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This is the first report to describe genome-wide Lmx1b binding during limb development.
Otx2 (zeige OTX2 ELISA Kits) critically depends on Lmx1b for the formation of mdDA neurons.
results demonstrate an important role for the intersection of Lmx1b and Hoxb8 (zeige HOXB8 ELISA Kits)::cre expression in the development of nociceptive dorsal horn circuits critical for mechanical and thermal pain processing.
Co-immunoprecipitation experiments show that both wild-type and Icst LMX1B are found in complexes with LIM domain binding protein 1 (LDB1 (zeige LDB1 ELISA Kits)), resulting in lower levels of functional LMX1B in Icst heterozygotes than null heterozygotes
We posit that microRNA modulation of the Lmx1b/Wnt (zeige WNT2 ELISA Kits) axis in the early midbrain/isthmus could determine midbrain size and allocation of dopamine progenitors.
Cell biological and biophysical experiments with primary podocytes isolated after 1 week of Lmx1b inactivation indicated dysregulation of actin cytoskeleton organization
Lmx1b, a key transcription factor for the specification of 5-HT (zeige DDC ELISA Kits) and dopaminergic transmitter phenotypes during embryogenesis, determines some peptide phenotypes in these neurons as well.
Data indicate that tryptophan hydroxylase 2 Tph2 (zeige TPH2 ELISA Kits)-/- and LIM homeobox transcription factor 1 beta Lmx1b-/- females displayed a change in sexual preference.
A protein complex was identified containing PSPC1 (zeige PSPC1 ELISA Kits), PSF (zeige IL-3 ELISA Kits) and LMX1B, suggesting the existence of this complex in mesodiencephalic dopaminergic neurons.
Lmx1b genes are associated with skeletal development.
9q33.3q34.11 microdeletion including LMX1b gene identified in four patients with intellectual disability, epilepsy, nail (zeige CD244 ELISA Kits) dysplasia and bone malformations.
Report progression of autosomal dominant renal-limited disease with LMX1B mutation.
38 different LMX1B polymorphisms have been found in 55 families with Nail (zeige CD244 ELISA Kits)-Patella Syndrome raising the hypothesis of a genetic heterogeneity.
Lmx1a (zeige LMX1A ELISA Kits) and Lmx1b expression persists in mature dopaminergic neurons of the substantia nigra pars (zeige EPRS ELISA Kits) compacta and the ventral tegmental area. [Review]
these results reveal a sustained and essential requirement of Lmx1b for the function of midbrain dopamine neurons
A heterozygous microdeletion of the entire LMX1B gene using multiplex ligation-dependent probe amplification (MLPA) in a Chinese family with nail (zeige CD244 ELISA Kits) patella syndrome, is reported.
Results demonstrate that loss of function may not be the only way that mutated LMX1b causes haploinsufficiency. Mutated LMX1b may interfere withdownsteam transcription events.
In a large family with the two disorders with two novel frameshift TSC1 (zeige TSC1 ELISA Kits) and LMX1B mutations, we describe the phenotypes
LMX1B is a novel oncogene (zeige RAB1A ELISA Kits) in ovarian cancer pathogenesis.
this study identified two novel mutations of the LMX1B gene in three unrelated families with autosomaldominant Focal Segmental Glomerulosclerosis and no extrarenal features.
Lmx1ba and Lmx1bb function at least partially redundantly in the spinal cord and three functional lmx1b alleles are required in zebrafish for correct numbers of excitatory spinal interneurons at later developmental stages.
Lmx1b and FoxC have roles in regulating podocin expression in podocytes
lmx1b paralogues may contribute to the generation of diencephalic dopaminergic precursors
Results suggest that zebrafish lmx1b.1 and lmx1b.2 promote the survival of periocular mesenchymal cells that influence multiple signaling events required for proper ocular development.
Imx1b.1 regulation of wnt (zeige WNT2 ELISA Kits) proteins, pax8 (zeige PAX8 ELISA Kits) and fibroblast growth factor 8 (fgf8 (zeige FGF8 ELISA Kits)) maintains cell survival in the isthmocerebellar region
The spontaneous calcium spike activity in the hindbrain of developing Xenopus laevis larvae modulates the specification of serotonergic neurons via regulation of expression of the Lmx1b transcription factor.
We have over-expressed lmx1b mRNA alone or in combination with potential interacting molecules and analysed the effects on embryonic kidney structures.
This gene encodes a member of LIM-homeodomain family of proteins containing two N-terminal zinc-binding LIM domains, 1 homeodomain, and a C-terminal glutamine-rich domain. It functions as a transcription factor, and is essential for the normal development of dorsal limb structures, the glomerular basement membrane, the anterior segment of the eye, and dopaminergic and serotonergic neurons. Mutations in this gene are associated with nail-patella syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
LIM homeobox transcription factor 1, beta
, LIM homeo box transcription factor 1B
, LIM homeobox transcription factor 1-beta
, LIM/homeobox protein 1.2
, LIM/homeobox protein LMX1B
, LIM homeobox protein
, LIM/homeobox protein 1
, LIM/homeobox protein LMX-1.2
, homeobox protein LMX-1
, homeodomain protein (lmx)
, LIM homeobox transcription factor 1, beta 1
, LIM homeobox protein 1b
, LIM homeobox transcription factor 1-beta.1