(Q21261242)

18 August 2022

Paola E Leone

1

Paola E

Leone

1 reference

18 August 2022

Marta Mendiola

series ordinal

2

author given names

Marta

author last names

Mendiola

1 reference

18 August 2022

César Paz-y-Miño

series ordinal

4

author given names

César

author last names

Paz-y-Miño

1 reference

18 August 2022

Angel Pestaña

series ordinal

5

author given names

Angel

author last names

Pestaña

1 reference

Gros1, a potential growth suppressor on chromosome 1: its identity to basement membrane-associated proteoglycan, leprecan

18 August 2022

language of work or name

English

0 references

publication date

4 March 2003

0 references

published in

BMC Cancer

0 references

volume

3

0 references

issue

1

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page(s)

6

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cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=152652

Human and mouse homologs of the Saccharomyces cerevisiae RAD54 DNA repair gene: evidence for functional conservation

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=152652

Cloning and sequencing a human homolog (hMYH) of the Escherichia coli mutY gene whose function is required for the repair of oxidative DNA damage

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=152652

Muf1, a novel Elongin BC-interacting leucine-rich repeat protein that can assemble with Cul5 and Rbx1 to reconstitute a ubiquitin ligase

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=152652

Mutations in the RAD54 recombination gene in primary cancers

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=152652

Structure of the gene encoding the human cyclin-dependent kinase inhibitor p18 and mutational analysis in breast cancer

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=152652

Characterization of the human homologue of RAD54: a gene located on chromosome 1p32 at a region of high loss of heterozygosity in breast tumors

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=152652

A short primer on RNAi: RNA-directed RNA polymerase acts as a key catalyst

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=152652

Gene silencing by double-stranded RNA.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=152652

Isolation and characterization of human patched 2 (PTCH2), a putative tumour suppressor gene inbasal cell carcinoma and medulloblastoma on chromosome 1p32.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=152652

An scl gene product lacking the transactivation domain induces bony abnormalities and cooperates with LMO1 to generate T-cell malignancies in transgenic mice

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=152652

Molecular cloning and chromosomal localization of the murine homolog of the human helix-loop-helix gene SCL

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=152652

Epidemiology and etiology of intracranial meningiomas: a review

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=152652

Molecular genetic investigation of the neurofibromatosis type 2 tumor suppressor gene in sporadic meningioma.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=152652

NF2 gene mutations and allelic status of 1p, 14q and 22q in sporadic meningiomas.

27 September 2017

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1471-2407-3-6

Chromosomal deletions in anaplastic meningiomas suggest multiple regions outside chromosome 22 as important in tumor progression.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1471-2407-3-6

Incidence and clinical features of asymptomatic meningiomas

21 January 2018

1 reference

12 December 2020

Frequent loss of 1p32 region but no mutation of the p18 tumor suppressor gene in meningiomas

1 reference

12 December 2020

1p and 3p deletions in meningiomas without detectable aberrations of chromosome 22 identified by comparative genomic hybridization

1 reference

12 December 2020

Identification of a consistent region of allelic loss on 1p32 in meningiomas: correlation with increased morbidity

1 reference

12 December 2020

Search for mutations of the hRAD54 gene in sporadic meningiomas with deletion at 1p32

1 reference

12 December 2020

Allelic losses in neurofibromatosis 2-associated meningiomas

1 reference

12 December 2020

Identifiers

DOI

10.1186/1471-2407-3-6

0 references