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Leukemia (5)
Oncogene (4)
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Research (16)

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Showing 1–16 of 16 results

Advanced filters: Author: D M Lillington Clear advanced filters

Alternative splicing in wild-type AF10 and CALM cDNAs and in AF10-CALM and CALM-AF10 fusion cDNAs produced by the t(10;11)(p13–14;q14–q21) suggests a potential role for truncated AF10 polypeptides

CC Silliman
L McGavran
SP Hunger
Research02 Sept 1998
Leukemia

Volume: 12, P: 1404-1410
Chromosome abnormalities and MLL rearrangements in acute myeloid leukemia of infants

N Satake
N Maseki
Y Kaneko
Research22 Jul 1999
Leukemia

Volume: 13, P: 1013-1017
Chimeric MLL products with a Ras binding cytoplasmic protein AF6 involved in t(6;11) (q27;q23) leukemia localize in the nucleus

Tatsuroh Joh
Kazuhito Yamamoto
Masao Seto
Research02 Oct 1997
Oncogene

Volume: 15, P: 1681-1687
Detection of an insertion deletion of region 8q13-q21.2 in a patient with Duane syndrome: implications for mapping and cloning a Duane gene

G Calabrese
L Stuppia
B Dallapiccola
Research29 Jun 1998
European Journal of Human Genetics

Volume: 6, P: 187-193
Array comparative genomic hybridization analysis of olfactory neuroblastoma

Mohamed Guled
Samuel Myllykangas
Edward B Stelow
Research11 Apr 2008
Modern Pathology

Volume: 21, P: 770-778
Effective assembly of fimbriae in Escherichia coli depends on the translocation assembly module nanomachine

The translocation assembly module (TAM) of Escherichia coli functions together with the BAM complex to mediate the rapid assembly of usher proteins, the molecular platform important for the biogenesis of bacterial fimbriae.

Christopher Stubenrauch
Matthew J. Belousoff
Trevor Lithgow
Research16 May 2016
Nature Microbiology

Volume: 1, P: 1-8
Immunophenotypic patterns and cytogenetic anomalies in acute non-lymphoblastic leukemia subtypes: a prospective study of 432 patients

RO Casasnovas
L Campos
E Solary
Research01 Apr 1998
Leukemia

Volume: 12, P: 34-43
Genetic aberrations in glioblastoma multiforme: translocation of chromosome 10 in an O-2A-like cell line

X Mao
T A Jones
D Sheer
ResearchOpen Access29 Jan 1999
British Journal of Cancer

Volume: 79, P: 724-731
Clinical and biological characteristics of adult de novo and secondary acute myeloid leukemia with balanced 11q23 chromosomal anomaly or MLL gene rearrangement compared to cases with unbalanced 11q23 anomaly: confirmation of the existence of different entities with 11q23 breakpoint

E Archimbaud
C Charrin
R Rimokh
Research01 Apr 1998
Leukemia

Volume: 12, P: 25-33
Selective inhibition of apoptosis by TPA-induced differentiation of U937 leukemic cells

Olivier Sordet
Ali Bettaieb
Eric Solary
Research09 Apr 1999
Cell Death & Differentiation

Volume: 6, P: 351-361
High level amplification of N-MYC is not associated with adverse histology or outcome in primary retinoblastoma tumours

D M Lillington
L K Goff
B D Young
ResearchOpen Access23 Sept 2002
British Journal of Cancer

Volume: 87, P: 779-782
LGR5 is a conserved marker of hair follicle stem cells in multiple species and is present early and throughout follicle morphogenesis

Kathryn M. Polkoff
Nithin K. Gupta
Jorge A. Piedrahita
ResearchOpen Access01 Jun 2022
Scientific Reports

Volume: 12, P: 1-11
The cloning, mapping and expression of a novel gene, BRL, related to the AF10 leukaemia gene

Paul McCullagh
Tracy Chaplin
Bryan D Young
Research09 Dec 1999
Oncogene

Volume: 18, P: 7442-7452
MicroRNA miR-181a correlates with morphological sub-class of acute myeloid leukaemia and the expression of its target genes in global genome-wide analysis

S Debernardi
S Skoulakis
B D Young
Research01 Mar 2007
Leukemia

Volume: 21, P: 912-916
Sequential genetic change at the TP53 and chemokine receptor CXCR4 locus during transformation of human ovarian surface epithelium

K M Archibald
H Kulbe
F Balkwill
Research23 Jan 2012
Oncogene

Volume: 31, P: 4987-4995
Molecular analysis of an unstable genomic region at chromosome band 11q23 reveals a disruption of the gene encoding the α2 subunit of platelet-activating factor acetylhydrolase (Pafah1a2) in human lymphoma

Nathalie Lecointe
Joanne Meerabux
Bryan D Young
Research20 May 1999
Oncogene

Volume: 18, P: 2852-2859

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Alternative splicing in wild-type AF10 and CALM cDNAs and in AF10-CALM and CALM-AF10 fusion cDNAs produced by the t(10;11)(p13–14;q14–q21) suggests a potential role for truncated AF10 polypeptides

Chromosome abnormalities and MLL rearrangements in acute myeloid leukemia of infants

Chimeric MLL products with a Ras binding cytoplasmic protein AF6 involved in t(6;11) (q27;q23) leukemia localize in the nucleus

Detection of an insertion deletion of region 8q13-q21.2 in a patient with Duane syndrome: implications for mapping and cloning a Duane gene

Array comparative genomic hybridization analysis of olfactory neuroblastoma

Effective assembly of fimbriae in Escherichia coli depends on the translocation assembly module nanomachine

Immunophenotypic patterns and cytogenetic anomalies in acute non-lymphoblastic leukemia subtypes: a prospective study of 432 patients

Genetic aberrations in glioblastoma multiforme: translocation of chromosome 10 in an O-2A-like cell line

Clinical and biological characteristics of adult de novo and secondary acute myeloid leukemia with balanced 11q23 chromosomal anomaly or MLL gene rearrangement compared to cases with unbalanced 11q23 anomaly: confirmation of the existence of different entities with 11q23 breakpoint

Selective inhibition of apoptosis by TPA-induced differentiation of U937 leukemic cells

High level amplification of N-MYC is not associated with adverse histology or outcome in primary retinoblastoma tumours

LGR5 is a conserved marker of hair follicle stem cells in multiple species and is present early and throughout follicle morphogenesis

The cloning, mapping and expression of a novel gene, BRL, related to the AF10 leukaemia gene

MicroRNA miR-181a correlates with morphological sub-class of acute myeloid leukaemia and the expression of its target genes in global genome-wide analysis

Sequential genetic change at the TP53 and chemokine receptor CXCR4 locus during transformation of human ovarian surface epithelium

Molecular analysis of an unstable genomic region at chromosome band 11q23 reveals a disruption of the gene encoding the α2 subunit of platelet-activating factor acetylhydrolase (Pafah1a2) in human lymphoma

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