Results 51 to 60 of about 9,658 (265)
Fluorescent probes allow dynamic visualization of phosphoinositides in living cells (left), whereas mass spectrometry provides high‐sensitivity, isomer‐resolved quantitation (right). Their synergistic use captures complementary aspects of lipid signaling. This review illustrates how these approaches reveal the spatiotemporal regulation and quantitative
Hiroaki Kajiho +3 more
wiley +1 more source
The characterization of inverses of symmetric tridiagonal and block tridiagonal matrices and the development of algorithms for finding the inverse of any general non-singular tridiagonal matrix are subjects that have been studied by many authors.
C. G. Almeida, S. A. E. Remigio
doaj +1 more source
Integrative factorization of bidimensionally linked matrices [PDF]
AbstractAdvances in molecular “omics” technologies have motivated new methodologies for the integration of multiple sources of high‐content biomedical data. However, most statistical methods for integrating multiple data matrices only consider data shared vertically (one cohort on multiple platforms) or horizontally (different cohorts on a single ...
Jun Young Park, Eric F. Lock
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Embryo‐like structures (stembryos) are an innovative tool, but they are hindered by experimental variability and limited developmental potential. DNA methylation is crucial for mammalian development, but its status in stembryo models is poorly characterized.
Sara Canil +4 more
wiley +1 more source
On Symmetric Factorizations of Hankel Matrices
We present two conjectures regarding the running time of computing symmetric factorizations for a Hankel matrix $\mathbf{H}$ and its inverse $\mathbf{H}^{-1}$ as $\mathbf{B}\mathbf{B}^*$ under fixed-point arithmetic. If solved, these would result in a faster-than-matrix-multiplication algorithm for solving sparse poly-conditioned linear programming ...
openaire +2 more sources
Block LU factorizations of M-matrices [PDF]
It is well known that any nonsingular M-matrix admits an LU factorization into M-matrices (with L and U lower and upper triangular respectively) and any singular M-matrix is permutation similar to an M-matrix which admits an LU factorization into M-matrices.
Judith J. McDonald, Hans Schneider
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Septin 9 polybasic domains couple phosphoinositide‐rich membrane binding to centrosome positioning, Golgi organization, and microtubule acetylation to control epithelial polarity. Their loss disrupts this axis, causing centrosome mispositioning, Golgi fragmentation, reduced microtubule acetylation, and polarity inversion via upregulation of the ...
Ting ting Cai +4 more
wiley +1 more source
This study reveals that the small GTPase Rab14 is necessary for human papillomavirus (HPV) infection and plays an essential role in the transport of virions to the trans‐Golgi network (TGN). HPV in the early endosome (EE), which harbors GTP‐bound Rab14, is transported to the TGN through the switch of Rab14 from its GTP‐bound to GDP‐bound form.
Yoshiyuki Ishii, Iwao Kukimoto
wiley +1 more source
Characterizing Variability of Modular Brain Connectivity with Constrained Principal Component Analysis. [PDF]
Characterizing the variability of resting-state functional brain connectivity across subjects and/or over time has recently attracted much attention.
Jun-Ichiro Hirayama +4 more
doaj +1 more source
On theLU factorization ofM-matrices
In this paper, we give in Theorem 1 a characterization, based on graph theory, of when anM-matrixA admits anLU factorization intoM-matrices, whereL is a nonsingular lower triangularM-matrix andU is an upper triangularM-matrix. This result generalizes earlier factorization results of Fiedler and Ptak (1962) and Kuo (1977). As a consequence of Theorem 1,
VARGA, R.S., Cai, D.Y.
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