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Chemical profiling, proximate composition, and antibacterial, antioxidant, an...

Sureshkumar(J),Prabhu(S),Mariraj(M),Amalra... Microb Pathog 2026-05-00

...Rit1 had docking scores ranging from -11.496 to -0.012 kcal/mol, whereas those for the T-cell receptor beta chain ranged...

Epithelial Cell-Specific Prognostic Signature (FTH1, RIT1, WASL, NDRG2, KIFC3...

Wang(X),Pan(X),Li(X),Ding(B),Jin(Z),Wang(X... Hum Mutat None

...RIT1, WASL, NDRG2, and KIFC3) was constructed. The resulting risk model effectively stratified patients into high- and l...

Clinical and Molecular Characterization of a RASopathy Cohort From Türkiye an...

Akbaş(ENK),Toksoy(G),Avcı(Ş),Altunoğlu(U),... Clin Genet 2026-07-19

...RIT1, SHOC2, and SOS1. Notably, one patient harbored a variant in AMMECR1, which is not involved in the RAS/MAPK pathway...

Neonatal Noonan syndrome with acute kidney injury and systemic capillary leak...

Gao(C),Kong(F),Tao(X) Front Pediatr None

...RIT1 c.247A>C (p.Thr83Pro), and to expand the understanding of life-threatening presentations in neonatal RIT1 associate...

New Biochemical Insights into RIT GTPases Regulation and Membrane Interaction...

Mirzaiebadizi(A),Bazgir(F),Mosaddeghzadeh(... Cells 2026-08-28

...RIT1 and RIT2 are members of the RAS superfamily of small GTPases, which regulate various cellular processes. RIT1 is wi...

Clinical and Molecular Portraits of Pediatric RASopathies: A Study of 118 Gen...

Genç(A),Sarıkaya(E),Ceylan(AC),Çavdarlı(B)... Clin Genet 2026-09-00

...RIT1, RAF1, HRAS, BRAF, RASA2, KRAS, CBL, SHOC2, and MAP2K2. In addition to well-established genotype-phenotype correlat...

Application of next-generation sequencing in nonimmune hydrops fetalis and it...

Qin(Y),Li(W),Zhu(S),Zhang(S),Fang(R),Kang(... BMC Pregnancy Childbirth 2026-06-10

...RIT1, RAF1, and BRAF) and skeletal disorders (FGFR2, COL1A1, and HSPG2) were the most frequently identified monogenic co...

An Unexpected Result in a Case of Gonadal Dysgenesis: Noonan Syndrome Caused ...

Demirtaş(Ş),Özsu(E),Şıklar(Z),Aycan(Z),Kız... J Clin Res Pediatr Endocrin... 2026-06-16

...RIT1 gene. Noonan syndrome may cause gonadal dysfunction leading to delayed puberty and infertility; however, gonadal dy...

Clinical and Molecular characteristics of kidney and urinary tract congenital...

Ammar(THA),Ahmed(HM),Mohammed(EEA),El-Hari... Mol Biol Rep 2026-05-14

...RIT1 mutation in Egypt and the first confirmed association of RIT1 with renal anomalies in NS-8. Expanding genomic scree...

Detection rate and mutational landscape in extracranial arteriovenous malform...

Schmidt(VF),Schanze(D),Brill(R),Loeser(JH)... BMC Med 2026-04-16

...RIT1, RAF1, and GNA14 (each 0.9%, 1/114). Within the RAS/MAPK pathway, RAS variants (KRAS, HRAS) were linked to more sev...

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