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PITX3 encodes a member of the RIEG/PITX homeobox family, which is in the bicoid class of homeodomain proteins. Additionally we are shipping Pituitary Homeobox 3 Proteins (8) and many more products for this protein.
Showing 10 out of 40 products:
Cow (Bovine) Polyclonal PITX3 Primary Antibody for WB - ABIN2780637
Bidinost, Hernandez, Edward, Al-Rajhi, Lewis, Lupski, Stockton, Bejjani: Of mice and men: tyrosinase modification of congenital glaucoma in mice but not in humans. in Investigative ophthalmology & visual science 2006
Show all 2 references for ABIN2780637
Human Polyclonal PITX3 Primary Antibody for EIA, WB - ABIN375225
Kim, Inoue, Ishii, Vanti, Voronov, Murchison, Hannon, Abeliovich: A MicroRNA feedback circuit in midbrain dopamine neurons. in Science (New York, N.Y.) 2007
novel PITX3 mutation c.573del, p.(Ser192Alafs*117), was identified in heterozygous state in a Belgo-Romanian family with a similar phenotype
our data demonstrate that key midbrain dopamine regulators (Nurr1 (show NR4A2 Antibodies), Pitx3, and Lmx1a (show LMX1A Antibodies)) play overlapping as well as distinct roles during neurogenesis and neurotransmitter phenotype determination of mDA neurons
Mutations in PITX3 are not a common cause or a risk factor for multisystem atrophy and progressive supranuclear palsy in the Polish population.
Presence of the rs4919621 allele A in PITX3 significantly increases the risk of Parkinson's disease (PD) patients in a Caucasian population, while rs2281983 allele C and rs4919621 allele A were both risk factors in early onset PD.
This study provided that NURR1 (show NR4A2 Antibodies) and PITX3 gene expression is decreased in the peripheral blood lymphocytes of Chinese patients with Parkinson's disease patients.
novel synonymous SNP in PITX3 gene may contribute to PD risk in the Chinese population.
Deletion of PITX3 is associated with aggressive neurobehavioral phenotype in Smith-Magenis Syndrome.
Data show that BFSP2 (show BFSP2 Antibodies) and PITX3, hitherto known to cause eye defects only in a dominant fashion, can also present recessively.
The results of this study suggested that these PITX3 SNPs do not contribute to the risk of developing PD in EOPD or LOPD in Chinese.
The single nucleotide polymorphism rs3758549 (C >T substitution) in the Pitx3 gene is a potential risk for sporadic Parkinson disease (PD), especially early-onset PD in Chinese Han population.
In Xenopus, pitx3 appears to inhibit the rotation of presomitic cell cohorts and to be necessary to the bilaterally symmetric expression of pitx2 (show PITX2 Antibodies) in somites.
Microarray-based identification of Pitx3 targets during Xenopus embryogenesis.
expression of Pitx3 in the presumptive lens ectoderm is critical for retina development
Pitx3 is specifically required for DA-related function and, if impaired, Pitx3 could contribute during the pathogenesis of Parkinson's disease.
the sonic hedgehog (show SHH Antibodies) signaling pathway is both necessary and sufficient for the induction of ectopic PITX3 expression in chick mesencephalon downstream of WNT9A (show WNT9A Antibodies)-induced LMX1a (show LMX1A Antibodies) transcription.
microphthalmos/aphakia inPITX3 nonsense mutant is caused by the expression of truncated PITX3, resulting in the abnormal expression of downstream targets and lens fiber proteins.
Pitx3 binds to an evolutionary conserved bicoid-binding site on the 5'-upstream region of Foxe3 (show FOXE3 Antibodies). Pitx3 binding to 5'-upstream region of Foxe3 (show FOXE3 Antibodies) increased transcriptional activity significantly in a cell-based reporter assay.
During fetal myogenesis, Pitx2 (show PITX2 Antibodies)/3 control this redox state through the regulation of Nrf1 (show NRF1 Antibodies) and of antioxidant pathways.
Pitx3 overexpressing mouse significantly affects the gene expression of midbrain dopamine neurons. Motor coordination and locomotion activities are significantly affected in mice overexpressing Pitx3 mice.
Primary fetal neurobehavioral deficit of the Pitx3 mutation is akinesia related to nigrostriatal damage.
Two crucial mediators of mesodiencephalic dopaminergic neuronal development, En1 (show EN1 Antibodies) and Pitx3, interact in dopaminergic subset specification.
a novel link between Pitx3 function and the selective pattern of midbrain dopaminergic neurons cell loss observed in Parkinson's disease.
Reduced Th expression was associated with loss of Pitx3.
pitx3 expression in the primordia of the pituitary, lens, olfactory mucosa, and cranial ganglia is modulated by hedgehog (show SHH Antibodies) and nodal proteins' signaling.
results demonstrate zebrafish pitx3 represents a true ortholog of the human PITX3 gene and the general function of the Pitx3 protein in lens development is conserved between mammals and the teleost fish
Data demonstrate that Foxe3 (show FOXE3 Antibodies) is necessary for lens development in zebrafish and that foxe3 (show FOXE3 Antibodies) lies genetically downstream of pitx3 in a zebrafish lens development pathway.
while lmx1b (show LMX1B Antibodies) paralogues may contribute to the generation of diencephalic dopaminergic precursors. Conversely, knock-down of pitx3 does not specifically affect any diencephalic dopamine cluster
This gene encodes a member of the RIEG/PITX homeobox family, which is in the bicoid class of homeodomain proteins. Members of this family act as transcription factors. This protein is involved in lens formation during eye development. Mutations of this gene have been associated with anterior segment mesenchymal dysgenesis and congenital cataracts.
pituitary homeobox 3
, homeobox protein PITX3
, paired-like homeodomain transcription factor 3
, homeobox protein PTX3
, homeodomain transcription factor Pitx-3
, Pituitary homeobox 3 (Homeobox protein PITX3)
, bicoid-like homeodomain transcription factor 3
, bicoid-like homeodomain transcription factor Pitx3