Literature DB >> 6681440

The murine mutation trembler-J: proof of semidominant expression by use of the linked vestigial tail marker.

E W Henry, R L Sidman.   

Abstract

Trembler-J, TrJ, is a peripheral hypomyelinating murine mutant. In intercrosses (TrJ/ + X TrJ/ +) there are severely affected (behaviorally and pathologically), mildly affected, and normal offspring, while backcrosses (TrJ/ + X + / +) produce only mildly affected and normal offspring. We used the closely linked marker vestigial tail, vt, to test whether severely affected offspring of intercrosses (TrJvt/ + + X TrJvt/ + +) were TrJ/TrJ. In 5/6 intercrosses all severely affected animals were short-tailed and vice versa, while all mildly affected animals had long tails and vice versa. It is highly probable that the severely affected, mildly affected, and normal classes of intercross offspring were of TrJ/TrJ, TrJ/+, and +/+ genotypes, respectively.

Entities:  

Mesh:

Year:  1983        PMID: 6681440     DOI: 10.3109/01677068309107071

Source DB:  PubMed          Journal:  J Neurogenet        ISSN: 0167-7063            Impact factor:   1.250


  9 in total

1.  Differential aggregation of the Trembler and Trembler J mutants of peripheral myelin protein 22.

Authors:  Andreas R Tobler; Ning Liu; Lukas Mueller; Eric M Shooter
Journal:  Proc Natl Acad Sci U S A       Date:  2001-12-18       Impact factor: 11.205

2.  Structural and Functional Abnormalities of the Neuromuscular Junction in the Trembler-J Homozygote Mouse Model of Congenital Hypomyelinating Neuropathy.

Authors:  Alexandra N Scurry; Dante J Heredia; Cheng-Yuan Feng; Gregory B Gephart; Grant W Hennig; Thomas W Gould
Journal:  J Neuropathol Exp Neurol       Date:  2016-02-25       Impact factor: 3.685

3.  Upregulation of the endosomal-lysosomal pathway in the trembler-J neuropathy.

Authors:  L Notterpek; E M Shooter; G J Snipes
Journal:  J Neurosci       Date:  1997-06-01       Impact factor: 6.167

4.  Transport of Trembler-J mutant peripheral myelin protein 22 is blocked in the intermediate compartment and affects the transport of the wild-type protein by direct interaction.

Authors:  A R Tobler; L Notterpek; R Naef; V Taylor; U Suter; E M Shooter
Journal:  J Neurosci       Date:  1999-03-15       Impact factor: 6.167

5.  Long-term analyses of innervation and neuromuscular integrity in the Trembler-J mouse model of Charcot-Marie-Tooth disease.

Authors:  Jessica Renee Nicks; Sooyeon Lee; Kathryne Ann Kostamo; Andrew Benford Harris; Amanda M Sookdeo; Lucia Notterpek
Journal:  J Neuropathol Exp Neurol       Date:  2013-10       Impact factor: 3.685

6.  A leucine-to-proline mutation in the putative first transmembrane domain of the 22-kDa peripheral myelin protein in the trembler-J mouse.

Authors:  U Suter; J J Moskow; A A Welcher; G J Snipes; B Kosaras; R L Sidman; A M Buchberg; E M Shooter
Journal:  Proc Natl Acad Sci U S A       Date:  1992-05-15       Impact factor: 11.205

7.  Rer1 and calnexin regulate endoplasmic reticulum retention of a peripheral myelin protein 22 mutant that causes type 1A Charcot-Marie-Tooth disease.

Authors:  Taichi Hara; Yukiko Hashimoto; Tomoko Akuzawa; Rika Hirai; Hisae Kobayashi; Ken Sato
Journal:  Sci Rep       Date:  2014-11-11       Impact factor: 4.379

8.  Central Alteration in Peripheral Neuropathy of Trembler-J Mice: Hippocampal pmp22 Expression and Behavioral Profile in Anxiety Tests.

Authors:  Juan Pablo Damián; Lucia Vázquez Alberdi; Lucía Canclini; Gonzalo Rosso; Silvia Olivera Bravo; Mariana Martínez; Natalia Uriarte; Paul Ruiz; Miguel Calero; María Vittoria Di Tomaso; Alejandra Kun
Journal:  Biomolecules       Date:  2021-04-19

9.  Colocalization Analysis of Peripheral Myelin Protein-22 and Lamin-B1 in the Schwann Cell Nuclei of Wt and TrJ Mice.

Authors:  María Vittoria Di Tomaso; Lucía Vázquez Alberdi; Daniela Olsson; Saira Cancela; Anabel Fernández; Juan Carlos Rosillo; Ana Laura Reyes Ábalos; Magdalena Álvarez Zabaleta; Miguel Calero; Alejandra Kun
Journal:  Biomolecules       Date:  2022-03-16
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.