Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Gene dosage effect in acquired monosomy 7: distinct behaviour of beta-glucuronidase and phosphoserine phosphatase.

Genes, chromosomes & cancer - 1 Jan 1990

Minelli A, Piantanida M, Maserati E, Campagnoli E, Pasquali F, Danesino C

Abstract excerpt

Evidence for gene dosage effect for beta-glucuronidase (GUSB) and phosphoserine phosphatase (PSP), whose genes are mapped on chromosome 7, was searched in a group of 13 patients with myeloproliferative disorders and acquired monosomy 7. The monosomy 7 was the sole anomaly in nine patients and was associated with other chromosome changes in four. A group of 19 patients with similar diseases but with normal...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Alleles
Share to Chromosomes, Human, Pair 7

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Enzyme Induction

Share to Gene Expression Regulation, Neoplastic

Share to Genetic Markers

Share to Leukemia, Myelogenous, Chronic, BCR-ABL Positive

Share to Leukemia, Myeloid, Acute

Share to Neoplasm Proteins

Source

Identifiers

PMID: 1964582
DOI: 10.1002/gcc.2870010305

Genes

GUSB

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 9 closest

Gene dosage effect in acquired monosomy 7: distinct behaviour of beta-glucuronidase and phosphoserine phosphatase.PMID 1964582Read ↗

Familial partial monosomy 7 and myelodysplasia: different parental origin of the monosomy 7 suggests action of a mutator gene.Semantic proximity Read ↗

Hypogammaglobulinemia and Silver-Russell phenotype associated with partial trisomy 7q and partial monosomy 21q.Semantic proximity Read ↗

Loss of maternal allele in a child with myelodysplastic syndrome and monosomy 7.Semantic proximity Read ↗

No evidence for isolated imprinting mutations in the PEG1/MEST locus in Silver-Russell patients.Semantic proximity Read ↗

A multiplex methylation PCR assay for identification of uniparental disomy of chromosome 7.Semantic proximity Read ↗

Granulocyte colony-stimulating factor preferentially stimulates proliferation of monosomy 7 cells bearing the isoform IV receptorSemantic proximity Read ↗

Possible evidence for genomic imprinting in childhood acute myeloblastic leukaemia associated with monosomy for chromosome 7.Semantic proximity Read ↗

The presentation of nephrotic syndrome during immunosuppressive treatment for aplastic anemia with monosomy 7 in a 16-year-old boy: a case reportSemantic proximity Read ↗

Mutations of the ras proto-oncogenes in childhood monosomy 7.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.