(Q24291727)

NPL4 homolog, ubiquitin recognition factor

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author name string

A Botta

1

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C Tandoi

2

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G Fini

3

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G Calabrese

4

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B Dallapiccola

5

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G Novelli

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

6

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language of work or name

English

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publication date

5 September 2001

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published in

Gene

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volume

275

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issue

1

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page(s)

39-46

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cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900649-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900649-7

7 January 2021

Chromosome mapping of the human arrestin (SAG), beta-arrestin 2 (ARRB2), and beta-adrenergic receptor kinase 2 (ADRBK2) genes

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900649-7

7 January 2021

Nuclear transport defects and nuclear envelope alterations are associated with mutation of the Saccharomyces cerevisiae NPL4 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900649-7

7 January 2021

The Uba2 and Ufd1 proteins of Saccharomyces cerevisiae interact with poly(A) polymerase and affect the polyadenylation activity of cell extracts

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900649-7

7 January 2021

The DNA sequence of human chromosome 22

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900649-7

7 January 2021

A novel genetic system to detect protein-protein interactions

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900649-7

7 January 2021

DiGeorge syndrome: an historical review of clinical and cytogenetic features

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900649-7

7 January 2021

DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900649-7

7 January 2021

A proteolytic pathway that recognizes ubiquitin as a degradation signal

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900649-7

7 January 2021

Role of neural crest in congenital heart disease

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900649-7

7 January 2021

Congenital heart disease in mice deficient for the DiGeorge syndrome region

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900649-7

7 January 2021

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900649-7

7 January 2021

Patient with a 22q11.2 deletion with no overlap of the minimal DiGeorge syndrome critical region (MDGCR).

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900649-7

7 January 2021

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900649-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900649-7

7 January 2021

Nup153 is an M9-containing mobile nucleoporin with a novel Ran-binding domain

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900649-7

7 January 2021

UFD1L and CDC45L: a role in DiGeorge syndrome and related phenotypes?

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900649-7

7 January 2021

Detection of an atypical 22q11 deletion that has no overlap with the DiGeorge syndrome critical region

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900649-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900649-7

7 January 2021

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900649-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900649-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900649-7

7 January 2021

GTP hydrolysis links initiation and termination of nuclear import on the nucleoporin nup358

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2801%2900649-7

7 January 2021