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Expression profiling identifies responder and non-responder phenotypes to interferon-{beta} in multiple sclerosis
S Sturzebecher et al.
Brain 126 (6), (01 Jun 2003)
 
Gene expression profiling of human prostate cancer stem cells reveals a pro-inflammatory phenotype and the importance of extracellular matrix interactions
Richard Birnie et al.
Genome Biology 9 (5), R83 (20 May 2008)
 
Trait correlated expression combined with expression QTL analysis reveals biological pathways and candidate genes affecting water holding capacity of muscle.
Siriluck Ponsuksili et al.
BMC genomics 9, 367 (2008)
Posted by AshwinMistry to expression on Fri Sep 26 2008 at 10:24 UTC | info | related
 
t(3;12)(q26;q14) in polycythemia vera is associated with upregulation of the HMGA2 gene.
C T Storlazzi et al.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 20 (12), 2190-2 (Dec 2006)
Posted by pdagenetica (who is an author) to Rearrangement expression cancer on Thu Sep 25 2008 at 09:17 UTC | info | related
 
Classification of human lung carcinomas by mRNA expression profiling reveals distinct adenocarcinoma subclasses.
A Bhattacharjee et al.
Proceedings of the National Academy of Sciences of the United States of America. 98 (24), 13790-5 (20 Nov 2001)
 
Gene module level analysis: identification to networks and dynamics
Current Opinion in Biotechnology, (2008)
Recent, to read
 
p53 regulates TLR3 expression and function in human epithelial cell lines.
Manabu Taura et al.
Molecular and cellular biology, (08 Sep 2008)
Posted by saumen to TLR3 expression p53 on Thu Sep 18 2008 at 15:28 UTC | info | related
 
Biomechanical Modeling of Soft Tissue and Facial Expressions for Craniofacial Surgery Planning
www.diss.fu-berlin.de
The present thesis deals with the numerical modeling of facial tissue biomechanics for the prediction of the patient's postoperative appearance in cranio-, dento-maxillofacial surgery planning. Typically, craniofacial surgery interventions consist in the rearrangement of facial bones, which induces the deformation of surrounding soft tissue. The postoperative patient's appearance has to be predicted on the basis of 3D geometrical models derived from tomographic data and the prescribed displacements of relocated bone structures. The linear elastic approach known from the previous works and widely used in soft tissue modeling is generally limited by the assumption of small deformations and implies a substantial error by ad hoc calculations of large deformations. The investigations carried out in this work lead to the development of a more accurate and flexible non-linear elastic approach. Different tissue types are modeled as a homogeneous, isotropic, quasi-incompressible St. Venant-Kirchhoff material characterized by two elastic constants, the Young modulus describing the material stiffness and the Poisson ratio describing the material compressibility. The numerical solution of the associated discrete boundary value problem on tetrahedral grids is obtained via the finite element method (FEM). Since the non-linear elastic FEM is in general very expensive, an adaptive numerical scheme for the efficient and robust computation of both small and large deformations with user-defined precision is developed. The modelling approach has been validated by the direct comparison between the simulation outcome and the patient's postoperative facial outline in a number of clinical studies. In addition to the static soft tissue prediction, we present a new approach for the estimation of individual facial emotion expressions. We assume natural physiological mechanism of facial expressions that is the impact of contracting muscles on remaining facial tissue. Using this technique, single muscle actions as well as complex individual facial emotion expressions can be estimated.
 
Why highly expressed proteins evolve slowly
Proceedings of the National Academy of Sciences of the United States of America. 102 (40), 14338-43 (04 Oct 2005)
 
Analysis of gene expression in operons of Streptomyces coelicolor
Emma Laing et al.
Genome Biology 7 (6), R46 (02 Jun 2006)

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