Skip to search formSkip to main contentSkip to account menu

t(1;19)

A cytogenetic abnormality that involves a translocation between chromosomes 1 and 19.
National Institutes of Health

Related topics

Related topics

2 relations
Chromosomes, Human, Pair 1Chromosomes, Human, Pair 19

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2012
2012
Immunophenotype and cytogenetic characteristics in the relationship between birth weight and childhood leukemia
High birth weight increases the risk of childhood acute lymphoid leukemia (ALL) through unknown mechanisms. Whether this risk is… 
Highly Cited
2002
Highly Cited
2002
Gradient of E2A Activity in B-Cell Development
ABSTRACT The E2A locus is a frequent target of chromosomal translocations in B-cell acute lymphoblastic leukemia (B-ALL). E2A… 
1997
1997
Regional cancer cytogenetics: a report on 1,143 diagnostic cases.
Highly Cited
1995
Highly Cited
1995
Mutations of the p53 and ras genes in childhood t(1;19)-acute lymphoblastic leukemia.
We have investigated the alterations of p53 and ras genes including H-, K-, and N-ras genes in 22 acute lymphoblastic leukemia… 
1993
1993
Age- and gender-related heterogeneity of cancer chromosome aberrations.
1993
1993
Human t(1;19)(q23;p13) pre-B acute lymphoblastic leukemia in mice with severe combined immunodeficiency.
Severe combined immunodeficient (SCID) mice were injected intravenously with 5 x 10(6) primary bone marrow (BM) blasts from newly… 
Highly Cited
1990
Highly Cited
1990
Molecular analysis of the t(1;19) breakpoint cluster region in pre‐b cell acute lymphoblastic leukemias
The t(1;19) chromosomal translocation in acute lymphoblastic pre‐B cell leukemias involves the gene E2A for helix‐loop‐helix (HLH… 
Highly Cited
1989
Highly Cited
1989
The gene for enhancer binding proteins E12/E47 lies at the t(1;19) breakpoint in acute leukemias.
The gene (E2A) that codes for proteins with the properties of immunoglobulin enhancer binding factors E12/E47 was mapped to… 
Highly Cited
1989
Highly Cited
1989
Definition of subchromosomal intervals around the myotonic dystrophy gene region at 19q.
1986
1986
A t(1;19) chromosome translocation in three cases of human malignant melanoma.
Abnormalities of chromosome 1, including trisomy for all or a portion of the long arm, have been frequently reported in many… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)