...FBN1 deletion. This was confirmed on proband's chromosome microarray; however, the mother was negative for the FBN1 dele...
...FBN1 (GD2) or LTBP3 (GD3). GD is characterized by severe short stature and other skeletal abnormalities, characteristic ...
...FBN1 and TGF-beta signaling), increasingly linked to diagnosis, variant interpretation, risk stratification, guidelines,...
...Fbn1+/+ and Fbn1C1041G/+ littermates were infused with either AngII or norepinephrine via subcutaneously implanted osmot...
...FBN1 gene (c.3333C > A and c.8854_8562delinsTATCAC). Both lines exhibited typical iPSC morphology, normal karyotype, und...
...FBN1 involved in ECM remodeling and cell adhesion. SASP promotes ovarian cancer cell adhesion through MMP-mediated ECM d...
...Fbn1 locus, generating a durable transcriptional state associated with sustained Fbn1 expression and plasma asprosin ele...
...Fbn1) showing the greatest increase (632-fold). Structural ECM components, in particular glycoproteins, constituted the ...
...FBN1 (fibrillin-1) protein regulation in both human and mouse Marfan syndrome, and position single-cell proteomics as a ...
...FBN1, Rac1-GTP, Myosin IIB, cytoskeletal scaffolding proteins, and crystallin aggregation. Diabetic conditions induced a...
山东省济南市章丘区文博路2号
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