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[A rare case of myeloproliferative disease with t(8;13)(p11;q12) associated w...

Tsyba(N N),Turkina(A G),Chelysheva(E Yu),N... Ter Arkh 0000-00-00

...PDGFRB (5q32-33). The similar changes in the karyotype were also found in the lymph node cells. The undertaken treatment...

Methylation analysis of plasma cell-free DNA for breast cancer early detectio...

Li(Zibo),Guo(Xinwu),Tang(Lili),Peng(Limin)... Tumour Biol 0000-00-00

...PDGFRB, PPM1E, SOX17, and WRN) in plasma cfDNA as biomarkers for breast cancer early detection, quantitative analysis of...

Placental structural abnormalities have detrimental hemodynamic consequences ...

Lehtoranta(Lara),Vuolteenaho(Olli),Laine(J... Placenta 0000-00-00

...Pdgfrb), and tumor necrosis factor receptor superfamily, member 12α (Tnfrsf12α) expressions were decreased. Interleukin ...

Cytochrome P450 1B1 Contributes to the Development of Angiotensin II-Induced ...

Thirunavukkarasu(Shyamala),Khan(Nayaab S),... Am J Pathol 0000-00-00

...Pdgfrb, Itga2, and matrix metalloproteinases 2 and 9 expression in aortic lesions; these changes were inhibited in mice ...

Sunitinib-induced morpho-functional changes and drug effectiveness in maligna...

Spagnuolo(Rosalin D),Brich(Silvia),Bozzi(F... Oncotarget 0000-00-00

...PDGFRB expression and decreased mTOR signalling, and corresponded to a pathological response. The second were associated...

XPR1 mutations are a rare cause of primary familial brain calcification.

Anheim(Mathieu),López-Sánchez(Uriel),Giova... J Neurol 0000-00-00

...PDGFRB mutation. XPR1 variants were tested in an in vitro physiological complementation assay and patient blood cells we...

Identification of partial SLC20A2 deletions in primary brain calcification us...

David(Stéphanie),Ferreira(Joana),Quenez(Ol... Eur J Hum Genet 0000-00-00

...PDGFRB and XPR1. We used the CANOES tool to detect copy number variations (CNVs). We detected two deletions of exon 2 of...

Early-Stage Loeffler's Endocarditis with Isolated Right Ventricular Involveme...

Beedupalli(Jagan),Modi(Kalgi) Echocardiography 0000-00-00

...PDGFRB mutation, abnormal myeloid maturation, or a lymphoproliferative disorder. Flow cytometry showed no clonality excl...

Moyamoya vasculopathy shows a genetic mutational gradient decreasing from Eas...

Raso(Alessandro),Biassoni(Roberto),Mascell... J Neurosurg Sci 0000-00-00

...PDGFRB in 21 ethnically homogeneous Italian children with moyamoya; comprehensive sequencing data are available from par...

Recurrent Somatic PDGFRB Mutations in Sporadic Infantile/Solitary Adult Myofi...

Agaimy(Abbas),Bieg(Matthias),Michal(Michae... Am J Surg Pathol 0000-00-00

...PDGFRB mutations. We detected PDGFRB mutations in 6/8 (75%) analyzable infantile and in 11/16 (69%) adult MFs but in non...

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