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

Paternal imprinting of the SLC22A1LS gene located in the human chromosome segment 11p15.5.

BMC genetics - 3 Jun 2004

Bajaj Vineeta, Markandaya Manjunath, Krishna Lingegowda, Kumar Arun

Abstract excerpt

BACKGROUND: Genomic imprinting is an epigenetic chromosomal modification in the gametes or zygotes that results in a non-random monoallelic expression of specific autosomal genes depending upon their parent of origin. Approximately 44 human genes have been reported to be imprinted. A majority of them are clustered, including some on chromosome segment 11p15.5. We report here the imprinting status of the SLC22A1LS...

Read the complete abstract on PubMed

Topics

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

Share to Abortion, Spontaneous
Share to Chromosomes, Human, Pair 11
Share to Fetus

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Expression Regulation, Developmental

Share to Genetic Carrier Screening

Share to Genomic Imprinting

Share to Point Mutation

Share to Polymorphism, Single-Stranded Conformational

Source

Open in PubMed Open full text

Identifiers

PMID: 15175115
DOI: 10.1186/1471-2156-5-13
PMCID: PMC425576

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 10 closest

Paternal imprinting of the SLC22A1LS gene located in the human chromosome segment 11p15.5.PMID 15175115Read ↗

The IPL Gene on Chromosome 11p15.5 is Imprinted in Humans and Mice and is Similar to TDAG51, Implicated in Fas Expression and ApoptosisSemantic proximity Read ↗

Genomic loss of imprinting in first-trimester human placenta.Semantic proximity Read ↗

Assessment of genomic imprinting of SLC38A4, NNAT, NAP1L5, and H19 in cattle.Semantic proximity Read ↗

Genomic imprinting of a human apoptosis gene homologue, TSSC3.Semantic proximity Read ↗

Occasional loss of constitutive heterozygosity at 11p15.5 and imprinting relaxation of the IGFII maternal allele in hepatoblastoma.Semantic proximity Read ↗

Somatic mutation of TSSC5, a novel imprinted gene from human chromosome 11p15.5.Semantic proximity Read ↗

Selective maternal-allele loss in human lung cancers of the maternally expressed p57KIP2 gene at 11p15.5.Semantic proximity Read ↗

Loss of imprinted genes and paternal SUR1 mutations lead to hyperinsulinism in focal adenomatous hyperplasia.Semantic proximity Read ↗

Relaxation of imprinting of human insulin-like growth factor II gene, IGF2, in sporadic breast carcinomas.Semantic proximity Read ↗

Repeat-directed isolation of a novel gene preferentially expressed from the maternal allele in human placenta.Semantic proximity Read ↗

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