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5q31.3
A chromosome band present on 5q
National Institutes of Health
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4 relations
Chromosomes
FCHSD1 wt Allele
UBE2D2 wt Allele
chromosome 5q
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2017
Review
2017
The role of Purα in neuronal development, the relationship between Purα and epilepsy in the current researches
Shanshan Guo
,
Bingying Zhang
,
C. Yuan
,
Ping Li
,
T. Sun
,
Jianqi Cui
2017
Corpus ID: 29166588
As a ubiquitous protein in the body, Purα has been considered to possess multiple regulatory functions from DNA replication and…
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2014
2014
Cytogenetically normal uterine leiomyomas without MED12-mutations – a source to identify unknown mechanisms of the development of uterine smooth muscle tumors
C. Holzmann
,
D. N. Markowski
,
D. Koczan
,
W. Küpker
,
B. Helmke
,
Jörn Bullerdiek
Molecular Cytogenetics
2014
Corpus ID: 255985915
Recent findings on genetic changes in uterine leiomyomas suggest these benign tumors being a heterogeneous group of diseases in…
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2013
2013
Treacher- Collins Syndrome unusually in siblings
Apeksha Dhole
,
Bhavana Agrawal
,
A. Parate
2013
Corpus ID: 12159616
Treacher- Collins Syndrome (TCS) is a rare autosomal dominant disorder of craniofacial morphogenesis. The frequency of TCS is 1…
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2011
2011
ANKHD1 Silencing Induces S-Phase Arrest and Modulates Cell Cycle Gene Expression in Human Myeloma Cells
A. Dhyani
,
A. Duarte
,
P. Favaro
,
S. Saad
2011
Corpus ID: 208437022
Abstract 1828 ANKHD1 is a multiple ankyrin repeats containing protein with a single KH domain. It is a large protein (∼ 280 kDa…
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2011
2011
Gewinne und Verluste von 5q31.3, 5p15.33 und Chromosom X und deren klinische Relevanz bei TEL-AML1 positiven und negativen Erstrezidiven der akuten lymphoblastischen Leukämie im Kindesalter
Franziska Meyr
2011
Corpus ID: 161907293
2006
2006
5q Deletions Can Be Identified Based on the Expression Level of 5q Genes: A Study on 49 Cases with MDS or AML Analysed in Parallel by Gene Expression Profiling and Genomic Arrays.
C. Schoch
,
Sonja Rauhut
,
S. Schnittger
,
F. Dicker
,
W. Kern
,
T. Haferlach
2006
Corpus ID: 208402453
Deletions of the long arm of chromosome 5 are typical aberrations in AML and MDS. They occur either as the sole abnormality or…
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