Evidence map›Paper›PMID 8644714›Full record

ArticleAmerican journal of human genetics1996

Isolation of a cosmid clone corresponding to an inv(21) breakpoint of a patient with transient abnormal myelopoiesis.

T Ohta, M Nakano, T Tsujita, K Abe, K Osoegawa, T Yamagata, K Yoshiura, Y Jinno, E Soeda, Y Nakamura and 1 more

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In one paragraph

Article in American journal of human genetics, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
2.2field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 14 citations in OpenAlex.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

T OhtaDepartment of Human Genetics, Nagasaki University School of Medicine, Tokyo, Japan.
M Nakano
T Tsujita
K Abe
K Osoegawa
T Yamagata
K Yoshiura
Y Jinno
E Soeda
Y Nakamura
N Niikawa
University of Nagasaki · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transient abnormal myelopoiesis (TAM) is a leukemoid reaction occurring occasionally on Down syndrome (DS) newborn infants. It has been hypothesized that "disomic homozygosity" in 21-trisomic cells plays an important role in the genesis of TAM, and the putative TAM gene was suggested to be mapped at a 21q11 region. We encountered a DS-associated TAM infant with a 47,XY,inv(21)(q11.1q22.13),+inv(21)(q11.1q22.13) karyotype. On the basis of another presumption that in this patient the putative TAM gene is disrupted by the break, we tried to isolate a breakpoint DNA. FISH analysis with cosmid clones corresponding to various sequence-tagged-site (STS) markers mapped at around 21q11.1-q11.2, we confirmed that the proximal breakpoint of the inv(21) was located between two STSs, G51E07 and D21S215, the latter locus being consistent with the previous tentative mapping. After construction of a cosmid contig encompassing between the two markers, we have isolated a cosmid clone corresponding to the proximal breakpoint of the inversion. This breakpoint was located near a previously identified duplicated region that is homologous to the sequence at 21q22.1. The isolated cosmid clone is useful for analysis of other TAM patients and for a search for a transcript at or flanking the breakpoint.

Indexed as

Chromosome InversionChromosomes, Human, Pair 21AdultBase SequenceChromosome WalkingCloning, MolecularCosmidsDown SyndromeFemaleHumansInfant, NewbornMaleMolecular Sequence DataMyeloproliferative DisordersSequence Tagged Sites

Identifiers

PMID8644714
PMCPMC1914556
OpenAlexW79195967

What OpenQuestion holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.