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LMX1B gene

Known as: LIM Homeobox Transcription Factor 1, Beta Gene, LIM HOMEOBOX TRANSCRIPTION FACTOR 1, BETA, LMX1B 
This gene plays a role in both transcriptional regulation and the mediation of limb development.
National Institutes of Health

Related topics

Related topics

8 relations
Cell Differentiation processHomo sapiensLIM homeobox transcription factor 1 betaLimb Development

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LMX1B wt Allele

Papers overview

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2017
2017
A familial case of nail patella syndrome with a heterozygous in-frame indel mutation in the LIM domain of LMX1B.
2014
2014
LIM homeobox transcription factor 1B expression affects renal interstitial fibrosis and apoptosis in unilateral ureteral obstructed rats.
LIM homeobox transcription factor 1B (LMX1B) is a transcription factor of the LIM homeodomain type and has been implicated in the… 
2013
2013
Lmx1b controls peptide phenotypes in serotonergic and dopaminergic neurons.
Serotonin (5-HT) neurons synthesize a variety of peptides. How these peptides are controlled during development remains unclear… 
2011
2011
c.194 A>C (Q65P) mutation in the LMX1B gene in patients with nail-patella syndrome associated with glaucoma
Purpose To report the clinical, ophthalmic, extraophthalmic, and genetic characteristics of nail-patella syndrome (NPS) in a… 
2011
2011
LMX1B gene mutation in a Saudi patient with bilateral symmetrical hypoplastic nails of the hands
Nail-patella syndrome (NPS) is a rare autosomal dominant disorder that is highly penetrant with marked phonotypical variability… 
2009
2009
A Synonymous Genetic Alteration of LMX1B in a Family with Nail-Patella Syndrome
The gene responsible for nail-patella syndrome, LMX1B, has recently been identified on chromosome 9q. Here we present a patient… 
2004
2004
Characterization of migration behavior of myogenic precursor cells in the limb bud with respect to Lmx1b expression
Limb buds develop from lateral plate-derived stationary mesenchyme and are invaded by cells from extrinsic regions. The largest… 
Review
2003
Review
2003
[From gene to disease; the nail-patella syndrome and the LMX1B gene].
Nail-patella syndrome (NPS) is an autosomal dominant hereditary disorder characterised by nail dysplasia, patellar apoplasia… 
2003
2003
LMX1B 17-bp Deletion and A3243G mtDNA Transition in a Previously Described Patient
Recently, we described a 45-year-old man with the typical phenotypic features of nail-patella syndrome (NPS, dysplastic nails… 
2002
2002
Meier-Gorlin syndrome (ear-patella-short stature syndrome) in an Italian patient: clinical evaluation and analysis of possible candidate genes.
We report on an Italian boy with the Meier-Gorlin syndrome (ear-patella-short stature syndrome). This rare autosomal recessive… 
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