22q11 DS: genomic mechanisms and gene function in DiGeorge/velocardiofacial syndrome-Reference-Cited by-同舟云学术

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22q11 DS: genomic mechanisms and gene function in DiGeorge/velocardiofacial syndrome

Published:2002-05-16 Issue:3-5 Volume:20 Page:407-419
ISSN:0736-5748
Container-title:International Journal of Developmental Neuroscience
language:en
Short-container-title:Int. j. dev. neurosci.

Author:

Maynard Thomas M.¹²,Haskell Gloria T.¹³,Lieberman Jeffrey A.⁴,LaMantia Anthony‐Samuel¹³

Affiliation:

1. Department of Cell and Molecular Physiology, CB #7545UNC School of MedicineUniversity of North CarolinaChapel HillNC27599USA

2. UNC Neurodevelopmental Disorders Research CenterUNC School of MedicineUniversity of North CarolinaChapel HillNC27599USA

3. UNC Neuroscience CenterUNC School of MedicineUniversity of North CarolinaChapel HillNC27599USA

4. Department of PsychiatryUNC School of MedicineUniversity of North CarolinaChapel HillNC27599USA

Funder

National Alliance for Research on Schizophrenia and Depression

Publisher

Wiley

Subject

Developmental Biology,Developmental Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1016/S0736-5748%2802%2900050-3

Reference120 articles.

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

2. Isolation of a zinc finger gene consistently deleted in DiGeorge syndrome

3. 22q11 deletion syndrome: a genetic subtype of schizophrenia

4. The septin CDCrel-1 binds syntaxin and inhibits exocytosis

5. Cloning and characterization of the gene encoding human NPL4, a protein interacting with the ubiquitin fusion-degradation protein (UFD1L)

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1. Synaptic Plasticity Dysfunctions in the Pathophysiology of 22q11 Deletion Syndrome: Is There a Role for Astrocytes?;International Journal of Molecular Sciences;2022-04-16

2. A Link between Genetic Disorders and Cellular Impairment, Using Human Induced Pluripotent Stem Cells to Reveal the Functional Consequences of Copy Number Variations in the Central Nervous System—A Close Look at Chromosome 15;International Journal of Molecular Sciences;2020-03-09

3. Participatory development of a patient–clinician communication tool to enhance healthcare transitions for young people with 22q11.2;Irish Journal of Medical Science (1971 -);2019-12-04

4. The strengths of the genetic approach to understanding neural systems development and function: Ray Guillery's synthesis;European Journal of Neuroscience;2018-08

5. Distinct white-matter aberrations in 22q11.2 deletion syndrome and patients at ultra-high risk for psychosis;Psychological Medicine;2016-05-19

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