Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 RanBP1, a velocardiofacial/DiGeorge syndrome candidate gene, is expressed at sites of mesenchymal/epithelial induction.

Literature DB >> 11804793

RanBP1, a velocardiofacial/DiGeorge syndrome candidate gene, is expressed at sites of mesenchymal/epithelial induction.

Thomas M Maynard¹, Gloria T Haskell, Naina Bhasin, James M Lee, Andrew A Gassman, Jeffrey A Lieberman, Anthony-Samuel LaMantia.

Abstract

RanBP1, a velocardiofacial syndrome/DiGeorge syndrome candidate gene, is expressed in the frontonasal processes, branchial arches, aortic arches, and limb buds. At these sites, RanBP1 apparently coincides with neural crest-derived mesenchymal cells. In addition, RanBP1 is expressed in the forebrain as well as in hindbrain regions previously associated with crest-derived mesenchymal cells.

Entities: Disease Gene

Mesh：

Substances：

Year: 2002 PMID： 11804793 DOI： 10.1016/s0925-4773(01)00616-5

Source DB: PubMed Journal: Mech Dev ISSN： 0925-4773 Impact factor: 1.882

Keyword Cloud
Cited

12 in total

Review 1. The molecular pathology of primary immunodeficiencies.

Authors: Megan S Lim; Kojo S J Elenitoba-Johnson
Journal: J Mol Diagn Date: 2004-05 Impact factor: 5.568

2. No evidence for parental imprinting of mouse 22q11 gene orthologs.

Authors: Thomas M Maynard; Daniel W Meechan; Clifford C Heindel; Amanda Z Peters; Robert M Hamer; Jeffrey A Lieberman; Anthony-Samuel LaMantia
Journal: Mamm Genome Date: 2006-08-04 Impact factor: 2.957

3. Ranbp1, Deleted in DiGeorge/22q11.2 Deletion Syndrome, is a Microcephaly Gene That Selectively Disrupts Layer 2/3 Cortical Projection Neuron Generation.

Authors: Elizabeth M Paronett; Daniel W Meechan; Beverly A Karpinski; Anthony-Samuel LaMantia; Thomas M Maynard
Journal: Cereb Cortex Date: 2014-12-01 Impact factor: 5.357

Review 4. Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit development.

Authors: Daniel W Meechan; Thomas M Maynard; Eric S Tucker; Alejandra Fernandez; Beverly A Karpinski; Lawrence A Rothblat; Anthony-S LaMantia
Journal: Prog Neurobiol Date: 2015-04-09 Impact factor: 11.685

Review 5. Three phases of DiGeorge/22q11 deletion syndrome pathogenesis during brain development: patterning, proliferation, and mitochondrial functions of 22q11 genes.

Authors: D W Meechan; T M Maynard; E S Tucker; A-S LaMantia
Journal: Int J Dev Neurosci Date: 2010-09-15 Impact factor: 2.457

RanBP1, a velocardiofacial/DiGeorge syndrome candidate gene, is expressed at sites of mesenchymal/epithelial induction.

Review 1. The molecular pathology of primary immunodeficiencies.

2. No evidence for parental imprinting of mouse 22q11 gene orthologs.

3. Ranbp1, Deleted in DiGeorge/22q11.2 Deletion Syndrome, is a Microcephaly Gene That Selectively Disrupts Layer 2/3 Cortical Projection Neuron Generation.

Review 4. Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit development.

Review 5. Three phases of DiGeorge/22q11 deletion syndrome pathogenesis during brain development: patterning, proliferation, and mitochondrial functions of 22q11 genes.

Review 6. When half is not enough: gene expression and dosage in the 22q11 deletion syndrome.

7. A comprehensive analysis of 22q11 gene expression in the developing and adult brain.

Review 8. Hard to swallow: Developmental biological insights into pediatric dysphagia.

9. Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome.

Review 10. In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects?