Ladybird Homeobox 1 Proteins (Lbx1)

Human Ladybird Homeobox 1 (Lbx1) interaction partners

1. Homozygous LBX1 Frameshift Mutation Causes Recessive Congenital Central Hypoventilation Syndrome.

2. Two single nucleotide polymorphisms around LBX1 are associated with adolescent idiopathic scoliosis in a Northern Chinese Han population.

3. Meta-analysis provides evidence that rs111090870, rs678741 and rs625039 polymorphisms near LBX1 gene are associated with adolescent idiopathic scoliosis susceptibility in some populations.[meta-analysis]

4. LBX1 is a susceptibility gene for idiopathic scoliosis in a Scandinavian population.

5. In embryos overexpressing lbx1b, wnt5b, a ligand of the non-canonical Wnt/planar cell polarity (PCP) pathway, was significantly downregulated.

6. Our results identify two clinically relevant haplotypes in the LBX1-region with opposite effects on AIS risk.

7. Based on meta-analysis rs11190870 near LBX1 is likely a susceptibility variant for adolescent idiopathic scoliosis in East Asians.

8. Performed a meta-analysis of the LBX1 locus in six Asian and three non-Asian cohorts of adolescent idiopathic scoliosis (AIS) and found significant evidence for association of this locus with AIS susceptibility in all nine cohorts.

9. The SNP rs11190870 near LBX1 is associated with both susceptibility and curve progression of adolescent idiopathic scoliosis in Han Chinese adolescents.

10. This study shows that the genetic variants near the LBX1 gene are associated with adolescent idiopathic scoliosis susceptibility in Chinese Han population.

11. Single nucleotide polymorphism near LBX1 is significantly associated with adolescent idiopathic scoliosis in southern Chinese.

12. A genome-wide association study identifies common variants near LBX1 associated with adolescent idiopathic scoliosis

13. Ladybird homeobox 1 (LBX1), a developmentally regulated homeobox gene, directs expression of the known EMT inducers ZEB1, ZEB2, Snail1, and transforming growth factor beta2 (TGFB2).

Pig (Porcine) Ladybird Homeobox 1 (Lbx1) interaction partners

1. Lbx1 gene might be a candidate gene of carcass traits and provide useful information for further studies on its roles in porcine skeletal muscle.

Mouse (Murine) Ladybird Homeobox 1 (Lbx1) interaction partners

1. Loss of LBX1 gene is associated with Hypoventilation.

2. Chmp2b is one of the most highly regulated cell-autonomous targets of Lbx1 in the embryonic mouse neural tube

3. Lbx1 is expressed in and required for the correct specification of three early dorsal interneuron populations and late-born neurons that form the substantia gelatinosa. Lbx1 plays a critical role in the development of sensory pathways in the spinal cord.

4. Lbx1 is required for correct dorsal-ventral patterning of the neural tube. Lbx1/Pax3 double-mutant mice showed a completely open neural tube.

5. Inactivation of the Lbx1 gene in mice resulted in defects in heart looping, changes in gene expression pattern, and increased cell division; Pax3 and Lbx1 participate in negative regulatory feedback

6. Corl1 interacted with Lbx1 and cooperatively repressed transcription, suggesting that it acts as a transcriptional corepressor for Lbx1 in regulating cell fate determination in the dorsal spinal cord.

7. Lbx1 and Tlx3 are opposing switches in determining GABAergic versus glutamatergic transmitter phenotypes.

8. Homeobox gene Lbx1 is essential for imposing a somatosensory fate on relay neurons in the hindbrain.

9. Functional analysis of homeodomain-containing transcription factor Lbx1 in satellite cells of mouse skeletal muscle is reported.

10. The respiratory rhythm generation within the pre-Botzinger complex (preBotC) is presumably functional in Lbx1 mutant mice with additional neurochemical drive.