Results 71 to 80 of about 14,972 (184)
Chemotherapy Effectiveness and Prognosis of Gastric Cancer Influenced by PTPN11 Polymorphisms
Objective: Since gastric cancer (GC) cells exhibited higher grades of SHP-2 encoded by PTPN11 than normal cells, it would be intriguing to explore whether PTPN11 single nucleotide polymorphisms (SNPs) would influence chemotherapy effectiveness and GC ...
Chuanjun Zhuo +9 more
doaj +1 more source
ABSTRACT Noonan syndrome (NS) is a genetically heterogeneous disorder characterized by a broad spectrum of clinical features resulting from dysregulation of the RAS/MAPK pathway. Although complex genotypes are increasingly recognized in NS, cases harboring two distinct pathogenic variants in different NS genes remain extremely rare.
Francesco Prevedello +10 more
wiley +1 more source
The graphical abstract illustrates the action mechanisms through which PPE alleviates HUA by inhibiting XOD activity, and by suppressing the PI3K‐AKT signaling pathway to downregulate the expression of the urate reabsorption transporters URAT1 and GLUT9, thereby promoting renal UA excretion and attenuating renal injury.
Zeyu Yin +6 more
wiley +1 more source
PTPN11 in cartilage development, adult homeostasis, and diseases
Abstract The SH2 domain-containing protein tyrosine phosphatase 2 (SHP2, also known as PTP2C), encoded by PTPN11, is ubiquitously expressed and has context-specific effects. It promotes RAS/MAPK signaling downstream of receptor tyrosine kinases, cytokine receptors, and extracellular matrix proteins, and was shown in various lineages to ...
Wentian Yang, Véronique Lefebvre
openaire +3 more sources
Stunted growth remains a critical public health concern, particularly in developing regions. This study investigates the potential of active compounds derived from Sauropus androgynus as dietary supplements for preventing growth stunting, employing a ...
Arwansyah Arwansyah +6 more
doaj +1 more source
Noonan syndrome with multiple lentigines (NSML), formerly known as LEOPARD Syndrome, is a rare autosomal dominant disorder. Approximately 90% of NSML cases are caused by missense mutations in the PTPN11 gene which encodes the protein tyrosine phosphatase
Rong Li +10 more
doaj +1 more source
A Novel A461S Mutation of PTPN11 in a Female with LEOPARD Syndrome
LEOPARD syndrome (LS) is a congenital developmental disorder and is an acronym for multiple lentigines, electrocardiographic conduction abnormalities, ocular hypertelorism, pulmonary stenosis, abnormalities of genitalia, retardation of growth, and sensorineural deafness (1).
Yoshida, Rie, Ogata, Tsutomu
openaire +3 more sources
TNO155 is a selective SHP2 inhibitor to target PTPN11-dependent oral squamous cell carcinoma
Oral squamous cell carcinoma (OSCC) is known to be driven by multiple intricated receptor tyrosine kinases (RTKs) including EGFR, PI3K/AKT and MAPK signaling pathways.
Annie Wai Yeeng Chai +5 more
doaj +1 more source
American Journal of Hematology, Volume 101, Issue 8, Page 2038-2043, August 2026.
Sankalp Arora +18 more
wiley +1 more source
Background Noonan syndrome has a wide range of symptoms due to dysregulation of the RAS/MAPK pathway with several gene variations, including the PTPN11 gene. There are currently no case reports of Noonan syndrome with eosinophilic gastroenteritis. Case A
Nobuhiko Koga +5 more
doaj +1 more source

