(Q34634070)

English

SEPT9 sequence alternations causing hereditary neuralgic amyotrophy are associated with altered interactions with SEPT4/SEPT11 and resistance to Rho/Rhotekin-signaling

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scholarly article

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Europe PubMed Central

PubMed publication ID

3 August 2017

SEPT9 sequence alternations causing hereditary neuralgic amyotrophy are associated with altered interactions with SEPT4/SEPT11 and resistance to Rho/Rhotekin-signaling (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Hereditary neuralgic amyotrophy

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author name string

Kaori Sudo

1

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Hidenori Ito

2

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Ikuko Iwamoto

3

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Rika Morishita

4

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Tomiko Asano

5

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3 August 2017

Koh-ichi Nagata

6

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3 August 2017

publication date

1 October 2007

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Europe PubMed Central

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3 August 2017

1 reference

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3 August 2017

28

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3 August 2017

10

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

1005-1013

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Assembly of Mammalian Septins

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20554

21 January 2018

Establishment, characterization, and evolution of cultures enriched in type-2 astrocytes

1 reference

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7 January 2021

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Rho GTPases in cell biology

1 reference

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A cryotomic method of hemisecting insect appendages for neuro-immunohistology

1 reference

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The role of the Rho GTPases in neuronal development

1 reference

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The pathobiology of the septin gene family

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20554

7 January 2021

based on heuristic

inferred from DOI database lookup

Biochemical and cell biological characterization of a mammalian septin, Sept11.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20554

7 January 2021

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Genetic control of the cell division cycle in yeast *1IV. Genes controlling bud emergence and cytokinesis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20554

7 January 2021

based on heuristic

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Possible role of Rho/Rhotekin signaling in mammalian septin organization

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20554

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Rho GTPases in transformation and metastasis.

1 reference

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Genomic and expression analyses of alternatively spliced transcripts of the MLL septin-like fusion gene (MSF) that map to a 17q25 region of loss in breast and ovarian tumors

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20554

7 January 2021

based on heuristic

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Diversity of septin scaffolds

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20554

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in SEPT9 cause hereditary neuralgic amyotrophy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20554

7 January 2021

based on heuristic

inferred from DOI database lookup

Human septin-septin interactions as a prerequisite for targeting septin complexes in the cytosol

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20554

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutation analysis of 4 candidate genes for hereditary neuralgic amyotrophy (HNA).

1 reference

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7 January 2021

based on heuristic

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TGF-beta induced transdifferentiation of mammary epithelial cells to mesenchymal cells: involvement of type I receptors

1 reference

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7 January 2021

based on heuristic

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Filament formation of MSF-A, a mammalian septin, in human mammary epithelial cells depends on interactions with microtubules

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20554

7 January 2021

based on heuristic

inferred from DOI database lookup

Biochemical and cell biological analyses of a mammalian septin complex, Sept7/9b/11

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20554

7 January 2021

based on heuristic

inferred from DOI database lookup

Cytoskeletal modification of Rho guanine nucleotide exchange factor activity: identification of a Rho guanine nucleotide exchange factor as a binding partner for Sept9b, a mammalian septin

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20554

7 January 2021

based on heuristic

inferred from DOI database lookup

MSF (MLL septin-like fusion), a fusion partner gene of MLL, in a therapy-related acute myeloid leukemia with a t(11;17)(q23;q25)

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20554

7 January 2021

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Mapping of hereditary neuralgic amyotrophy (familial brachial plexus neuropathy) to distal chromosome 17q

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20554

7 January 2021

based on heuristic

inferred from DOI database lookup

Hereditary neuralgic amyotrophy: evidence for genetic homogeneity and mapping to chromosome 17q25

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20554

7 January 2021

based on heuristic

inferred from DOI database lookup

Here come the septins: novel polymers that coordinate intracellular functions and organization

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20554

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of a cell polarity-related protein, Lin-7B, as a binding partner for a Rho effector, Rhotekin, and their possible interaction in neurons

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20554

7 January 2021

based on heuristic

inferred from DOI database lookup

Complex networks orchestrate epithelial-mesenchymal transitions

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20554

7 January 2021

based on heuristic

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Evidence of a founder effect and refinement of the hereditary neuralgic amyotrophy (HNA) locus on 17q25 in American families

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20554

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/HUMU.20554

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

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