A mouse model for human hereditary tyrosinemia I.

A mouse model for human hereditary tyrosinemia I.
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人类遗传性酪氨酸血症 I 的小鼠模型。

DOI:
10.1002/bies.950160203
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发表时间:
1994
期刊:
BioEssays : news and reviews in molecular, cellular and developmental biology
影响因子:
--
通讯作者:
T. Magnuson
T. Magnuson
中科院分区:
--
文献类型:
--
作者:
B. Holdener;T. Magnuson

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Figure 1. Above: Map of the albino region on chromosome 7. This map is a subset of the complementation map presented by Russell et~ l.(~). Marker loci are indicated above the map and include: tp (taupe), c (albino= tyrosinase), Mod-2 (mitochondria1 form of malic enzyme) and sh-I. Functional units defined by genetic complementation of albino deletions are indicated below the map and include msd (mesoderm deficient), hsdr-1 (hepatocyte-specific developmental regulator-l= Fuh), jdf (juvenile development and fertility), eed (embryonic ectoderm development) and exed (extra-embryonic ectoderm development). Deletions from the E, A, and Bem complementation group are shown. The number of deletions in the group is indicated in parenthesis. Gaps indicate the deleted regions. Below: Expansion of the region spanning msd and hsdr-I. The physical size of the hsdr-1 region is estimated to be 3 10 kb (22, 23). The size of the region of non-overlap between c~~ and c14c0s is not known. Specific deletion names are indicated and complementation groups shown in parenthesis. The dH deletion was not part of the original complementation analysis involving the other 34 albino deletions (3) but was assigned to the E group (38) on the basis of a smaller complementation analysis conducted by Gluecks~ hn-Waelsch (~).
对小鼠白化缺失复合物进行物理定位,以定位 alf/hsdr-1(新生儿存活所需的基因座)。
DOI: 10.1016/s0888-7543(05)80217-4
发表时间: 1992
期刊: Genomics
影响因子: 4.4
作者:
Kelsey,G;Schedl,A;Ruppert,S;Niswander,L;Magnuson,T;Klebig,ML;Rinchik,EM;Schütz,G
通讯作者: Schütz,G
从侧翼标记的染色体跳跃定义了白化缺失复合体中 alf/hsdr-1 的最小区域。
DOI: 10.1016/s0888-7543(05)80218-6
发表时间: 1992
期刊: Genomics
影响因子: 4.4
作者:
Schedl,A;Ruppert,S;Kelsey,G;Thies,E;Niswander,L;Magnuson,T;Klebig,ML;Rinchik,EM;Schütz,G
通讯作者: Schütz,G
肝肾酪氨酸血症小鼠模型的代谢研究:不存在围产期异常。
DOI: 10.1016/s0006-291x(05)81498-6
发表时间: 1992
影响因子: 3.1
作者:
Collins,JC;Buchanan,DN;Thoene,JG;Erickson,RP;Brooks,SS;Gluecksohn-Waelsch,S
通讯作者: Gluecksohn-Waelsch,S
与小鼠早期胚胎致死相关的白化缺失的分子图谱。
DOI: 10.1016/0888-7543(91)90234-6
发表时间: 1991
期刊: Genomics
影响因子: 4.4
作者:
Niswander,L;Kelsey,G;Schedl,A;Ruppert,S;Sharan,SK;Holdener-Kenny,B;Rinchik,EM;Edström,JE;Magnuson,T
通讯作者: Magnuson,T
DOI: 10.1101/gad.7.12a.2298
发表时间: 1993-12-01
影响因子: 10.5
作者:
GROMPE, M;ALDHALIMY, M;SORIANO, P
通讯作者: SORIANO, P