(Q40545350)

21 September 2017

Mapping of 262 DNA markers into 24 intervals on human chromosome 11. (English)

1 reference

21 September 2017

Tanigami A

1

1 reference

21 September 2017

Tokino T

2

1 reference

21 September 2017

Takiguchi S

3

1 reference

21 September 2017

Mori M

4

1 reference

21 September 2017

Glaser T

5

1 reference

21 September 2017

Park JW

6

1 reference

21 September 2017

Jones C

7

1 reference

21 September 2017

Nakamura Y

8

1 reference

21 September 2017

language of work or name

English

0 references

publication date

1 January 1992

1 reference

American Journal of Human Genetics

21 September 2017

1 reference

21 September 2017

50

1 reference

21 September 2017

56-64

1 reference

21 September 2017

1

1 reference

Comparison of constitutional and tumor-associated 11;22 translocations: nonidentical breakpoints on chromosomes 11 and 22

21 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682531

Chromosomal localization of the hst oncogene and its co-amplification with the int.2 oncogene in a human melanoma

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682531

Localization of an ataxia-telangiectasia gene to chromosome 11q22-23.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682531

Partial deletion of chromosome 11p in breast cancer correlates with size of primary tumour and oestrogen receptor level

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682531

Variable number of tandem repeat (VNTR) markers for human gene mapping

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682531

A fine-structure deletion map of human chromosome 11p: analysis of J1 series hybrids

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682531

Localization of the genetic defect in multiple endocrine neoplasia type 1 within a small region of chromosome 11.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682531

Genetic linkage of Beckwith-Wiedemann syndrome to 11p15.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682531

Analysis of human chromosome 21: correlation of physical and cytogenetic maps; gene and CpG island distributions

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682531

Exon trapping: a genetic screen to identify candidate transcribed sequences in cloned mammalian genomic DNA.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682531

Association within a family of a balanced autosomal translocation with major mental illness

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682531

Isolation and mapping of 62 new RFLP markers on human chromosome 11.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682531

Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682531

Co-amplification of integrated hepatitis B virus DNA and transforming gene hst-1 in a hepatocellular carcinoma

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682531

Mapping of a gene determining tuberous sclerosis to human chromosome 11q14-11q23.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682531

Allelic losses of chromosomes 9, 11, and 17 in human bladder cancer.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682531

Amplification of the int-2 gene in human head and neck squamous cell carcinomas

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682531

Isolation and mapping of 75 new DNA markers on human chromosome 3.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682531

Allelotype study of primary hepatocellular carcinoma

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682531

Loss of a c-H-ras-1 allele and aggressive human primary breast carcinomas

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682531

Numerical chromosome 1, 7, 9, and 11 aberrations in bladder cancer detected by in situ hybridization

4 November 2018

1 reference

12 December 2020

Amplification of human int-2 in breast cancers and squamous carcinomas

1 reference

12 December 2020

Loss of genes on the short arm of chromosome 11 in bladder cancer

1 reference

12 December 2020

Chromosomal localization of the human rhabdomyosarcoma locus by mitotic recombination mapping

1 reference

12 December 2020

Allelic loss on chromosome 11 in hereditary and sporadic tumors related to familial multiple endocrine neoplasia type 1

1 reference

12 December 2020

Clustering of breakpoints on chromosome 11 in human B-cell neoplasms with the t(11 ; 14) chromosome translocation

1 reference

12 December 2020

High incidence of coamplification of hst-1 and int-2 genes in human esophageal carcinomas

1 reference

12 December 2020

Deletions in human chromosome arms 11p and 13q in primary hepatocellular carcinomas

1 reference

12 December 2020

Reduction to homozygosity of genes on chromosome 11 in human breast neoplasia

1 reference

12 December 2020

Restriction sites containing CpG show a higher frequency of polymorphism in human DNA

1 reference

12 December 2020

Identifiers

1 reference

21 September 2017

1 reference