(Q52061727)

20 April 2018

title

Evidence of functional redundancy between MID proteins: implications for the presentation of Opitz syndrome. (English)

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20 April 2018

author name string

Alessandra Granata

1

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20 April 2018

Dawn Savery

2

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20 April 2018

Jamile Hazan

3

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20 April 2018

Billy M F Cheung

4

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20 April 2018

Andrew Lumsden

5

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20 April 2018

Nandita A Quaderi

6

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20 April 2018

language of work or name

English

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publication date

1 January 2005

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20 April 2018

number of pages

8

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based on heuristic

inferred from page(s)

published in

Developmental Biology

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20 April 2018

volume

277

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20 April 2018

issue

2

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20 April 2018

page(s)

417-424

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20 April 2018

FGF8 functions in the specification of the right body side of the chick

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

MID2, a homologue of the Opitz syndrome gene MID1: similarities in subcellular localization and differences in expression during development

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

Functional characterization of the Opitz syndrome gene product (midin): evidence for homodimerization and association with microtubules throughout the cell cycle

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

Mechanisms of left-right determination in vertebrates

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

Improved method for chick whole-embryo culture using a filter paper carrier

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

Role of notochord in specification of cardiac left-right orientation in zebrafish and Xenopus

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

X-linked Opitz syndrome: novel mutations in the MID1 gene and redefinition of the clinical spectrum

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

FGF8 acts as a right determinant during establishment of the left-right axis in the rabbit.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

Opitz G/BBB syndrome in Xp22: mutations in the MID1 gene cluster in the carboxy-terminal domain

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

The Opitz syndrome gene MID1 is essential for establishing asymmetric gene expression in Hensen's node

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

A series of normal stages in the development of the chick embryo

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

RING finger proteins: mediators of ubiquitin ligase activity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

Human homolog of patched, a candidate gene for the basal cell nevus syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

Motor protein control of ion flux is an early step in embryonic left–right asymmetry

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

A molecular pathway determining left-right asymmetry in chick embryogenesis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

Phosphorylation and microtubule association of the Opitz syndrome protein mid-1 is regulated by protein phosphatase 2A via binding to the regulatory subunit alpha 4.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

Left-right asymmetry determination in vertebrates

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

Differences in left-right axis pathways in mouse and chick: functions of FGF8 and SHH

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

FXY2/MID2, a gene related to the X-linked Opitz syndrome gene FXY/MID1, maps to Xq22 and encodes a FNIII domain-containing protein that associates with microtubules.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

The tripartite motif family identifies cell compartments

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

Midline and laterality defects: left and right meet in the middle

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

The Opitz syndrome gene product, MID1, associates with microtubules

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

Churchill, a zinc finger transcriptional activator, regulates the transition between gastrulation and neurulation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

MID1 and MID2 homo- and heterodimerise to tether the rapamycin-sensitive PP2A regulatory subunit, alpha 4, to microtubules: implications for the clinical variability of X-linked Opitz GBBB syndrome and other developmental disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

MID1, mutated in Opitz syndrome, encodes an ubiquitin ligase that targets phosphatase 2A for degradation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.036

10.1016/J.YDBIO.2004.09.036

7 January 2021

Identifiers

DOI

1 reference

20 April 2018

PubMed ID

15617684

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20 April 2018