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Brachyphalangy, an allele of extra-toes in the mouse.

作者信息

Johnson D R

出版信息

Genet Res. 1969 Jun;13(3):275-80. doi: 10.1017/s0016672300002962.

DOI:10.1017/s0016672300002962
PMID:5806166
Abstract
摘要

相似文献

1
Brachyphalangy, an allele of extra-toes in the mouse.
Genet Res. 1969 Jun;13(3):275-80. doi: 10.1017/s0016672300002962.
2
Occurrences and linkage relations of the mutant "extra-toes" in the mouse.
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3
The dominant mouse mutations fused toes (Ft) and oligosyndactylism (Os) are not allelic.显性小鼠突变融合趾(Ft)和少指(Os)并非等位基因。
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4
Genetical and embryological studies of the jt form of syndactylism in the mouse.小鼠并指畸形jt型的遗传学和胚胎学研究。
Genet Res. 1966 Aug;8(1):33-40. doi: 10.1017/s0016672300009897.
5
The development of the eye in homozygotes of the mouse mutant Extra-toes.
Anat Embryol (Berl). 1991;184(4):355-61. doi: 10.1007/BF00957897.
6
Extra-toes: anew mutant gene causing multiple abnormalities in the mouse.
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Hemimelic extra toes and Hammer toe are distinct mutations that show a genetic interaction.半侧多指(趾)畸形和槌状趾是表现出基因相互作用的不同突变。
Mamm Genome. 2001 Jan;12(1):77-9. doi: 10.1007/s003350010235.
8
Teratogenesis of acetazolamide in the CBA/J and SWV strains of mice. II. Genetic control of the teratogenic response.
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Gli3 expression is affected in the morphogenetic mouse mutants add and Xt.Gli3基因的表达在形态发生小鼠突变体add和Xt中受到影响。
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The independent assortment of dominant white and polydactyly in the cat.猫中显性白色基因和多指基因的独立分配。
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引用本文的文献

1
Interfrontal Bone Among Inbred Strains of Mice and QTL Mapping.小鼠近交系间的额骨及数量性状基因座定位
Front Genet. 2019 Apr 2;10:291. doi: 10.3389/fgene.2019.00291. eCollection 2019.
2
Ectodermal influx and cell hypertrophy provide early growth for all murine mammary rudiments, and are differentially regulated among them by Gli3.外胚层流入和细胞肥大为所有小鼠乳腺原基提供早期生长,并由 Gli3 在它们之间进行差异调节。
PLoS One. 2011;6(10):e26242. doi: 10.1371/journal.pone.0026242. Epub 2011 Oct 27.
3
Defective ciliogenesis, embryonic lethality and severe impairment of the Sonic Hedgehog pathway caused by inactivation of the mouse complex A intraflagellar transport gene Ift122/Wdr10, partially overlapping with the DNA repair gene Med1/Mbd4.
小鼠复合A鞭毛内运输基因Ift122/Wdr10失活导致纤毛发生缺陷、胚胎致死以及音猬因子信号通路严重受损,该基因与DNA修复基因Med1/Mbd4部分重叠。
Dev Biol. 2009 Jan 1;325(1):225-37. doi: 10.1016/j.ydbio.2008.10.020. Epub 2008 Oct 29.
4
Signaling through Tgf-beta type I receptor Alk5 is required for upper lip fusion.通过转化生长因子-β I型受体Alk5发出的信号是上唇融合所必需的。
Mech Dev. 2008 Sep-Oct;125(9-10):874-82. doi: 10.1016/j.mod.2008.06.003. Epub 2008 Jun 11.
5
The cleft lip and palate defects in Dancer mutant mice result from gain of function of the Tbx10 gene.舞者突变小鼠的唇腭裂缺陷是由Tbx10基因的功能获得所致。
Proc Natl Acad Sci U S A. 2004 May 4;101(18):7022-7. doi: 10.1073/pnas.0401025101. Epub 2004 Apr 26.
6
The development of the eye in homozygotes of the mouse mutant Extra-toes.
Anat Embryol (Berl). 1991;184(4):355-61. doi: 10.1007/BF00957897.
7
Mouse chromosome 13.小鼠13号染色体。
Mamm Genome. 1991;1 Spec No:S205-20. doi: 10.1007/BF00656494.
8
Splotch locus mouse mutants: models for neural tube defects and Waardenburg syndrome type I in humans.斑点基因座小鼠突变体:人类神经管缺陷和I型瓦登伯革氏综合征的模型
J Med Genet. 1992 Mar;29(3):145-51. doi: 10.1136/jmg.29.3.145.
9
Mouse chromosome 13.小鼠13号染色体。
Mamm Genome. 1992;3 Spec No:S195-205. doi: 10.1007/BF00648431.
10
The interfrontal bone and mutant genes in the mouse.小鼠的额间骨与突变基因。
J Anat. 1976 Jul;121(Pt 3):507-13.