Literature DB >> 29444210

The recurrent mutation in TMEM106B also causes hypomyelinating leukodystrophy in China and is a CpG hotspot.

Huifang Yan1,2, Thomas Kubisiak2, Haoran Ji1, Jiangxi Xiao3, Jingmin Wang1, Margit Burmeister2,4.   

Abstract

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Year:  2018        PMID： 29444210     DOI： 10.1093/brain/awy029

Source DB:  PubMed          Journal:  Brain        ISSN： 0006-8950            Impact factor:   13.501


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  10 in total

1.  A role of the frontotemporal lobar degeneration risk factor TMEM106B in myelination.

Authors:  Tuancheng Feng; Rory R Sheng; Santiago Solé-Domènech; Mohammed Ullah; Xiaolai Zhou; Christina S Mendoza; Laura Camila Martinez Enriquez; Isabel Iscol Katz; Daniel H Paushter; Peter M Sullivan; Xiaochun Wu; Frederick R Maxfield; Fenghua Hu
Journal:  Brain       Date:  2020-07-01       Impact factor: 13.501

Review 2.  The lysosomal function of progranulin, a guardian against neurodegeneration.

Authors:  Daniel H Paushter; Huan Du; Tuancheng Feng; Fenghua Hu
Journal:  Acta Neuropathol       Date:  2018-05-09       Impact factor: 17.088

3.  Recent advances in the genetics of frontotemporal dementia.

Authors:  Daniel W Sirkis; Ethan G Geier; Luke W Bonham; Celeste M Karch; Jennifer S Yokoyama
Journal:  Curr Genet Med Rep       Date:  2019-01-30

Review 4.  The Role of Microglia in Inherited White-Matter Disorders and Connections to Frontotemporal Dementia.

Authors:  Daniel W Sirkis; Luke W Bonham; Jennifer S Yokoyama
Journal:  Appl Clin Genet       Date:  2021-03-31

5.  TMEM106B deficiency impairs cerebellar myelination and synaptic integrity with Purkinje cell loss.

Authors:  Tuancheng Feng; Lin Luan; Isabel Iscol Katz; Mohammed Ullah; Vivianna M Van Deerlin; John Q Trojanowski; Edward B Lee; Fenghua Hu
Journal:  Acta Neuropathol Commun       Date:  2022-03-14       Impact factor: 7.801

6.  Severe Epilepsy and Movement Disorder May Be Early Symptoms of TMEM106B-Related Hypomyelinating Leukodystrophy.

Authors:  Roberta Solazzi; Marco Moscatelli; Davide Rossi Sebastiano; Laura Canafoglia; Laura Pezzoli; Maria Iascone; Tiziana Granata
Journal:  Neurol Genet       Date:  2022-08-29

Review 7.  Physiological and pathological functions of TMEM106B: a gene associated with brain aging and multiple brain disorders.

Authors:  Tuancheng Feng; Alexander Lacrampe; Fenghua Hu
Journal:  Acta Neuropathol       Date:  2021-01-01       Impact factor: 17.088

8.  Loss of TMEM106B and PGRN leads to severe lysosomal abnormalities and neurodegeneration in mice.

Authors:  Tuancheng Feng; Shuyi Mai; Jenn Marie Roscoe; Rory R Sheng; Mohammed Ullah; Junke Zhang; Isabel Iscol Katz; Haiyuan Yu; Wenjun Xiong; Fenghua Hu
Journal:  EMBO Rep       Date:  2020-08-10       Impact factor: 8.807

Review 9.  The Role of White Matter Dysfunction and Leukoencephalopathy/Leukodystrophy Genes in the Aetiology of Frontotemporal Dementias: Implications for Novel Approaches to Therapeutics.

Authors:  Hiu Chuen Lok; John B Kwok
Journal:  Int J Mol Sci       Date:  2021-03-03       Impact factor: 5.923

10.  Aged Tmem106b knockout mice display gait deficits in coincidence with Purkinje cell loss and only limited signs of non-motor dysfunction.

Authors:  Stijn Stroobants; Rudi D'Hooge; Markus Damme
Journal:  Brain Pathol       Date:  2020-11-01       Impact factor: 6.508
  10 in total

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