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Mirror syndrome and placental ectopic liver in association with de novo SOS1 ...

Tanaka(Y),Ikenoue(S),Ueno(A),Masugi(Y),Yam... Eur J Med Genet 2025-10-00

...RIT1-associated mirror syndrome and non-immune hydrops fetalis (NIHF) further supports the role of Rasopathies in the pa...

Clinical and molecular analysis of seventy-one fetal cases with RASopathies.

Yu(QX),Zhen(L),Zhang(YL),Li(SY),Li(R),Li(D... Eur J Obstet Gynecol Reprod... 2025-11-00

...RIT1, SHOC2, and SOS1. The most significant contributor among these variants was PTPN11 (43.7 %; 31/71), followed by RAF...

Structural basis for LZTR1 recognition of RAS GTPases for degradation.

Dharmaiah(S),Bonsor(DA),Mo(SP),Fernandez-C... Science 2025-09-11

...RIT1, MRAS, and KRAS, revealing interfaces that govern RAS isoform selectivity and nucleotide specificity. Biochemical a...

Mutant RIT1 cooperates with YAP to drive an EMT-like lung cancer state.

Rominger(MC),O'Brien(S),Gupta(S),Moorthi(S... Cell Rep 2025-10-28

...RIT1 may act as a non-canonical driver oncogene in lung cancer. However, the lack of a RIT1-mutant lung cancer model has...

Spectrum of mutations and genotype-phenotype analysis in Noonan syndrome pati...

Yaoita(Masako),Niihori(Tetsuya),Mizuno(Sei... Hum Genet 2016-05-20

...RIT1 mutation-positive patients, we further performed a RIT1 analysis in RASopathy patients and identified 7 RIT1 mutati...

Elevated expression of RIT1 correlates with poor prognosis in endometrial can...

Xu(Fengjuan),Sun(Su'an),Yan(Shilan),Guo(Ho... Int J Clin Exp Pathol 2016-10-05

...RIT1 and assess the clinical significance of RIT1 expression in endometrial cancer patients. The mRNA and protein expres...

New Mutations Associated with Rasopathies in a Central European Population an...

Čizmárová(M),Hlinková(K),Bertok(S),Kotnik(... Ann Hum Genet 2016-05-31

...RIT1, one in SHOC2, two in HRAS, three in BRAF, two in MAP2K1 and two in the NF1 gene). Two of them (p.Gly392Glu in the ...

Profiling of Oncogenic Driver Events in Lung Adenocarcinoma Revealed MET Muta...

Yeung(Sai F),Tong(Joanna H M),Law(Peggy P ... J Thorac Oncol 2016-06-13

...RIT1 mutations by polymerase chain reaction-direct sequencing. MET amplification and ALK and ROS1 translocations were as...

Further evidence of the importance of RIT1 in Noonan syndrome.

Bertola(Débora R),Yamamoto(Guilherme L),Al... Am J Med Genet A 2016-05-16

...RIT1 missense mutations. Thus, we confirm that RIT1 is responsible for approximately 10% of the patients negative for mu...

Comprehensive massive parallel DNA sequencing strategy for the genetic diagno...

Justino(Ana),Dias(Patrícia),João Pina(Mari... Eur J Hum Genet 2015-10-22

...RIT1 were also associated with these syndromes. Because of the genetic and clinical heterogeneity of NCFCS, it is challe...

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