(Q24316979)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9119407%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

title

SMT3A, a human homologue of the S. cerevisiae SMT3 gene, maps to chromosome 21qter and defines a novel gene family (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9119407%20AND%20SRC:MED&resulttype=core&format=json

Small ubiquitin like modifier 3

2 November 2019

main subject

1 reference

GOA release 2020-03-11

author

Antonio Pizzuti

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9119407%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

author name string

Lapenta V

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9119407%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

Chiurazzi P

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9119407%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

van der Spek P

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9119407%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

Hanaoka F

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9119407%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

Brahe C

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9119407%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

language of work or name

English

0 references

publication date

1 March 1997

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9119407%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9119407%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

volume

40

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9119407%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

page(s)

362-366

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9119407%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9119407%20AND%20SRC:MED&resulttype=core&format=json

A compositional map of human chromosome 21.

2 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1996.4556

7 January 2021

Human elongation factor EF-1 beta: cloning and characterization of the EF1 beta 5a gene and assignment of EF-1 beta isoforms to chromosomes 2,5,15 and X

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1996.4556

7 January 2021

Cloning and expression of human homolog HSMT3 to yeast SMT3 suppressor of MIF2 mutations in a centromere protein gene

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1996.4556

7 January 2021

An integrated map with cosmid/PAC contigs of a 4-Mb Down syndrome critical region

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1996.4556

7 January 2021

UBL1, a human ubiquitin-like protein associating with human RAD51/RAD52 proteins

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1996.4556

7 January 2021

Isolation of two genes that affect mitotic chromosome transmission in S. cerevisiae.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1996.4556

7 January 2021

Cosmid assembly and anchoring to human chromosome 21.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1996.4556

7 January 2021

An autosomal locus causing autoimmune disease: autoimmune polyglandular disease type I assigned to chromosome 21

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1996.4556

7 January 2021

Type VI collagen mutations in Bethlem myopathy, an autosomal dominant myopathy with contractures

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1996.4556

7 January 2021

A possible vulnerability locus for bipolar affective disorder on chromosome 21q22.3.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1996.4556

7 January 2021

Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1996.4556

7 January 2021

cDNA selection: efficient PCR approach for the selection of cDNAs encoded in large chromosomal DNA fragments

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1996.4556

7 January 2021

Exon amplification: a strategy to isolate mammalian genes based on RNA splicing

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1996.4556

7 January 2021

Down syndrome phenotypes: the consequences of chromosomal imbalance

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1996.4556

7 January 2021

Construction and characterization of a normalized cDNA library

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1996.4556

7 January 2021

MIF2 is required for mitotic spindle integrity during anaphase spindle elongation in Saccharomyces cerevisiae

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1996.4556

7 January 2021

CENP-C is required for maintaining proper kinetochore size and for a timely transition to anaphase.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1996.4556

7 January 2021

Yeast ubiquitin-like genes are involved in duplication of the microtubule organizing center

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1996.4556

7 January 2021

Evidence that the MIF2 gene of Saccharomyces cerevisiae encodes a centromere protein with homology to the mammalian centromere protein CENP-C

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1996.4556

7 January 2021

Domains required for CENP-C assembly at the kinetochore

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1996.4556

7 January 2021

Identification of genes using oligonucleotides corresponding to splice site consensus sequences

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1996.4556

7 January 2021

An integrated YAC-overlap and 'cosmid-pocket' map of the human chromosome 21.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1996.4556

7 January 2021

A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1996.4556

7 January 2021

Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1)

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1996.4556

7 January 2021

Molecular mapping of twenty-four features of Down syndrome on chromosome 21.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1996.4556

7 January 2021