(Q40787272)

23 September 2017

title

Association study of a promoter polymorphism of UFD1L gene with schizophrenia (English)

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23 September 2017

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10

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11

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12

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De Luca A

1

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Pasini A

2

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Amati F

3

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Botta A

4

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Spalletta G

5

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23 September 2017

Alimenti S

6

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23 September 2017

Caccamo F

7

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Conti E

8

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Trakalo J

9

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23 September 2017

publication date

1 August 2001

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American Journal of Medical Genetics Part A

23 September 2017

published in

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23 September 2017

volume

105

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23 September 2017

issue

6

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23 September 2017

page(s)

529-533

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22q11 deletion syndrome: a genetic subtype of schizophrenia

23 September 2017

cites work

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The gene encoding proline dehydrogenase modulates sensorimotor gating in mice

21 January 2018

1 reference

A proteolytic pathway that recognizes ubiquitin as a degradation signal

21 January 2018

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Programmed cell death: implications for neuropsychiatric disorders

21 January 2018

1 reference

A complex of mammalian ufd1 and npl4 links the AAA-ATPase, p97, to ubiquitin and nuclear transport pathways

21 January 2018

1 reference

Defects in the ubiquitin pathway induce caspase-independent apoptosis blocked by Bcl-2.

21 January 2018

1 reference

Structure and expression of the human ubiquitin fusion-degradation gene (UFD1L).

21 January 2018

1 reference

Candidate-gene association studies of schizophrenia

21 January 2018

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UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome

21 January 2018

1 reference

Linkage and associated studies of schizophrenia

21 January 2018

1 reference

The HPV-16 E6 and E6-AP complex functions as a ubiquitin-protein ligase in the ubiquitination of p53

21 January 2018

1 reference

A sibship test for linkage in the presence of association: the sib transmission/disequilibrium test

21 January 2018

1 reference

Velocardiofacial syndrome in childhood-onset schizophrenia.

21 January 2018

1 reference

Mutations of UFD1L are not responsible for the majority of cases of DiGeorge Syndrome/velocardiofacial syndrome without deletions within chromosome 22q11.

21 January 2018

1 reference

A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects

21 January 2018

1 reference

NF-κB p105 Processing via the Ubiquitin-Proteasome Pathway

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/AJMG.1489

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23 September 2017

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