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10q22.3
A chromosome band present on 10q
National Institutes of Health
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Related topics
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5 relations
10q
BMPR1A wt Allele
Chromosomes
KCNMA1 wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Ovarian high‐grade endometrioid stromal sarcoma with YWHAE and NUTM2B rearrangements
Noriaki Kikuchi
,
S. Sugita
,
+9 authors
T. Hasegawa
Pathology international (Print)
2017
Corpus ID: 32247382
To the Editor: Here, we present an extremely rare case of primary ovarian high-grade endometrioid stromal sarcoma (OHGESS) with…
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2013
2013
A pilot double-blind, randomized, placebo-controlled trial of curcumin/bioperine for lung cancer chemoprevention in patients with chronic obstructive pulmonary disease
A. Sharafkhaneh
,
J. J. Lee
,
+14 authors
J. Kurie
2013
Corpus ID: 7621308
Chronic obstructive pulmonary disease is an inflammatory condition with increased risk of lung cancer. We hypothesized that…
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2010
2010
Computerized analysis of cytology and fluorescence in situ hybridization (FISH) in induced sputum for lung cancer detection
A. Guber
,
J. Greif
,
+7 authors
M. Daniely
Cancer Cytopathology
2010
Corpus ID: 29007620
Lung cancer results from a multistep process, whereby genetic and epigenetic alterations lead to a malignant phenotype. Somatic…
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2010
2010
Targeted Next-Generation Sequencing and Genome-Wide High-Resolution Copy Number DNA Arrays Allow the Identification of Five Novel RUNX1 Fusions In Hematological Malignancies.
V. Grossmann
,
A. Kohlmann
,
+6 authors
C. Haferlach
2010
Corpus ID: 208463268
Abstract 1193 RUNX1 is a crucial transcription factor involved in cell lineage differentiation during hematopoiesis. It contains…
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2007
2007
A novel locus for autosomal dominant “uncomplicated” hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3
S. Hanein
,
A. Dürr
,
+9 authors
G. Stevanin
Human Genetics
2007
Corpus ID: 10584446
Hereditary spastic paraplegias (HSPs) are genetically and phenotypically heterogeneous. Both “uncomplicated” and “complicated…
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2006
2006
A genome‐wide linkage search for bipolar disorder susceptibility loci in a large and complex pedigree from the eastern part of Cuba
B. Marcheco-Teruel
,
T. Flint
,
+9 authors
O. Mors
American Journal of Medical Genetics Part B…
2006
Corpus ID: 32472771
We present results from a genome‐wide scan of a six generation pedigree with 28 affected members with apparently dominant bipolar…
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2005
2005
Fine mapping of chromosome 10q deletions in mycosis fungoides and sezary syndrome: Identification of two discrete regions of deletion at 10q23.33–24.1 and 10q24.33–25.1
E. Wain
,
T. Mitchell
,
R. Russell‐Jones
,
S. J. Whittaker
Genes, Chromosomes and Cancer
2005
Corpus ID: 34977534
Previous cytogenetic studies in mycosis fungoides (MF) and Sezary syndrome (SS) have identified a large and poorly defined area…
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2002
2002
Analysis of the Human 3’-Phosphoadenosine 5’-Phosphosulfate Synthase Genes
W. G. Campbell
,
K. Venkatachalam
TheScientificWorldJournal
2002
Corpus ID: 49679228
INTRODUCTION. PAPS is the universal sulfonate donor compound. PAPS synthase (PAPSS) catalyzes the formation PAPS in two concerted…
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1998
1998
Assignment1 of the BMPR1A and BMPR1B genes to human chromosome 10q22.3 and 4q23→q24 byin situ hybridization and radiation hybrid map ping
H. Ide
,
F. Saito-Ohara
,
+4 authors
M. Terada
Cytogenetic and Genome Research
1998
Corpus ID: 46751090
Bone morphogenetic proteins (BMPs) are members of the transforming growth factor b superfamily (Wozney, 1992). Three BMP receptor…
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1993
1993
Structure and expression analysis of a member of the human glutamate dehydrogenase (GLUD) gene family mapped to chromosome 10p11.2
G. Tzimagiorgis
,
M. Leversha
,
+4 authors
N. Moschonas
Human Genetics
1993
Corpus ID: 11281695
Glutamate dehydrogenase (GLUD) is a key metabolic enzyme of the mitochondrion, playing an important role in mammalian neuronal…
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