Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Karin Roesch"'
Publikováno v:
Clinical Ophthalmology (Auckland, N.Z.)
Karin Roesch, Tristan Swedish, Ramesh Raskar MIT Media Lab, Massachusetts Institute of Technology, Cambridge, MA, USA Abstract: Most current diagnostic devices are expensive, require trained specialists to operate and gather static images with sparse
Autor:
Jia Yin, Zala Lužnik, Gerrit R. J. Melles, Reza Dana, Karin Roesch, Lars Franken, Silke Oellerich, Markus Zumbansen
Publikováno v:
Ophthalmology
A retrospective case-control study found significantly increased levels of interleukin-5 and interleukin-8, critical cytokines of the innate immune system, in the aqueous humor of patients undergoing repeat DMEK for graft failure, compared to primary
Publikováno v:
EMBC
MIT web domain
MIT web domain
Medical data presents a number of challenges. It tends to be unstructured, noisy and protected. To train algorithms to understand medical images, doctors can label the condition associated with a particular image, but obtaining enough labels can be d
Autor:
Jeffrey M. Trimarchi, Ben B. Sun, Michael B. Stadler, Ashutosh P Jadhav, Botond Roska, Karin Roesch, Connie Cepko
Publikováno v:
The Journal of Comparative Neurology
Müller glial cells are the major type of glia in the mammalian retina. To identify the molecular machinery that defines Müller glial cell identity and function, single cell gene expression profiling was performed on Affymetrix microarrays. Identifi
Human deafness dystonia syndrome is caused by a defect in assembly of the DDP1/TIMM8a-TIMM13 complex
Publikováno v:
Human Molecular Genetics. 11:477-486
Mohr-Tranebjaerg syndrome (MTS/DFN-1) or deafness/dystonia syndrome results from a mutation in deafness/ dystonia protein 1/translocase of mitochondrial inner membrane 8a (DDP1/TIMM8a). DDP1/TIMM8a is similar to a family of yeast proteins in the mito
Autor:
Hana Hansikova, Carla M. Koehler, Jan Hadač, Anna Sediva, Jiří Zeman, Hans D. Ochs, Takeshi Futatani, Lenka Mrázová, Karin Roesch, Lenka Dvořáková, C. I. Edvard Smith, Sirje Velbri, Ales Janda, A. Charlotta Asplund, Kathleen E. Sullivan
Publikováno v:
Journal of clinical immunology. 27(6)
X-linked agammaglobulinemia (XLA) is characterized by low levels of B-lymphocytes with early-onset, recurrent, microbial infections occasionally causing neurological symptoms. We observed an atypical clinical course of XLA, complicated since early ch
Publikováno v:
Human molecular genetics. 13(18)
The biogenesis of the mitochondrial inner membrane is dependent on two distinct 70 kDa protein complexes. TlMM8a partners with TIMM13 in the mitochondrial intermembrane space to form a 70 kDa complex and facilitates the import of the inner membrane s