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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 08 Dec 2016.

Forkhead box B1

C43, Foxb1, Mf3, Fkh5, HFH-e5.1
Top mentioned proteins: rad2, CAN, HAD, ACID, Parvalbumin
Papers on C43
Reduction in 50-kHz call-numbers and suppression of tickling-associated positive affective behaviour after lesioning of the lateral hypothalamic parvafox nucleus in rats.
New
Celio et al., Fribourg, Switzerland. In Behav Brain Res, Mar 2016
Its core and shell are composed of neurons expressing the calcium-binding protein parvalbumin (PV) and the transcription factor Foxb1, respectively.
Birthdate of parvalbumin-neurons in the Parvafox-nucleus of the lateral hypothalamus.
New
Celio et al., Fribourg, Switzerland. In Brain Res, Feb 2016
UNASSIGNED: The Parvafox-nucleus in the lateral hypothalamus is characterized by the presence of two distinct neural populations, the Parvalbumin (Parv) and the Foxb1-expressing ones.
The ventrolateral hypothalamic area and the parvafox nucleus: Role in the expression of (positive) emotions?
Review
New
Celio et al., Heidelberg, Germany. In J Comp Neurol, Aug 2015
One promising candidate is the novel parvafox nucleus, which we recently described, in the murine medial forebrain bundle (mfb), which specifically expresses parvalbumin and Foxb1.
Improving furfural tolerance of Zymomonas mobilis by rewiring a sigma factor RpoD protein.
New
He et al., Chengdu, China. In Appl Microbiol Biotechnol, Jun 2015
Three furfural tolerance RpoD mutants (ZM4-MF1, ZM4-MF2, and ZM4-MF3) were identified from error-prone PCR libraries.
LIM homeobox protein 5 (Lhx5) is essential for mamillary body development.
Varela-Echavarría et al., Mexico. In Front Neuroanat, 2014
The MM markers Foxb1, Sim2, and Lhx1 are absent in Lhx5 knock-out mice from early embryonic stages, suggesting abnormal specification of this region.
A genome-wide association study of asthma symptoms in Latin American children.
Barreto et al., Salvador, Brazil. In Bmc Genet, 2014
p-value 2.83 × 10(-8)) and 15q22 region flanking the FOXB1 gene (rs10519031, MAF 0.04, OR 3.0, 95% CI 2.02-4.49,
Cadherins mediate sequential roles through a hierarchy of mechanisms in the developing mammillary body.
Alvarez-Bolado et al., Montréal, Canada. In Front Neuroanat, 2014
We report that, in the Foxb1 mouse mutant, Cdh11 expression fails to be maintained during MBO development.
Effects of dietary fucoidan on the blood constituents, anti-oxidation and innate immunity of juvenile yellow catfish (Pelteobagrus fulvidraco).
Elmada et al., Ningbo, China. In Fish Shellfish Immunol, 2014
The same experimental fish were randomly subjected to one of the following 7 treatments for 12 weeks: The basal diet was applied as control group, the experimental groups were fed on fucoidan extracted from Sargassum horneri (SF) and commodity fucoidan purchased from the market (MF), and the effective dosages were 0.05%, 0.1% and 0.2% per kilogram feed (the groups were respectively marked as SF1, SF2, SF3, MF1, MF2 and MF3).
Halogen bonding: unifying perspectives on organic and inorganic cases.
Donald et al., Richmond, United States. In J Phys Chem A, 2014
We find for distinct classes of halogen bonded complexes (MF3-X···Y) that the ab initio BSSE-corrected binding energies (ΔE) and enthalpies (ΔH) are predicted by functions of the form y = A/r(n) + C.
The effects of two torque values on the screw preload of implant-supported prostheses with passive fit or misfit.
Akeel et al., In Int J Oral Maxillofac Implants, 2014
Four implant-supported frameworks were constructed to represent passive fit (PF) and different amounts of misfit (MF1, MF2, and MF3).
Coaxiality of Foxb1- and parvalbumin-expressing neurons in the lateral hypothalamic PV1-nucleus.
Celio et al., Fribourg, Switzerland. In Neurosci Lett, 2014
During embryogenesis, the ventrolateral hypothalamus is colonized also by Foxb1-expressing neurons.
Genetic mapping of Foxb1-cell lineage shows migration from caudal diencephalon to telencephalon and lateral hypothalamus.
GeneRIF
Alvarez-Bolado et al., Göttingen, Germany. In Eur J Neurosci, 2008
Here we study migrations in the hypothalamic primordium by genetically labeling the Foxb1 diencephalic lineage.
Genetic ablation of the mammillary bodies in the Foxb1 mutant mouse leads to selective deficit of spatial working memory.
GeneRIF
Gruss et al., Göttingen, Germany. In Eur J Neurosci, 2005
Foxb1 mutants showed deficits in the task for spatial navigation within the Barnes maze. Furthermore, they showed impairments in spatial working memory tasks such as the spontaneous alternation and the working memory test in the radial arm maze.
Human FOX gene family (Review).
Review
Katoh et al., Japan. In Int J Oncol, 2004
Human Forkhead-box (FOX) gene family consists of at least 43 members, including FOXA1, FOXA2, FOXA3, FOXB1, FOXC1, FOXC2, FOXD1, FOXD2, FOXD3, FOXD4, FOXD5 (FOXD4L1), FOXD6 (FOXD4L3), FOXE1, FOXE2, FOXE3, FOXF1, FOXF2, FOXG1 (FOXG1B), FOXH1, FOXI1, FOXJ1, FOXJ2, FOXJ3, FOXK1, FOXK2, FOXL1, FOXL2, FOXM1, FOXN1, FOXN2 (HTLF), FOXN3 (CHES1), FOXN4, FOXN5 (FOXR1), FOXN6 (FOXR2), FOXO1 (FOXO1A), FOXO2 (FOXO6), FOXO3 (FOXO3A), FOXO4 (MLLT7), FOXP1, FOXP2, FOXP3, FOXP4, and FOXQ1.
Diagnosis, pathogenesis and treatment of the myeloproliferative disorders essential thrombocythemia, polycythemia vera and essential megakaryocytic granulocytic metaplasia and myelofibrosis.
Review
Thiele et al., Amsterdam, Netherlands. In Neth J Med, 1999
Myelofibrosis in ET, PV and EMGM is graded into: no reticulin fibrosis (MF0), early reticulin fibrosis (MF1), advanced reticulin sclerosis with minor or moderate collagen fibrosis (MF2) and advanced collagen fibrosis with osteosclerosis (MF3).
Diagnostic criteria of the myeloproliferative disorders (MPD): essential thrombocythaemia, polycythaemia vera and chronic megakaryocytic granulocytic metaplasia.
Review
Michiels, Netherlands. In Neth J Med, 1997
Myelofibrosis in ET, PV and CMGM is graded in no reticulin fibrosis (MFO), early reticulin fibrosis (MF1), advanced reticulin sclerosis with minor collagen fibrosis (MF2) and advanced collagen fibrosis with or without osteosclerosis (MF3).
The genetic control of cell proliferation in Drosophila imaginal discs.
Review
Schmidt et al., Irvine, United States. In J Cell Sci Suppl, 1989
In some of these mutants (fat, lgd, c43, dco) the overgrowing tissue is hyperplastic; it retains its single-layered epithelial structure and is capable of differentiating.
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