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searching for PTPN11 8 found (55 total)

alternate case: pTPN11

TREML1 (602 words) [view diff] exact match in snippet view article find links to article

and functional properties. TREML1 enhances calcium signaling in an SHP2 (PTPN11; MIM 176876)-dependent manner (Allcock et al., 2003; Barrow et al., 2004)

MIR489 (557 words) [view diff] exact match in snippet view article find links to article

Okamoto Y, Seki N (2010). "miR-489 is a tumour-suppressive miRNA target PTPN11 in hypopharyngeal squamous cell carcinoma (HSCC)". Br. J. Cancer. 103 (6):

List of genes mutated in cutaneous conditions (108 words) [view diff] exact match in snippet view article find links to article

basal cell carcinoma PTEN Bannayan–Riley–Ruvalcaba syndrome Cowden syndrome PTPN11 LEOPARD syndrome RAB27A Griscelli syndrome RAG1 Severe combined immunodeficiency

Central giant-cell granuloma (775 words) [view diff] exact match in snippet view article find links to article

Multiple CGCGs can be found in individuals with Noonan syndrome. Mutations in PTPN11 or RAS pathway genes are seen. Radiographically, CGCGs have a rounded cyst-like

Mir-489 microRNA precursor family (434 words) [view diff] exact match in snippet view article find links to article

Seki N (September 2010). "miR-489 is a tumour-suppressive miRNA target PTPN11 in hypopharyngeal squamous cell carcinoma (HSCC)". British Journal of Cancer

Germline mosaicism (1,435 words) [view diff] exact match in snippet view article find links to article

genetic testing revealing that both of the siblings with NS share the same PTPN11 haplotype from both parents, while a distinct paternal and maternal haplotype

Gary Firestein (1,188 words) [view diff] exact match in snippet view article find links to article

Vida; Boyle, David L.; Muench, German R. Aleman (2016-05-19). "Abnormal PTPN11 enhancer methylation promotes rheumatoid arthritis fibroblast-like synoviocyte

Coiled-coil domain containing 42B (2,150 words) [view diff] exact match in snippet view article find links to article

is linked Noonan syndrome 1 that is caused by heterozygote mutation in PTPN11 gene product, SH-PTP2, and primarily causing facial developmental defects