(Q34581812)

3 August 2017

title

Crim1KST264/KST264 mice display a disruption of the Crim1 gene resulting in perinatal lethality with defects in multiple organ systems (English)

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3 August 2017

1

David J Pennisi

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3 August 2017

Kevin Gillinder

5

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Lorine J Wilkinson

object named as

Lorine Wilkinson

2

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Melissa Little

object named as

Melissa H Little

9

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Michael Piper

object named as

Michael J Piper

6

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author name string

Gabriel Kolle

3

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3 August 2017

Michael L Sohaskey

4

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3 August 2017

John W McAvoy

7

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3 August 2017

Frank J Lovicu

8

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3 August 2017

publication date

1 February 2007

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3 August 2017

published in

Developmental Dynamics

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3 August 2017

volume

236

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3 August 2017

issue

2

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3 August 2017

page(s)

502-511

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Contributions by members of the TGFbeta superfamily to lens development

3 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21015

7 January 2021

Histochemical staining following LacZ gene transfer underestimates transfection efficiency.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21015

7 January 2021

α3β1 Integrin Is Required for Normal Development of the Epidermal Basement Membrane

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21015

7 January 2021

A requirement for bone morphogenetic protein-7 during development of the mammalian kidney and eye

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21015

7 January 2021

Chordin-like CR domains and the regulation of evolutionarily conserved extracellular signaling systems.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21015

7 January 2021

Characterisation of Crim1 expression in the developing mouse urogenital tract reveals a sexually dimorphic gonadal expression pattern

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21015

7 January 2021

Absence of integrin alpha 6 leads to epidermolysis bullosa and neonatal death in mice.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21015

7 January 2021

CRIM1 is involved in endothelial cell capillary formation in vitro and is expressed in blood vessels in vivo

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21015

7 January 2021

Identification of a new gene mutated in Fraser syndrome and mouse myelencephalic blebs

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21015

7 January 2021

BMP7 null mutation in mice: developmental defects in skeleton, kidney, and eye.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21015

7 January 2021

BMP 7 is required for nephrogenesis, eye development, and skeletal patterning

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21015

7 January 2021

Knockdown of zebrafish crim1 results in a bent tail phenotype with defects in somite and vascular development

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21015

7 January 2021

CRIM1, a novel gene encoding a cysteine-rich repeat protein, is developmentally regulated and implicated in vertebrate CNS development and organogenesis

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21015

7 January 2021

Defining brain wiring patterns and mechanisms through gene trapping in mice.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21015

7 January 2021

Expression of Crim1 during murine ocular development.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21015

7 January 2021

BMP-7 is an inducer of nephrogenesis, and is also required for eye development and skeletal patterning

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21015

7 January 2021

Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21015

7 January 2021

Roles for laminin in embryogenesis: exencephaly, syndactyly, and placentopathy in mice lacking the laminin alpha5 chain

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21015

7 January 2021

Mice null for sox18 are viable and display a mild coat defect

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21015

7 January 2021

Conditional ablation of beta1 integrin in skin. Severe defects in epidermal proliferation, basement membrane formation, and hair follicle invagination

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21015

7 January 2021

Capturing genes encoding membrane and secreted proteins important for mouse development

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21015

7 January 2021

The genetics of Fraser syndrome and the blebs mouse mutants

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21015

7 January 2021

The extracellular matrix gene Frem1 is essential for the normal adhesion of the embryonic epidermis

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21015

7 January 2021

A direct functional link between the multi-PDZ domain protein GRIP1 and the Fraser syndrome protein Fras1

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21015

7 January 2021

Integrin beta 4 mutations associated with junctional epidermolysis bullosa with pyloric atresia

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21015

7 January 2021

Fras1 deficiency results in cryptophthalmos, renal agenesis and blebbed phenotype in mice

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21015

7 January 2021

CRIM1 regulates the rate of processing and delivery of bone morphogenetic proteins to the cell surface.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21015

7 January 2021

Identifiers

DOI

10.1002/DVDY.21015

1 reference

3 August 2017

1 reference