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searching for STK11 9 found (329 total)

alternate case: sTK11

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

syndrome SPREAD1 Neurofibromatosis type 1-like syndrome STK11 Peutz–Jeghers syndrome TERC Dyskeratosis congenita TGM1 Transglutaminase

Negrito (2,016 words) [view diff] exact match in snippet view article find links to article

convergence driven by admixture (e.g., MTHFD1 and RAD18), new mutations (e.g., STK11), or notably purifying selection (e.g., MC1R). Endicott, Phillip; Gilbert

TUSC3 (638 words) [view diff] exact match in snippet view article find links to article

S2CID 26030376. Guervós MA, Marcos CA, Hermsen M, et al. (2007). "Deletions of N33, STK11 and TP53 are involved in the development of lymph node metastasis in larynx

Fibroblast growth factor 21 (3,036 words) [view diff] exact match in snippet view article find links to article

of FGF21 on mitochondrial function require serine/threonine kinase 11 (STK11/LKB1), which activates AMPK. Inhibition of AMPK, SIRT1, and PGC-1α activities

Hepatocellular carcinoma (9,631 words) [view diff] exact match in snippet view article find links to article

Nagaraju, Ganji Purnachandra; Vadde, Ramakrishna (eds.), "Chapter 22 - LKB1/STK11-mediated signal transduction in hepatocellular carcinoma", Theranostics

Cancer epigenetics (12,530 words) [view diff] exact match in snippet view article find links to article

Most cases of lung cancer are because of genetic mutations in EGFR, KRAS, STK11 (also known as LKB1), TP53 (also known as p53), and CDKN2A (also known as

Research in multiple sclerosis (7,886 words) [view diff] exact match in snippet view article find links to article

mutations have been associated with an increased risk to develop MS, like STK11-SNP. The chronic demyelination may cause axons to be notably vulnerable

Peter Fecci (2,318 words) [view diff] exact match in snippet view article find links to article

(2016) S Koyama, EA Akbay, YY Li, AR Aref, F Skoulidis, GS Herter-Sprie: STK11/LKB1 deficiency promotes neutrophil recruitment and proinflammatory cytokine

Yuri Nikiforov (scientist) (2,537 words) [view diff] exact match in snippet view article

Y, Witchel S. Identification of unique heterozygous germline mutation, STK11 (p.F354L), in a child with encapsulated follicular variant of papillary