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searching for PHOX2B 4 found (14 total)

alternate case: pHOX2B

Stanislas Lyonnet (884 words) [view diff] exact match in snippet view article find links to article

Polyalanine expansion and frame shift mutations of the paired-lik homeobox gene PHOX2B in congenital central hypoventilation syndrome (Ondine’s curse). Nat Genet

HSD2 neuron (1,828 words) [view diff] case mismatch in snippet view article find links to article

factor Phox2b. This means that HSD2 neurons probably release the excitatory transmitter glutamate onto their synaptic target neurons, as all Phox2b-expressing

ROHHAD (2,932 words) [view diff] exact match in snippet view article find links to article

differentiated from one other, as patients with CCHS have mutations in the PHOX2B gene, whereas ROHHAD patients do not. The ROHHAD Association is an organization

List of human transcription factors (81 words) [view diff] exact match in snippet view article find links to article

ENSG00000165462 Homeodomain Known motif – High-throughput in vitro [696] TAATTRVRTTA PHOX2B ENSG00000109132 Homeodomain Known motif – High-throughput in vitro [697]