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Paired Mesoderm Homeobox Protein 2B
Known as:
PHOX2B Homeodomain Protein
, Paired-Like Homeobox 2B
, Neuroblastoma Phox
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Paired mesoderm homeobox protein 2B (314 aa, ~32 kDa) is encoded by the human PHOX2B gene. This protein plays a role in the regulation of gene…
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National Institutes of Health
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Related topics
Related topics
8 relations
DNA-Binding Proteins
Genes, Regulator
Homeodomain Proteins
PHOX2B gene
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Screening Children with a Family History of Central Congenital Hypoventilation Syndrome
H. Emanuel
,
Kimberly M. Rennie
,
Kelly T. Macdonald
,
A. Yadav
,
R. Mosquera
Case Reports in Pediatrics
2020
Corpus ID: 215537115
Congenital central hypoventilation syndrome (CCHS) is a rare genetic disorder of an autonomic nervous disorder that affects…
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2019
2019
Analysis of the neuronal network of the medullary respiratory center in transgenic rats expressing archaerhodopsin-3 in Phox2b-expressing cells
K. Ikeda
,
R. Kaneko
,
+5 authors
H. Onimaru
Brain Research Bulletin
2019
Corpus ID: 53434625
2019
2019
A Novel c.676_677insG PHOX2B Mutation in Congenital Central Hypoventilation Syndrome.
Guodong Ye
,
Daxiong Han
,
+8 authors
Qiwei Guo
Journal of clinical sleep medicine : JCSM…
2019
Corpus ID: 73727423
ABSTRACT Paired-like homeobox (PHOX)2B is considered to be the causative gene of congenital central hypoventilation syndrome…
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Review
2014
Review
2014
Cytoarchitecture and CO(2) sensitivity of Phox2b-positive Parafacial neurons in the newborn rat medulla.
H. Onimaru
,
K. Ikeda
,
Tani Mariho
,
K. Kawakami
Progress in Brain Research
2014
Corpus ID: 21367352
2013
2013
Several Cis-regulatory Elements Control mRNA Stability, Translation Efficiency, and Expression Pattern of Prrxl1 (Paired Related Homeobox Protein-like 1)*
I. Regadas
,
M. Matos
,
+5 authors
C. Reguenga
Journal of Biological Chemistry
2013
Corpus ID: 23922425
Background: The mechanisms that control the Prrxl1 expression are poorly understood. Results: Several regulatory elements present…
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2011
2011
Spatial and temporal mechanisms of cell fate determination in the developing CNS
José M. Dias
2011
Corpus ID: 53572833
The generation of neural cell diversity in the developing central nervous system relies on mechanisms that provide spatial and…
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2007
2007
De novo polyalanine expansion of PHOX2B in congenital central hypoventilation syndrome: unequal sister chromatid exchange during paternal gametogenesis
H. Arai
,
T. Otagiri
,
+4 authors
K. Hayasaka
Journal of Human Genetics
2007
Corpus ID: 23475661
AbstractThe expansion of polyalanine repeats is known to cause at least nine disorders, including congenital central…
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2004
2004
Haploinsufficiency for Phox 2 b in mice causes dilated pupils and atrophy of the ciliary ganglion : mechanistic insights into human congenital central hypoventilation syndrome
S. Cross
,
J. Morgan
,
+6 authors
I. Jackson
2004
Corpus ID: 108285413
Dilp1 is a semi-dominant mouse mutation that causes dilated pupils when heterozygous and is lethal when homozygous. We report…
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Highly Cited
2000
Highly Cited
2000
Paired-like homeodomain proteins Phox2a/Arix and Phox2b/NBPhox have similar genetic organization and independently regulate dopamine beta-hydroxylase gene transcription.
Megumi Adachi
,
David Browne
,
Elaine J. Lewis
DNA and Cell Biology
2000
Corpus ID: 45363092
The homeodomain transcription factors Arix/Phox2a and NBPhox/Phox2b play a role in the specification of the noradrenergic…
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1999
1999
Genomic structure and functional characterization of NBPhox (PMX2B), a homeodomain protein specific to catecholaminergic cells that is involved in second messenger-mediated transcriptional activation…
M. Yokoyama
,
H. Watanabe
,
M. Nakamura
Genomics
1999
Corpus ID: 25848773
Homeodomain proteins play essential roles in basic processes during embryogenesis and development. NBPhox, a vertebrate paired…
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