Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 225,206,854 papers from all fields of science
Search
Sign In
Create Free Account
6p22.1
A chromosome band present on 6p
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
5 relations
Chromosome 6 Short Arm
Chromosomes
GMNN wt Allele
HIST1H3B wt Allele
Expand
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Cross-Cancer Pleiotropic Analysis Reveals Novel Susceptibility Loci for Lung Cancer
Lijuan Wang
,
Meng Zhu
,
+10 authors
Hongbing Shen
Frontiers in Oncology
2020
Corpus ID: 210173008
Genome-wide association studies (GWASs) have identified hundreds of single nucleotide polymorphisms (SNPs) associated with cancer…
Expand
2017
2017
Genome-wide association study of wheezing phenotypes in the Avon longitudinal study of parents and children
R. Granell
,
J. Henderson
,
J. Sterne
2017
Corpus ID: 56935007
Asthma is a polygenic heterogeneous condition with phenotypic variation through the life course. Using 5 wheezing phenotypes from…
Expand
2015
2015
Single Nucleotide Polymorphisms (5p15.33, 6p22.1 and 15q25.1), Smoking and Lung Cancer Survival
Wen Zhang
2015
Corpus ID: 79495433
Background: Genome-wide studies of single nucleotide polymorphisms (SNPs) reported associations between chromosomal regions (5p15…
Expand
2014
2014
DNA methylation analysis of the evolution of Wilms tumour from its precursor nephrogenic rests
J. Charlton
2014
Corpus ID: 82015930
Recurrent loss of imprinting at 11p15, paucity of recurrent genetic mutations and associated nephrogenic rests (NR; precursor…
Expand
2010
2010
Candidate variants at 6p21.33 and 6p22.1 and risk of non-small cell lung cancer in a Chinese population.
Mingfeng Zhang
,
Lingmin Hu
,
+7 authors
Hongbing Shen
International Journal of Molecular Epidemiology…
2010
Corpus ID: 27277036
Chromosome 6p21.33, containing BAT3 and MSH5 genes, together with chromosome 6p22.1 were recently identified as susceptible…
Expand
Highly Cited
2006
Highly Cited
2006
Chromosomal Translocations Fusing the BCL6 Gene to Different Partner Loci Are Recurrent in Primary Central Nervous System Lymphoma and May Be Associated With Aberrant Somatic Hypermutation or…
H. Schwindt
,
T. Akasaka
,
+6 authors
M. Deckert
Journal of Neuropathology and Experimental…
2006
Corpus ID: 27233370
Abstract Primary central nervous system lymphomas (PCNSLs) are diffuse large B cell lymphomas confined to the brain. Only minimal…
Expand
2001
2001
[Preliminary study of the gene structure of human glycosylphosphatidylinositol specific phospholipase D].
J. Tang
,
S. Gu
,
X. Zhang
Hunan yi ke da xue xue bao = Hunan yike daxue…
2001
Corpus ID: 41635510
To explore the cDNA and its genomic gene structure of human glycosylphosphatidylinositol specific phospholipase D (GPI-PLD), the…
Expand
1999
1999
Monosomy 6 in human cultured fibroblast-like cells permanently stimulated by fibroblast growth factor 1: evidence for selection
H. Kehrer-Sawatzki
,
H. Röck
,
H. Götz
,
A. Siegel
,
W. Krone
Cytogenetic and Genome Research
1999
Corpus ID: 23167377
The appearance of cells with monosomy 6 (mono6 cells) in cultures of human fibroblast-like cells during long-term stimulation…
Expand
1997
1997
Physical mapping of two histone gene clusters on human chromosome 6p22.1-22.2.
A. Volz
,
W. Albig
,
D. Doenecke
,
A. Ziegler
DNA Sequence
1997
Corpus ID: 38921068
Histones are basic proteins which are responsible for the assembly and maintenance of the nucleosomal structure within the…
Expand
Review
1997
Review
1997
The mouse HFE gene
P. Riegert
,
S. Gilfillan
,
I. Nanda
,
M. Schmid
,
S. Bahram
Immunogenetics
1997
Corpus ID: 28901121
Idiopathic hemochromatosis is believed to represent the most frequent hereditary condition in Caucasian populations (for review…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE
or Only Accept Required