家鼠（小家鼠）中具有神经学效应的两个新突变体，“颤抖者”和“旋转者”。 - Suppr

Suppr

超能文献

Two new mutants, 'trembler' and 'reeler', with neurological actions in the house mouse (Mus musculus L.).

作者信息

FALCONER D S

出版信息

J Genet. 1951 Jan;50(2):192-201. doi: 10.1007/BF02996215.

DOI:10.1007/BF02996215

PMID:24539699

Abstract

摘要

相似文献

Two new mutants, 'trembler' and 'reeler', with neurological actions in the house mouse (Mus musculus L.).

J Genet. 1951 Jan;50(2):192-201. doi: 10.1007/BF02996215.

Neurological actions caused by the mutant gene Trembler in the house mouse (Mus musculus, L.,) an investigation.

J Neuropathol Exp Neurol. 1953 Jan;12(1):64-72. doi: 10.1097/00005072-195301000-00006.

[HEREDITARY ATAXIA WITH UNUSUALLY MARKED SPASTIC FACTORS, WITH SPECIAL REFERENCE TO ITS RELATION TO HEREDITARY SPASTIC SPINAL PARALYSIS].

Seishin Shinkeigaku Zasshi. 1963 Sep;65:763-77.

Genetic study of the Ku. family, affected with familial spastic spinal paralysis. The mode of transmission of this affection.

J Genet Hum. 1959 Oct;8:169-78.

[On first manifestations of spastic spinal paralysis in old age].

Nervenarzt. 1961 Apr;32:183-6.

[Familial spastic paralysis (Struempell-Lorrain disease)].

An Fac Med Univ Repub Montev Urug. 1960;45:115-24.

[Clinical observations on genetic factors in hereditary spastic spinal paralysis with anteposition until early childhood].

Wien Z Nervenheilkd Grenzgeb. 1960;18:95-102.

Inheritance of a spastic lethal in cattle.

J Hered. 1962 May-Jun;53:130-2. doi: 10.1093/oxfordjournals.jhered.a107146.

Interaction of cerebellar mutant genes. II. Mice doubly affected by 'reeler' and 'weaver' conditions.

Brain Res. 1975 Oct 17;96(2):219-32. doi: 10.1016/0006-8993(75)90732-5.

[Cerebellar ataxia with spasticity. Report of 4 cases, including 3 in the same family].

Rev Esp Pediatr. 1963 Mar-Apr;19:151-6.

引用本文的文献

Reelin Controls the Directional Orientation, Apical Localization and Length of Primary Cilia in Principal Neurons in the Cerebral Cortex.

bioRxiv. 2025 Aug 24:2025.08.24.672028. doi: 10.1101/2025.08.24.672028.

Genetic influence of a STAU2 frameshift mutation and RELN regulatory elements on performance in Icelandic horses.

Sci Rep. 2025 Apr 4;15(1):11641. doi: 10.1038/s41598-025-95593-8.

Reelin marks cocaine-activated striatal neurons, promotes neuronal excitability, and regulates cocaine reward.

Sci Adv. 2025 Mar 28;11(13):eads4441. doi: 10.1126/sciadv.ads4441. Epub 2025 Mar 26.

Genetic or therapeutic disruption of the Reelin/Apoer2 signaling pathway improves inflammatory arthritis outcomes.

Proc Natl Acad Sci U S A. 2025 Mar 18;122(11):e2418642122. doi: 10.1073/pnas.2418642122. Epub 2025 Mar 12.

Cerebellar nuclei cells produce distinct pathogenic spike signatures in mouse models of ataxia, dystonia, and tremor.

Elife. 2024 Jul 29;12:RP91483. doi: 10.7554/eLife.91483.

De novo monoallelic Reelin missense variants cause dominant neuronal migration disorders via a dominant-negative mechanism.

J Clin Invest. 2024 Jul 9;134(16):e153097. doi: 10.1172/JCI153097.

Safety of Anti-Reelin Therapeutic Approaches for Chronic Inflammatory Diseases.

Cells. 2024 Mar 27;13(7):583. doi: 10.3390/cells13070583.

Molecular Mechanisms of Reelin in the Enteric Nervous System and the Microbiota-Gut-Brain Axis: Implications for Depression and Antidepressant Therapy.

Int J Mol Sci. 2024 Jan 9;25(2):814. doi: 10.3390/ijms25020814.

Cerebellar dysfunction in rodent models with dystonia, tremor, and ataxia.

Dystonia. 2023;2. doi: 10.3389/dyst.2023.11515. Epub 2023 Dec 8.

The genetics of gaits in Icelandic horses goes beyond DMRT3, with RELN and STAU2 identified as two new candidate genes.

Genet Sel Evol. 2023 Dec 11;55(1):89. doi: 10.1186/s12711-023-00863-6.

本文引用的文献

Mutations induced in Coprinus fimetarius (L) by nitrogen mustard.

Nature. 1948 Nov 27;162(4126):846. doi: 10.1038/162846a0.

Heterocaryosis in Neurospora Crassa.

Genetics. 1944 May;29(3):291-308. doi: 10.1093/genetics/29.3.291.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验