(Q28505391)

24 January 2017

title

Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome (English)

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V-crk avian sarcoma virus CT10 oncogene homolog-like

24 January 2017

main subject

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GOA release 2020-03-11

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D. L. Guris

1

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24 January 2017

J. Fantes

2

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24 January 2017

D. Tara

3

1 reference

24 January 2017

B. J. Druker

4

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24 January 2017

A. Imamoto

5

1 reference

24 January 2017

language of work or name

English

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publication date

1 March 2001

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24 January 2017

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24 January 2017

volume

27

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24 January 2017

issue

3

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24 January 2017

page(s)

293–298

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The DNA sequence of human chromosome 22

24 January 2017

cites work

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7 January 2021

Induction and patterning of the neural crest, a stem cell-like precursor population

1 reference

7 January 2021

Physiological signals and oncogenesis mediated through Crk family adapter proteins

1 reference

7 January 2021

Role of the adapter protein CRKL in signal transduction of normal hematopoietic and BCR/ABL-transformed cells

1 reference

7 January 2021

Contributions of placodal and neural crest cells to avian cranial peripheral ganglia

1 reference

7 January 2021

Development of the peripheral nervous system from the neural crest

1 reference

7 January 2021

Glial growth factor restricts mammalian neural crest stem cells to a glial fate

1 reference

7 January 2021

Neu differentiation factor is a neuron-glia signal and regulates survival, proliferation, and maturation of rat Schwann cell precursors.

1 reference

7 January 2021

Isolation of a stem cell for neurons and glia from the mammalian neural crest

1 reference

7 January 2021

Cardiac neural crest is essential for the persistence rather than the formation of an arch artery

1 reference

7 January 2021

A common molecular basis for rearrangement disorders on chromosome 22q11

1 reference

7 January 2021

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

1 reference

7 January 2021

Detection of a 22q11.2 deletion in cardiac patients suggests a risk for velopharyngeal incompetence

1 reference

7 January 2021

Dysphagia in children with a 22q11.2 deletion: unusual pattern found on modified barium swallow

1 reference

7 January 2021

Deletion of 150 kb in the minimal DiGeorge/velocardiofacial syndrome critical region in mouse.

1 reference

7 January 2021

Mutations in the human TWIST gene

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7 January 2021

twist is required in head mesenchyme for cranial neural tube morphogenesis

1 reference

7 January 2021

GATA3 haplo-insufficiency causes human HDR syndrome

1 reference

7 January 2021

Another critical region for deletion of 22q11: a study of 100 patients.

1 reference

7 January 2021

Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndrome

1 reference

7 January 2021

A revision of the lissencephaly and Miller-Dieker syndrome critical regions in chromosome 17p13.3.

1 reference

7 January 2021

A novel role for cardiac neural crest in heart development

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7 January 2021

Development of a lethal congenital heart defect in the splotch (Pax3) mutant mouse.

1 reference

7 January 2021