(Q42793617)

English

Isothermal multiple displacement amplification: a highly reliable approach for generating unlimited high molecular weight genomic DNA from clinical specimens

scientific article published on August 2004

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

7 November 2017

Isothermal multiple displacement amplification: a highly reliable approach for generating unlimited high molecular weight genomic DNA from clinical specimens (English)

1 reference

Europe PubMed Central

PMC publication ID

7 November 2017

author name string

Rajyalakshmi Luthra

1

1 reference

Europe PubMed Central

PMC publication ID

7 November 2017

L Jeffrey Medeiros

2

1 reference

Europe PubMed Central

PMC publication ID

7 November 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

1 August 2004

1 reference

Europe PubMed Central

PMC publication ID

7 November 2017

The Journal of Molecular Diagnostics

1 reference

Europe PubMed Central

PMC publication ID

7 November 2017

6

1 reference

Europe PubMed Central

PMC publication ID

7 November 2017

3

1 reference

Europe PubMed Central

PMC publication ID

7 November 2017

236-242

1 reference

Europe PubMed Central

PMC publication ID

7 November 2017

Whole genome analysis of genetic alterations in small DNA samples using hyperbranched strand displacement amplification and array-CGH.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867643

27 May 2018

Quantification of bcl-2/JH fusion sequences and a control gene by multiplex real-time PCR coupled with automated amplicon sizing by capillary electrophoresis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867643

27 May 2018

Comprehensive human genome amplification using multiple displacement amplification

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867643

27 May 2018

Activating mutation of D835 within the activation loop of FLT3 in human hematologic malignancies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867643

27 May 2018

Overview of the role of molecular methods in the diagnosis of malignant lymphomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867643

27 May 2018

Novel 5' exonuclease-based real-time PCR assay for the detection of t(14;18)(q32;q21) in patients with follicular lymphoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867643

27 May 2018

Genomic DNA amplification and the detection of t(2;5)(p23;q35) in lymphoid neoplasms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867643

27 May 2018

Isothermal strand-displacement amplification applications for high-throughput genomics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867643

16 August 2018

PCR analysis of immunoglobulin heavy chain (IgH) and TcR-gamma chain gene rearrangements in the diagnosis of lymphoproliferative disorders: results of a study of 525 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/15269301

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel four-color PCR assay to assess T-cell receptor gamma gene rearrangements in lymphoproliferative lesions

1 reference

https://pubmed.ncbi.nlm.nih.gov/15269301

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparison of different polymerase chain reaction-based approaches for clonality assessment of immunoglobulin heavy-chain gene rearrangements in B-cell neoplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/15269301

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RAS mutations are rare events in Philadelphia chromosome-negative/bcr gene rearrangement-negative chronic myelogenous leukemia, but are prevalent in chronic myelomonocytic leukemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/15269301

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prognostic implication of FLT3 and N-RAS gene mutations in acute myeloid leukemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/15269301

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/S1525-1578(10)60516-8

1 reference

Europe PubMed Central

PMC publication ID

7 November 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

7 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

7 November 2017

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