Anticipation in familial leukemia (Q24675558)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8900225 AND SRC:MED&resulttype=core&format=json

20 October 2019

title

Anticipation in familial leukemia (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8900225 AND SRC:MED&resulttype=core&format=json

20 October 2019

1 reference

2

E L Goode

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8900225 AND SRC:MED&resulttype=core&format=json

20 October 2019

author name string

M Horwitz

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8900225 AND SRC:MED&resulttype=core&format=json

20 October 2019

G P Jarvik

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8900225 AND SRC:MED&resulttype=core&format=json

20 October 2019

language of work or name

English

0 references

publication date

1 November 1996

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8900225 AND SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

20 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8900225 AND SRC:MED&resulttype=core&format=json

20 October 2019

volume

59

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8900225 AND SRC:MED&resulttype=core&format=json

20 October 2019

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8900225 AND SRC:MED&resulttype=core&format=json

20 October 2019

page(s)

990-998

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8900225 AND SRC:MED&resulttype=core&format=json

A human homologue of Saccharomyces cerevisiae SNF2/SWI2 and Drosophila brm genes potentiates transcriptional activation by the glucocorticoid receptor

20 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914843

Simple tandem DNA repeats and human genetic disease

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914843

Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914843

Trinucleotide repeat expansion in neurological disease

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914843

A gene for familial total anomalous pulmonary venous return maps to chromosome 4p13-q12.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914843

Unstable triplet repeat sequences: a source of cancer mutations?

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914843

Molecular pathogenesis of the chromosome 16 inversion in the M4Eo subtype of acute myeloid leukemia.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914843

Anticipation and instability of IT-15 (CAG)n repeats in parent-offspring pairs with Huntington disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914843

Genetic instability of a dinucleotide repeat-rich region in three hematologic malignancies

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914843

Structure of the leukemia-associated human CBFB gene

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914843

Genetic instability of microsatellites in hematological neoplasms

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914843

Lymphatic leukemia in father and son

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914843

An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914843

Studies of a familial platelet disorder

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914843

Absence of hereditary p53 mutations in 10 familial leukemia pedigrees

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914843

Anticipation in myotonic dystrophy: new light on an old problem

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914843

Cytogenetic and molecular analysis of chromosome 11q23 abnormalities in leukaemia

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914843

Familial Monocytic Leukaemia A Report of Two Families

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914843

Thirteen Cases of Leukemia in a Family 2

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914843

Anticipation in myotonic dystrophy: fact or fiction?

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914843

An in-frame trinucleotide repeat in the coding region of the human cellular glutathione peroxidase (GPX1) gene: in vivo polymorphism and in vitro instability

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914843

Basal components of the transcription apparatus (RNA polymerase II, TATA-binding protein) contain activation domains: is the repetitive C-terminal domain (CTD) of RNA polymerase II a "portable enhancer domain"?

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914843

Genetic relationships in familial leukemia and lymphoma.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914843

Possible inherited leukaemogenic factors in familial acute myelogenous leukaemia

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914843

Acute leukemia and preleukemia in eight males in a family: An X-linked disorder?

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914843

Molecular genetics of hereditary ataxias

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914843

Statistical pitfalls in detecting age-of-onset anticipation: the role of correlation in studying anticipation and detecting ascertainment bias

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914843

Familial myelodysplastic syndrome with onset late in life

28 November 2018

1 reference

12 December 2020

Patterns of familial leukemia. Ten cases of leukemia in two interrelated families

1 reference

12 December 2020

Varied manifestations of a familial lymphoproliferative disorder

1 reference

12 December 2020

Lymphocyte studies in familial chronic lymphatic leukemia

1 reference

12 December 2020

Ataxia-pancytopenia: syndrome of cerebellar ataxia, hypoplastic anemia, monosomy 7, and acute myelogenous leukemia

1 reference

12 December 2020

Familial leukemia and aplastic anemia associated with monosomy 7

1 reference

12 December 2020

Familial chronic lymphocytic leukemia

1 reference

12 December 2020

Inherited platelet-storage pool deficiency associated with a high incidence of acute myeloid leukaemia

1 reference

12 December 2020

Genetic mechanism of leukemia predisposition in a family with 7 cases of acute myeloid leukemia

1 reference

12 December 2020

No evidence for association of familial Parkinson's disease with CAG repeat expansion

1 reference

12 December 2020

Mutator phenotype in a subset of chronic lymphocytic leukemia

1 reference

12 December 2020

Psychosis and genes with trinucleotide repeat polymorphism

1 reference

12 December 2020

Familial myeloid leukemia associated with loss of the long arm of chromosome 5

1 reference

12 December 2020

Linkage of a familial platelet disorder with a propensity to develop myeloid malignancies to human chromosome 21q22.1-22.2

1 reference

12 December 2020

A family inheriting different subtypes of acute myelogenous leukemia

1 reference

12 December 2020

Chronic lymphocytic leukemia in a family, including twin brothers and a son

1 reference

12 December 2020

1 reference

12 December 2020

HEREDITARY FACTORS IN HUMAN LEUKAEMIA: A REPORT OF FOUR CASES OF LEUKAEMIA IN A FAMILY

1 reference

12 December 2020

FAMILIAL LEUKEMIA; FIVE CASES OF ACUTE LEUKEMIA IN THREE GENERATIONS

1 reference

12 December 2020

Familial Hodgkin's disease: its significance and implications

1 reference

12 December 2020

Chromosomal disorder and neoplastic diseases in a family with inherited fragile 16. Causality or casualty?

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8900225 AND SRC:MED&resulttype=core&format=json

20 October 2019

PubMed publication ID

8900225

1 reference