(Q30501651)

21 September 2017

Equal parental origin of chromosome 22 losses in human sporadic meningioma: no evidence for genomic imprinting (English)

1 reference

21 September 2017

7

J F Gusella

1 reference

21 September 2017

2

G A Rouleau

1 reference

21 September 2017

B Fontaine

1

1 reference

21 September 2017

B Seizinger

3

1 reference

21 September 2017

A F Jewell

4

1 reference

21 September 2017

M P Hanson

5

1 reference

21 September 2017

R L Martuza

6

1 reference

21 September 2017

language of work or name

English

0 references

publication date

1 November 1990

1 reference

American Journal of Human Genetics

21 September 2017

1 reference

21 September 2017

47

1 reference

21 September 2017

5

1 reference

21 September 2017

823-827

1 reference

A polymorphic DNA marker genetically linked to Huntington's disease

21 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683679

Neurofibromatosis 2 (bilateral acoustic neurofibromatosis).

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683679

Molecular genetic approach to human meningioma: loss of genes on chromosome 22

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683679

Hereditary cancer, oncogenes, and antioncogenes.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683679

Preferential mutation of paternally derived RB gene as the initial event in sporadic osteosarcoma.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683679

Deletion mapping of a locus on human chromosome 22 involved in the oncogenesis of meningioma

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683679

Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683679

A model for embryonal rhabdomyosarcoma tumorigenesis that involves genome imprinting

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683679

Genomic imprinting and genetic disorders in man.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683679

Report of the committee on the genetic constitution of chromosome 22.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683679

Oncogenes, antioncogenes, and the molecular bases of multistep carcinogenesis

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683679

Unequal parental contributions: genomic imprinting in mammals.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683679

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683679

Paternal origin of new mutations in von Recklinghausen neurofibromatosis.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683679

Chromosome translocation t(14;22) and oncogene (c-sis) variant in a pedigree with familial meningioma

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683679

Genomic imprinting determines methylation of parental alleles in transgenic mice

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683679

Preferential germline mutation of the paternal allele in retinoblastoma

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683679

Allele-specific methylation of the human c-Ha-ras-1 gene

26 November 2018

1 reference

12 December 2020

Parental legacy determines methylation and expression of an autosomal transgene: a molecular mechanism for parental imprinting

1 reference

12 December 2020

Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22

1 reference

12 December 2020

Maternal inhibition of hepatitis B surface antigen gene expression in transgenic mice correlates with de novo methylation.

1 reference

12 December 2020

Gene losses in human tumours

1 reference

12 December 2020

Genomic imprinting and embryonal tumours

1 reference

12 December 2020

Point mutational inactivation of the retinoblastoma antioncogene

1 reference

12 December 2020

Parental origin of mutations of the retinoblastoma gene

1 reference

12 December 2020

Identifiers

1 reference

21 September 2017

PubMed publication ID

2220822

1 reference