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8q22.1
A chromosome band present on 8q
National Institutes of Health
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Related topics
Related topics
4 relations
CCNE2 wt Allele
Chromosomes
LAPTM4B wt Allele
MTDH wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Response to: ‘Mutation in MMP2 gene may result in scleroderma-like skin thickening’ by Bader-Meunier et al
S. Banka
,
W. G. Newman
Annals of the Rheumatic Diseases
2015
Corpus ID: 206851875
MMP2 related disease (Multicentric osteolysis, nodulosis and arthropathy—MONA syndrome—OMIM #259600) consists of a continuous…
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2015
2015
Correction: Selectivity in Genetic Association with Sub-classified Migraine in Women
D. Chasman
,
V. Anttila
,
J. Buring
,
P. Ridker
,
M. Schürks
,
T. Kurth
PLoS Genetics
2015
Corpus ID: 54561268
Incorrect date for reference [13]: The date for reference [13] is incorrect. The correct date is 2010, not 2013. The correct…
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2013
2013
Integrative analysis of copy number alteration and gene expression profiling in ovarian clear cell adenocarcinoma.
C. Sung
,
C. Choi
,
+11 authors
Byoung-Gie Kim
Cancer Genetics
2013
Corpus ID: 22281805
2012
2012
A genotype–phenotype analysis of the 8q22.1 variant in migraine with aura
A. Esserlind
,
M. Kirchmann
,
A. Hauge
,
H. Le
,
J. Olesen
European Journal of Neurology
2012
Corpus ID: 1563051
Background and purpose: Although the genetics of familial hemiplegic migraine are being unraveled, this is not the case for the…
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2010
2010
News on migraine: genetics, genetics, and aortic stiffness
M. Strupp
Journal of Neurology
2010
Corpus ID: 8548983
Migraine is the most frequent episodic neurological disorder. In Europe about 8% of males and 17% of females are affected. It has…
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2009
2009
Linkage analysis of schizophrenia in African-American families
H. Wiener
,
L. Klei
,
+18 authors
R. Go
Schizophrenia Research
2009
Corpus ID: 22524441
2009
2009
Shadow autozygosity mapping by linkage exclusion (SAMPLE): a simple strategy to identify the genetic basis of lethal autosomal recessive disorders
I. Carr
,
K. Szymanska
,
E. Sheridan
,
A. Markham
,
D. Bonthron
,
Colin A. Johnson
Human Mutation
2009
Corpus ID: 21144604
Autozygosity mapping has been invaluable for determining the genetic basis of lethal autosomal recessive disorders, but this…
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2009
2009
16-P021 Isolation of NOCE, a novel node and notochord-specific enhancer element from the Noto locus
Leonie Alten
,
K. Schuster‐Gossler
,
Anja Beckers
,
A. Gossler
Mechanisms of Development
2009
Corpus ID: 16708364
2004
2004
[Linkage analysis in an extended multigenerational family segregating for idiopathic epilepsy].
L. Palacio
,
J. Sánchez
,
M. Jiménez
,
D. Rivera-Valencia
,
I. Jiménez-Ramírez
,
O. M. Arcos
Revista de neurología (Ed. impresa)
2004
Corpus ID: 20150978
INTRODUCTION Linkage analyses enable us to identify the loci that bestow susceptibility to certain diseases which are assumed to…
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1994
1994
Integration site of human papillomavirus type‐18 DNA in chromosome band 8q22.1 of C4‐1 cervical carcinoma: DNase I hypersensitivity and methylation of cellular flanking sequences
M. I. Gallego
,
P. Lazo
,
D. Zimonjic
,
N. Popescu
,
J. DiPaolo
Genes, Chromosomes and Cancer
1994
Corpus ID: 46013592
The C4‐1 cell line derived from a non‐keratinizing squamous cell carcinoma of the uterine cervix contains integrated human…
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