with transforming growth factor alpha and retinoic acid receptor loci.唇裂伴或不伴腭裂：与转化生长因子α及视黄酸受体基因座的关联
Am J Hum Genet. 1992 Dec;51(6):1377-85.