Identification of SCML2, a second human gene homologous to the Drosophila sex comb on midleg (Scm): A new gene cluster on Xp22 (Q22010050)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10331946%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

title

Identification of SCML2, a second human gene homologous to the Drosophila sex comb on midleg (Scm): A new gene cluster on Xp22 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10331946%20AND%20SRC:MED&resulttype=core&format=json

Scm polycomb group protein like 2

8 December 2019

main subject

Drosophila

0 references

1 reference

anatomical structure morphogenesis

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

1

E Montini

E

Montini

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10331946%20AND%20SRC:MED&resulttype=core&format=json

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9

A Ballabio

A

Ballabio

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10331946%20AND%20SRC:MED&resulttype=core&format=json

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10

B Franco

B

Franco

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10331946%20AND%20SRC:MED&resulttype=core&format=json

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G Buchner

2

G

Buchner

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C Spalluto

3

C

Spalluto

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G Andolfi

4

G

Andolfi

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10331946%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

A Caruso

5

A

Caruso

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8 December 2019

J T den Dunnen

6

J T

den Dunnen

1 reference

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8 December 2019

D Trump

7

D

Trump

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M Rocchi

8

M

Rocchi

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8 December 2019

language of work or name

English

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publication date

1 May 1999

1 reference

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8 December 2019

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8 December 2019

volume

58

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8 December 2019

page(s)

65-72

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8 December 2019

issue

1

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8 December 2019

cites work

XLMR genes: update 1996.

1 reference

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7 January 2021

Nance-Horan syndrome: linkage analysis in a family from The Netherlands

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7 January 2021

High-resolution physical map of the X-linked retinoschisis interval in Xp22.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5755

7 January 2021

Characterization of SCML1, a new gene in Xp22, with homology to developmental polycomb genes

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5755

7 January 2021

Identification and characterization of a novel serine-threonine kinase gene from the Xp22 region

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5755

7 January 2021

Functional analysis of mouse Polycomb group genes

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7 January 2021

Nance-Horan syndrome: linkage analysis in 4 families refines localization in Xp22.31-p22.13 region.

1 reference

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7 January 2021

The complex genetic locus polyhomeotic in Drosophila melanogaster potentially encodes two homologous zinc-finger proteins

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5755

7 January 2021

The Drosophila melanogaster tumor suppressor gene lethal(3)malignant brain tumor encodes a proline-rich protein with a novel zinc finger.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5755

7 January 2021

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7 January 2021

Murine Polycomb- and trithorax-group genes regulate homeotic pathways and beyond.

1 reference

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7 January 2021

Chromatin-silencing mechanisms in Drosophila maintain patterns of gene expression

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7 January 2021

PcG complexes and chromatin silencing

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5755

7 January 2021

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5755

7 January 2021

Cloning of PBDX, an MIC2-related gene that spans the pseudoautosomal boundary on chromosome Xp.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5755

7 January 2021

Expression pattern of the Kallmann syndrome gene in the olfactory system suggests a role in neuronal targeting.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5755

7 January 2021

Identification and mapping of human cDNAs homologous to Drosophila mutant genes through EST database searching.

1 reference

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7 January 2021

PBDX is the XG blood group gene

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5755

7 January 2021

MEHMO (mental retardation, epileptic seizures, hypogonadism and -genitalism, microcephaly, obesity), a novel syndrome: assignment of disease locus to xp21.1-p22.13.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5755

7 January 2021

MIC2R: a transcribed MIC2-related sequence associated with a CpG island in the human pseudoautosomal region

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5755

7 January 2021

An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3–Xp21.3

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5755

7 January 2021

Characterization of a cluster of sulfatase genes on Xp22.3 suggests gene duplications in an ancestral pseudoautosomal region

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5755

7 January 2021

A novel locus for non-syndromic sensorineural deafness (DFN6) maps to chromosome Xp22.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5755

7 January 2021

A novel human serine-threonine phosphatase related to the Drosophila retinal degeneration C (rdgC) gene is selectively expressed in sensory neurons of neural crest origin

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5755

7 January 2021

The oral-facial-digital syndrome type 1 (OFD1), a cause of polycystic kidney disease and associated malformations, maps to Xp22.2-Xp22.3.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5755

7 January 2021

Compilation and analysis of sequences upstream from the translational start site in eukaryotic mRNAs

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5755

7 January 2021

Identification of Bmi1-interacting proteins as constituents of a multimeric mammalian polycomb complex

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5755

7 January 2021

High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5755

7 January 2021

Identification and characterization of interactions between the vertebrate polycomb-group protein BMI1 and human homologs of polyhomeotic

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5755

7 January 2021

Fried syndrome is a distinct X linked mental retardation syndrome mapping to Xp22.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5755

7 January 2021

An Xp22.1-p22.2 YAC contig encompassing the disease loci for RS, KFSD, CLS, HYP and RP15: refined localization of RS

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5755

7 January 2021

Identifiers

DOI

10.1006/GENO.1999.5755

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10331946%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

1 reference