(Q38335475)

English

Detection of allelic imbalance in the gene expression of hMSH2 or RB1 in lymphocytes from pedigrees of hereditary, nonpolyposis, colorectal cancer and retinoblastoma by an RNA difference plot

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scholarly article

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Europe PubMed Central

PubMed publication ID

2 September 2017

Detection of allelic imbalance in the gene expression of hMSH2 or RB1 in lymphocytes from pedigrees of hereditary, nonpolyposis, colorectal cancer and retinoblastoma by an RNA difference plot (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

colorectal cancer

1 reference

based on heuristic

inferred from title

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based on heuristic

inferred from title

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based on heuristic

inferred from title

Mika Sakurai-Yageta

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author name string

Yoshinori Murakami

1

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

Kana Isogai

2

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

Hiroyuki Tomita

3

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

Mika Sakurai-Yageta

4

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

Tomoko Maruyama

5

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

Akio Hidaka

6

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

Kiyoshi Nose

7

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Europe PubMed Central

PubMed publication ID

2 September 2017

Kokichi Sugano

8

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

Akihiro Kaneko

9

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Europe PubMed Central

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2 September 2017

publication date

8 October 2004

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Europe PubMed Central

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2 September 2017

Journal of Human Genetics

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Europe PubMed Central

PubMed publication ID

2 September 2017

49

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Europe PubMed Central

PubMed publication ID

2 September 2017

11

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Europe PubMed Central

PubMed publication ID

2 September 2017

635-641

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Europe PubMed Central

PubMed publication ID

2 September 2017

https://scigraph.springernature.com/pub.10.1007/s10038-004-0201-0

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Detection of aberrations of the p53 alleles and the gene transcript in human tumor cell lines by single-strand conformation polymorphism analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15480874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Small changes in expression affect predisposition to tumorigenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15480874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enhanced detection of deleterious and other germline mutations of hMSH2 and hMLH1 in Japanese hereditary nonpolyposis colorectal cancer kindreds

1 reference

https://pubmed.ncbi.nlm.nih.gov/15480874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reprogramming of genome function through epigenetic inheritance

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https://pubmed.ncbi.nlm.nih.gov/15480874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allelic Variation in Human Gene Expression

1 reference

https://pubmed.ncbi.nlm.nih.gov/15480874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15480874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Growth suppression by an E2F-binding-defective retinoblastoma protein (RB): contribution from the RB C pocket

1 reference

https://pubmed.ncbi.nlm.nih.gov/15480874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nonsense-mediated mRNA decay in health and disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/15480874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Temperature-sensitive RB mutations linked to incomplete penetrance of familial retinoblastoma in 12 families

1 reference

https://pubmed.ncbi.nlm.nih.gov/15480874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Ligase-Mediated Gene Detection Technique

1 reference

https://pubmed.ncbi.nlm.nih.gov/15480874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sensitive detection of loss of heterozygosity in the TP53 gene in pancreatic adenocarcinoma by fluorescence-based single-strand conformation polymorphism analysis using blunt-end DNA fragments

1 reference

https://pubmed.ncbi.nlm.nih.gov/15480874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/15480874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitative analysis of messenger RNA levels: reverse transcription-polymerase chain reaction single nucleotide primer extension assay

1 reference

https://pubmed.ncbi.nlm.nih.gov/15480874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Counting alleles reveals a connection between chromosome 18q loss and vascular invasion

1 reference

https://pubmed.ncbi.nlm.nih.gov/15480874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Outpatient clinic for genetic counseling and gene testing of retinoblastoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/15480874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hot-stop PCR: a simple and general assay for linear quantitation of allele ratios

1 reference

https://pubmed.ncbi.nlm.nih.gov/15480874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A variation in the structure of the protein-coding region of the human p53 gene.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15480874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pharmacogenetics and cancer therapy

1 reference

https://pubmed.ncbi.nlm.nih.gov/15480874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial inactivation of the RB product in a family with incomplete penetrance of familial retinoblastoma and benign retinal tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/15480874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular diagnosis of familial adenomatous polyposis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15480874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pyrosequencing?-based SNP allele frequency estimation in DNA pools

1 reference

https://pubmed.ncbi.nlm.nih.gov/15480874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

When the message goes awry: disease-producing mutations that influence mRNA content and performance.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15480874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

F-SSCP: fluorescence-based polymerase chain reaction-single-strand conformation polymorphism (PCR-SSCP) analysis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15480874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA methylation: past, present and future directions

1 reference

https://pubmed.ncbi.nlm.nih.gov/15480874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distinct RB1 gene mutations with low penetrance in hereditary retinoblastoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/15480874

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10038-004-0201-0

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 September 2017

ResearchGate publication ID

0 references

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