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PHLDB1 gene
Known as:
pleckstrin homology like domain family B member 1
, FLJ00141
, PHLDB1
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National Institutes of Health
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PHLDA1 gene
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Role of polymorphisms of FAM13A, PHLDB1, and CYP24A1 in breast cancer risk.
Ying Wei
,
Xiaolin Wang
,
+4 authors
Xinhan Zhao
Current molecular medicine
2019
Corpus ID: 195067751
BACKGROUND Single-nucleotide polymorphisms (SNPs) are important indicators of susceptibility to breast cancer. OBJECTIVE To…
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2019
2019
A PHLDB1 variant associated with the nonfunctional pituitary adenoma
L. Kim
,
Jeong-Hyun Kim
,
+7 authors
H. Shin
Journal of Neuro-Oncology
2019
Corpus ID: 76661064
PurposePrevious studies have revealed that PHLDB1 single-nucleotide polymorphisms (SNPs) are associated with glioma risk…
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2017
2017
Pleckstrin homology-like domain family B member 1 rs498872 polymorphism and glioma risk in Chinese Han population.
J.-W. Zhang
,
Z.H. Liu
,
X. Lin
,
Yanqun Du
,
H. Guo
Cellular and Molecular Biology
2017
Corpus ID: 20851343
This case-control study aimed to investigate the association between PHLDB1 rs498872 polymorphism and the risk of glioma in a…
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Review
2015
Review
2015
The PHLDB1 rs498872 (11q23.3) polymorphism and glioma risk: A meta‐analysis
Xingchun Gao
,
Yajing Mi
,
+6 authors
Xingchun Gou
Asia-Pacific Journal of Clinical Oncology
2015
Corpus ID: 12937086
The association between the rs498872 single nucleotide polymorphism (SNP) and glioma risk has been studied, but these studies…
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2011
2011
With Glioma Susceptibility in a Chinese Population
Hongyan Chen
,
Yuanyuan Chen
,
+8 authors
D. Lu
2011
Corpus ID: 18413940
Two genome-wide association studies of glioma in European populations identified 14 genetic variants strongly associated with…
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2010
2010
Clinical Cancer esearch ing , Diagnosis , Prognosis etic Risk Profiles Identify Different R ecular Etiologies for Glioma
M. Mark
,
ias Simon
,
+13 authors
M. Sanson
2010
Corpus ID: 673647
Download pose: Genome-wide association studies have recently identified single-nucleotide polymorphisms in five loci at 5p15.33…
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2004
2004
Germ-line mutation of Foxn5 gene in mouse lineage.
Masuko Katoh
,
M. Katoh
International Journal of Molecular Medicine
2004
Corpus ID: 19542566
Amplified region (amplicon) around MLL gene is closely linked to the 11q23.3 commonly deleted region of neuroblastoma, which…
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2004
2004
Identification and characterization of human FOXN5 and rat Foxn5 genes in silico.
Masuko Katoh
,
M. Katoh
International Journal of Oncology
2004
Corpus ID: 10679761
Forkhead-box (FOX) genes are implicated in embryogenesis through transcriptional regulation depending on SHH-GLI pathway, TGF…
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