Characterization of SCML1, a new gene in Xp22, with homology to developmental polycomb genes (Q24312410)

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S M Walpole

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A Nicolaou

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P van der Bent

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A Cahn

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M Vaudin

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M T Ross

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J Durham

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R Pavitt

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J Wilkinson

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D Grafham

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A A Bergen

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G J van Ommen

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J R Yates

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J T den Dunnen

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D Trump

Regional localisation of a non-specific X-linked mental retardation gene (MRX19) to Xp22

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language of work or name

English

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publication date

1 April 1998

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published in

Genomics

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volume

49

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issue

1

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page(s)

96-102

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cites work

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https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

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

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7 January 2021

Severe congenital limb deficiencies, vertebral hypersegmentation, absent thymus and mirror polydactyly: a defect expression of a developmental control gene?

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7 January 2021

Fifteen dorsal vertebrae and rib pairs in two siblings

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7 January 2021

High-resolution mapping by YAC fragmentation of a 2.5-Mb Xp22 region containing the human RS, KFSD and CLS disease genes.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

Exclusion of PPEF as the gene causing X-linked juvenile retinoschisis.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

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https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

A 6-Mb YAC contig in Xp22.1-p22.2 spanning the DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3, and PHKA2 genes

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

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

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https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

Locking in stable states of gene expression: transcriptional control during Drosophila development.

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https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

Transformation of axial skeleton due to overexpression of bmi-1 in transgenic mice

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https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

Isolation of genes from complex sources of mammalian genomic DNA using exon amplification.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

Positional cloning of the gene associated with X-linked juvenile retinoschisis

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https://api.crossref.org/works/10.1006%2FGENO.1998.5224

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.1998.5224

7 January 2021

Deletions and translocations involving the distal short arm of the human X chromosome: review and hypotheses

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https://api.crossref.org/works/10.1006%2FGENO.1998.5224

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.1998.5224

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.1998.5224

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.1998.5224

7 January 2021

RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

An analysis of 5'-noncoding sequences from 699 vertebrate messenger RNAs

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

Scanning for genes in large genomic regions: cosmid-based exon trapping of multiple exons in a single product.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

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.1998.5224

7 January 2021

The polyhomeotic gene of Drosophila encodes a chromatin protein that shares polytene chromosome-binding sites with Polycomb

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

Posterior transformation, neurological abnormalities, and severe hematopoietic defects in mice with a targeted deletion of the bmi-1 proto-oncogene

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

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.1998.5224

7 January 2021

X linked retinoschisis

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

7 January 2021

Improved genetic mapping of X linked retinoschisis

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5224

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.1998.5224

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.1998.5224

7 January 2021