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searching for PAX7 10 found (38 total)

alternate case: pAX7

List of MeSH codes (D12.776.260) (972 words) [view diff] no match in snippet view article

The following is a partial list of the "D" codes for Medical Subject Headings (MeSH), as defined by the United States National Library of Medicine (NLM)

Hard palate (980 words) [view diff] exact match in snippet view article find links to article

several genetic risk factors. Six single-nucleotide polymorphisms in the PAX7 gene are implicated in the development of facial features. These variations

Trunk neural crest (271 words) [view diff] case mismatch in snippet view article find links to article

Sarasa M; Domínguez L (August 2005). "Novel expression patterns of Pax3/Pax7 in early trunk neural crest and its melanocyte and non-melanocyte lineages

Margaret Buckingham (1,578 words) [view diff] case mismatch in snippet view article find links to article

onset of myogenesis in the embryo. They discovered a population of Pax3/Pax7-positive progenitors that are essential for foetal muscle development and

Embryonal rhabdomyosarcoma (3,762 words) [view diff] exact match in snippet view article find links to article

Embryonal rhabdomyosarcoma can be classified by its lack of PAX3–FOXO1 or PAX7–FOXO1 gene fusions, but approximately 20% of alveolar rhabdomyosarcomas are

PAXBP1 (550 words) [view diff] exact match in snippet view article find links to article

Identifiers Aliases PAXBP1, BM020, C21orf66, FSAP105, GCFC, GCFC1, PAX3 and PAX7 binding protein 1 External IDs OMIM: 617621; MGI: 1914617; HomoloGene: 9604;

Mir-1 microRNA precursor family (3,291 words) [view diff] case mismatch in snippet view article find links to article

skeletal muscle satellite cell proliferation and differentiation by repressing Pax7". The Journal of Cell Biology. 190 (5): 867–79. doi:10.1083/jcb.200911036

Ohad Birk (3,396 words) [view diff] exact match in snippet view article find links to article

mutation A syndrome of hypotonia and global neurodevelopmental delay caused by PAX7 mutation. Intellectual disability syndrome caused by RSRC1 mutation, causing

Sonic hedgehog protein (7,266 words) [view diff] case mismatch in snippet view article find links to article

transcription factors—Nkx2.2, Olig2, Nkx6.1, Nkx6.2, Dbx1, Dbx2, Irx3, Pax6, and Pax7—that is regulated by the SHH gradient. These transcription factors are induced

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

Paired box Known motif – High-throughput in vitro [679] YACGCHYSRNYRMNY PAX7 ENSG00000009709 Homeodomain; Paired box Known motif – High-throughput in