MOLECULAR DELINEATION OF THE CRITICAL REGION OF THE 5Q-CHROMOSOME IN THE 5Q-SYNDROME

MOLECULAR DELINEATION OF THE CRITICAL REGION OF THE 5Q-CHROMOSOME IN THE 5Q-SYNDROME

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς:	Boultwood, J, Fidler, C, Lewis, S, Maccarthy, A, Kelly, S, Sheridan, H, Littlewood, T, Buckle, V, Wainscoat, J
Μορφή:	Journal article
Έκδοση:	1993

Παρόμοια τεκμήρια

MOLECULAR MAPPING OF UNCHARACTERISTICALLY SMALL 5Q DELETIONS IN 2 PATIENTS WITH THE 5Q- SYNDROME - DELINEATION OF THE CRITICAL REGION ON 5Q AND IDENTIFICATION OF A 5Q- BREAKPOINT
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Molecular mapping of uncharacteristically small 5q deletions in two patients with the 5q- syndrome: delineation of the critical region on 5q and identification of a 5q- breakpoint.
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Allelic loss of IRF1 in myelodysplasia and acute myeloid leukemia: retention of IRF1 on the 5q- chromosome in some patients with the 5q- syndrome.
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Molecular cytogenetic delineation of the critical deleted region in the 5q- syndrome.
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ISOLATION OF NOVEL CDNA CLONES MAPPING TO THE CRITICAL REGION OF THE 5Q-CHROMOSOME IN THE 5Q-SYNDROME
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The 5q-syndrome.
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MOLECULAR MAPPING OF THE 7Q-DELETION IN MYELOID DISORDERS
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The human POP2 gene: identification, sequencing, and mapping to the critical region of the 5q- syndrome.
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Narrowing the critical deleted region in the 5q-syndrome.
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5q- syndrome.
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NRAS, FLT3 and TP53 mutations in patients with myelodysplastic syndrome and a del(5q).
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Narrowing and genomic annotation of the critical region of the 5q-syndrome.
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Physical mapping of the human ATX1 homologue (HAH1) to the critical region of the 5q- syndrome within 5q32, and immediately adjacent to the SPARC gene.
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Molecular analysis of the 5q-syndrome
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Primary transcription map of the critical region of the 5q-syndrome.
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Novel genes mapping to the critical region of the 5q- syndrome.
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Isolation and analysis of novel candidate genes mapping to the critical region of the 5q-syndrome.
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Molecular characterization of the 7q deletion in myeloid disorders.
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Mutation analysis of the SPARC gene in the 5q-syndrome.
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Isolation and analysis of novel genes mapping to the critical region of the 5q-syndrome
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Gene expression profiling in 5q-syndrome and myelodysplastic syndromes.
ανά: Pellagatti, A, κ.ά.
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Narrowing and genomic annotation of the commonly deleted region of the 5q- syndrome.
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Combined immunophenotyping and FISH identifies the involvement of B-cells in 5q- syndrome.
ανά: Jaju, R, κ.ά.
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Haploinsufficiency of ribosomal proteins and p53 activation in anemia: Diamond-Blackfan anemia and the 5q- syndrome.
ανά: Boultwood, J, κ.ά.
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Transcription mapping of the 5q- syndrome critical region: cloning of two novel genes and sequencing, expression, and mapping of a further six novel cDNAs.
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RECENT ADVANCES IN THE 5Q- SYNDROME
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Molecular characterization of the chromosome 9q deletion in AML.
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The role of haploinsufficiency of RPS14 and p53 activation in the molecular pathogenesis of the 5q- syndrome.
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Gene expression profiling of CD34+ cells in patients with the 5q- syndrome.
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Activation of the mTOR pathway by the amino acid (L)-leucine in the 5q- syndrome and other ribosomopathies.
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Expression profiling of CD34+cells in patients with myelodysplastic syndromes with and without a del(5q).
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Haploinsufficiency of RPS14 in 5q- syndrome is associated with deregulation of ribosomal- and translation-related genes.
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Whole chromosome painting and FISH with subtelomeric probes reveals cryptic chromosome rearrangements in del(5q) leukaemias: a UK Cancer Cytogenetic Group study
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A new recurrent translocation, t(5;11)(q35;p15.5), associated with del(5q) in childhood AML.
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The role of haploinsufficiency of RPS14 and p53 activation in the molecular pathogenesis of the 5q- syndrome
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