HoxB2 binds mutant SOD1 and is altered in transgenic model of ALS. (Q40389314)

20 September 2017

title

HoxB2 binds mutant SOD1 and is altered in transgenic model of ALS. (English)

1 reference

amyotrophic lateral sclerosis

20 September 2017

main subject

1 reference

Jinbin Zhai

1

1 reference

20 September 2017

Hong Lin

series ordinal

2

1 reference

20 September 2017

Rafaela Canete-Soler

series ordinal

3

1 reference

20 September 2017

William W Schlaepfer

series ordinal

4

1 reference

20 September 2017

publication date

3 August 2005

1 reference

20 September 2017

published in

Human Molecular Genetics

1 reference

20 September 2017

volume

14

1 reference

20 September 2017

issue

18

1 reference

20 September 2017

page(s)

2629-2640

1 reference

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

20 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Mutant SOD1 alters the motor neuronal transcriptome: implications for familial ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Sodium phenylbutyrate prolongs survival and regulates expression of anti-apoptotic genes in transgenic amyotrophic lateral sclerosis mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Homeobox genes and axial patterning

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Homeobox gene expression profile in human hematopoietic multipotent stem cells and T-cell progenitors: implications for human T-cell development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

HOX homeobox genes exhibit spatial and temporal changes in expression during human skin development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Coordinated expression of 3' hox genes during murine embryonal gut development: an enteric Hox code

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Region-specific gastrointestinal Hox code during murine embryonal gut development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Differentiation phenotypes of pancreatic islet beta- and alpha-cells are closely related with homeotic genes and a group of differentially expressed genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Expression of Hox cofactor genes during mouse ovarian follicular development and oocyte maturation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

The role of HOX genes in the development and function of the female reproductive tract

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Homeobox genes and male reproductive development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Hox genes and spinal cord development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Assigning the positional identity of spinal motor neurons: rostrocaudal patterning of Hox-c expression by FGFs, Gdf11, and retinoids.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Comprehensive expression profiling of highly homologous 39 hox genes in 26 different human adult tissues by the modified systematic multiplex RT-pCR method reveals tissue-specific expression pattern that suggests an important role of chromosomal str

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Expression profiles of 39 HOX genes in normal human adult organs and anaplastic thyroid cancer cell lines by quantitative real-time RT-PCR system

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Mutations in SOD1 associated with amyotrophic lateral sclerosis cause novel protein interactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

ALS-linked SOD1 mutant G85R mediates damage to astrocytes and promotes rapidly progressive disease with SOD1-containing inclusions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Aggregation and Motor Neuron Toxicity of an ALS-Linked SOD1 Mutant Independent from Wild-Type SOD1

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

New consensus research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 (SOD1) gene mutations: inclusions containing SOD1 in neurons and astrocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Mutant Cu/Zn-superoxide dismutase proteins have altered solubility and interact with heat shock/stress proteins in models of amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Formation of high molecular weight complexes of mutant Cu, Zn-superoxide dismutase in a mouse model for familial amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Mutations associated with amyotrophic lateral sclerosis convert superoxide dismutase from an antiapoptotic gene to a proapoptotic gene: studies in yeast and neural cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

The zinc finger gene Krox20 regulates HoxB2 (Hox2.8) during hindbrain segmentation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Protein aggregation and aggregate toxicity: new insights into protein folding, misfolding diseases and biological evolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Assembly of A beta amyloid protofibrils: an in vitro model for a possible early event in Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Pivotal role of oligomerization in expanded polyglutamine neurodegenerative disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

3' untranslated region in a light neurofilament (NF-L) mRNA triggers aggregation of NF-L and mutant superoxide dismutase 1 proteins in neuronal cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Dorfin ubiquitylates mutant SOD1 and prevents mutant SOD1-mediated neurotoxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

NEDL1, a novel ubiquitin-protein isopeptide ligase for dishevelled-1, targets mutant superoxide dismutase-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

CHIP promotes proteasomal degradation of familial ALS-linked mutant SOD1 by ubiquitinating Hsp/Hsc70.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Amyotrophic lateral sclerosis-associated SOD1 mutant proteins bind and aggregate with Bcl-2 in spinal cord mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Alsin, the product of ALS2 gene, suppresses SOD1 mutant neurotoxicity through RhoGEF domain by interacting with SOD1 mutants

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Amyloid-like filaments and water-filled nanotubes formed by SOD1 mutant proteins linked to familial ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Hoxa10 and Hoxd10 coordinately regulate lumbar motor neuron patterning

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Altered segmental identity and abnormal migration of motor neurons in mice lacking Hoxb-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Hox genes and the identity of motor neurons in the hindbrain

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Coordinated temporal and spatial control of motor neuron and serotonergic neuron generation from a common pool of CNS progenitors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

HOX genes in human lung: altered expression in primary pulmonary hypertension and emphysema

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Homeobox genes and cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Mutation of HOXA13 in hand-foot-genital syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

A HOX gene mutation in a family with isolated congenital vertical talus and Charcot-Marie-Tooth disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Molecular cell biology of Charcot-Marie-Tooth disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

Direct Interaction of Focal Adhesion Kinase with p190RhoGEF

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDI297

21 January 2018

Identifiers

DOI

10.1093/HMG/DDI297

1 reference

release_rget6ainhnepjesv5ik4ax44vm

20 September 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/rget6ainhnepjesv5ik4ax44vm

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference