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Actin filaments Aggresome Cell Junctions Centrosome Cleavage furrow Cytokinetic bridge Cytoplasmic bodies Cytosol Endoplasmic reticulum Endosomes Focal adhesion sites Golgi apparatus Intermediate filaments Lipid droplets Lysosomes Microtubule ends Microtubule organizing center Microtubules Midbody Midbody ring Mitochondria Mitotic spindle Nuclear bodies Nuclear membrane Nuclear speckles Nucleoli Nucleoli fibrillar center Nucleoplasm Nucleus Peroxisomes Plasma membrane Rods & Rings Vesicles Searches. Any A-431 A549 AF22 AN3-CA ASC diff ASC TERT1 BEWO BJ BJ hTERT+ BJ hTERT+ SV40 Large T+ BJ hTERT+ SV40 Large T+ RasG12V CACO-2 CAPAN-2 Daudi EFO-21 FHDF/TERT166 HaCaT HAP1 HBEC3-KT HBF TERT88 HDLM-2 HEK 293 HEL HeLa Hep G2 HHSteC HL-60 HMC-1 HSkMC HTCEpi HTEC/SVTERT24-B HTERT-HME1 HUVEC TERT2 K-562 Karpas-707 LHCN-M2 MCF7 MOLT-4 NB-4 NTERA-2 PC-3 REH RH-30 RPMI-8226 RPTEC TERT1 RT4 SCLC-21H SH-SY5Y SiHa SK-BR-3 SK-MEL-30 T-47d THP-1 TIME U-138 MG U-2 OS U-2197 U-251 MG U-266/70 U-266/84 U-698 U-87 MG U-937 WM-115 Specificity. Any A-431 A549 AF22 AN3-CA ASC diff ASC TERT1 BEWO BJ BJ hTERT+ BJ hTERT+ SV40 Large T+ BJ hTERT+ SV40 Large T+ RasG12V CACO-2 CAPAN-2 Daudi EFO-21 FHDF/TERT166 HaCaT HAP1 HBEC3-KT HBF TERT88 HDLM-2 HEK 293 HEL HeLa Hep G2 HHSteC HL-60 HMC-1 HSkMC HTCEpi HTEC/SVTERT24-B HTERT-HME1 HUVEC TERT2 K-562 Karpas-707 LHCN-M2 MCF7 MOLT-4 NB-4 NTERA-2 PC-3 REH RH-30 RPMI-8226 RPTEC TERT1 RT4 SCLC-21H SH-SY5Y SiHa SK-BR-3 SK-MEL-30 T-47d THP-1 TIME U-138 MG U-2 OS U-2197 U-251 MG U-266/70 U-266/84 U-698 U-87 MG U-937 WM-115 Detectable.
Jan 23, 2019 - Links will be added as guides are published. Publication Date: 2017. Miller's review of Orthopaedics by Mark D. Miller; Stephen R. Thompson; Jennifer Hart. Weir and Abrahams' imaging atlas of human anatomy by Jonathan D. Imhoff (Editor); Knut Beitzel (Editor); Knut Stamer (Editor); Elke Klein.
Understanding the connectivity architecture of entire vertebrate brains is a fundamental but difficult task. Here we present an integrated neuro-histological pipeline as well as a grid-based tracer injection strategy for systematic mesoscale connectivity mapping in the common marmoset ( Callithrix jacchus). Individual brains are sectioned into ~1700 20 µm sections using the tape transfer technique, permitting high quality 3D reconstruction of a series of histochemical stains (Nissl, myelin) interleaved with tracer labeled sections. Systematic in-vivo MRI of the individual animals facilitates injection placement into reference-atlas defined anatomical compartments. Further, by combining the resulting 3D volumes, containing informative cytoarchitectonic markers, with in-vivo and ex-vivo MRI, and using an integrated computational pipeline, we are able to accurately map individual brains into a common reference atlas despite the significant individual variation.
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This approach will facilitate the systematic assembly of a mesoscale connectivity matrix together with unprecedented 3D reconstructions of brain-wide projection patterns in a primate brain. The connectional architecture of the brain underlies all the nervous system functions, yet our knowledge of detailed brain neural connectivity falls largely behind genomics and behavioral studies in humans and in model research species such as rodents (). To fill this critical gap, a coherent approach for the mapping of whole-brain neural circuits at the mesoscale using standardized methodology was proposed in 2009 (). Since then, several systematic brain connectivity mapping projects for the mouse have been initialized and established, including the Mouse Brain Architecture Project () (), the Allen Mouse Brain Connectivity Atlas () (connectivity.brain-map.org), and the Mouse Connectome Project ( (). Non-human primates (NHPs) were also proposed as an important group in which to study whole-brain neural architecture. However, the high-throughput experimental approaches for mouse do not automatically apply to NHPs due to bioethical as well as experimental considerations, larger brain sizes coupled with stringent limitations on the numbers, as well as limitations arising from the increased individual variability of the brains. There has been an increase in the usage of the common marmoset ( Callithrix jacchus) as a model organism in contemporary neuroscience research (;;;; ) ().
Marmosets offer a number of experimental advantages over the macaque, including lower cost, ease of handling and breeding (; ), smaller brain sizes (≈35 mm*25 mm*20 mm) that potentially allow more comprehensive analysis of the neuronal circuitry, and importantly the development of transgenic marmosets and the application of modern molecular tools (;; ). Marmosets are New World monkeys, in contrast with the Old World macaque monkeys which are the pre-eminent NHP models used in basic and pre-clinical neuroscience research. As depicted in, New World monkeys, together with Old World monkeys, apes and humans, form the simian primates (order Primates, infraorder Simiiformes). Simians diverged from prosimians such as lemurs and lorises approximately 85 million years ago (Mya). Among the simians, New World monkeys have evolved in isolation from Old World monkeys, apes and humans for at least 40 million years.
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AnyMusic allows you to download all videos from a YouTube playlist at a time. By the way, you can also convert these music videos to audio formats within 1 application! Justin Timberlake Tour 2018 Here I listed Justin’s tour plan in upcoming March. You just need to copy and paste the YouTube playlist link () to the search bar of AnyMusic, and click “All” then you can enjoy offline listening.
Actin filaments Aggresome Cell Junctions Centrosome Cleavage furrow Cytokinetic bridge Cytoplasmic bodies Cytosol Endoplasmic reticulum Endosomes Focal adhesion sites Golgi apparatus Intermediate filaments Lipid droplets Lysosomes Microtubule ends Microtubule organizing center Microtubules Midbody Midbody ring Mitochondria Mitotic spindle Nuclear bodies Nuclear membrane Nuclear speckles Nucleoli Nucleoli fibrillar center Nucleoplasm Nucleus Peroxisomes Plasma membrane Rods & Rings Vesicles Searches. Any A-431 A549 AF22 AN3-CA ASC diff ASC TERT1 BEWO BJ BJ hTERT+ BJ hTERT+ SV40 Large T+ BJ hTERT+ SV40 Large T+ RasG12V CACO-2 CAPAN-2 Daudi EFO-21 FHDF/TERT166 HaCaT HAP1 HBEC3-KT HBF TERT88 HDLM-2 HEK 293 HEL HeLa Hep G2 HHSteC HL-60 HMC-1 HSkMC HTCEpi HTEC/SVTERT24-B HTERT-HME1 HUVEC TERT2 K-562 Karpas-707 LHCN-M2 MCF7 MOLT-4 NB-4 NTERA-2 PC-3 REH RH-30 RPMI-8226 RPTEC TERT1 RT4 SCLC-21H SH-SY5Y SiHa SK-BR-3 SK-MEL-30 T-47d THP-1 TIME U-138 MG U-2 OS U-2197 U-251 MG U-266/70 U-266/84 U-698 U-87 MG U-937 WM-115 Specificity. Any A-431 A549 AF22 AN3-CA ASC diff ASC TERT1 BEWO BJ BJ hTERT+ BJ hTERT+ SV40 Large T+ BJ hTERT+ SV40 Large T+ RasG12V CACO-2 CAPAN-2 Daudi EFO-21 FHDF/TERT166 HaCaT HAP1 HBEC3-KT HBF TERT88 HDLM-2 HEK 293 HEL HeLa Hep G2 HHSteC HL-60 HMC-1 HSkMC HTCEpi HTEC/SVTERT24-B HTERT-HME1 HUVEC TERT2 K-562 Karpas-707 LHCN-M2 MCF7 MOLT-4 NB-4 NTERA-2 PC-3 REH RH-30 RPMI-8226 RPTEC TERT1 RT4 SCLC-21H SH-SY5Y SiHa SK-BR-3 SK-MEL-30 T-47d THP-1 TIME U-138 MG U-2 OS U-2197 U-251 MG U-266/70 U-266/84 U-698 U-87 MG U-937 WM-115 Detectable.
Jan 23, 2019 - Links will be added as guides are published. Publication Date: 2017. Miller's review of Orthopaedics by Mark D. Miller; Stephen R. Thompson; Jennifer Hart. Weir and Abrahams' imaging atlas of human anatomy by Jonathan D. Imhoff (Editor); Knut Beitzel (Editor); Knut Stamer (Editor); Elke Klein.
Understanding the connectivity architecture of entire vertebrate brains is a fundamental but difficult task. Here we present an integrated neuro-histological pipeline as well as a grid-based tracer injection strategy for systematic mesoscale connectivity mapping in the common marmoset ( Callithrix jacchus). Individual brains are sectioned into ~1700 20 µm sections using the tape transfer technique, permitting high quality 3D reconstruction of a series of histochemical stains (Nissl, myelin) interleaved with tracer labeled sections. Systematic in-vivo MRI of the individual animals facilitates injection placement into reference-atlas defined anatomical compartments. Further, by combining the resulting 3D volumes, containing informative cytoarchitectonic markers, with in-vivo and ex-vivo MRI, and using an integrated computational pipeline, we are able to accurately map individual brains into a common reference atlas despite the significant individual variation.
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This approach will facilitate the systematic assembly of a mesoscale connectivity matrix together with unprecedented 3D reconstructions of brain-wide projection patterns in a primate brain. The connectional architecture of the brain underlies all the nervous system functions, yet our knowledge of detailed brain neural connectivity falls largely behind genomics and behavioral studies in humans and in model research species such as rodents (). To fill this critical gap, a coherent approach for the mapping of whole-brain neural circuits at the mesoscale using standardized methodology was proposed in 2009 (). Since then, several systematic brain connectivity mapping projects for the mouse have been initialized and established, including the Mouse Brain Architecture Project () (), the Allen Mouse Brain Connectivity Atlas () (connectivity.brain-map.org), and the Mouse Connectome Project ( (). Non-human primates (NHPs) were also proposed as an important group in which to study whole-brain neural architecture. However, the high-throughput experimental approaches for mouse do not automatically apply to NHPs due to bioethical as well as experimental considerations, larger brain sizes coupled with stringent limitations on the numbers, as well as limitations arising from the increased individual variability of the brains. There has been an increase in the usage of the common marmoset ( Callithrix jacchus) as a model organism in contemporary neuroscience research (;;;; ) ().
Marmosets offer a number of experimental advantages over the macaque, including lower cost, ease of handling and breeding (; ), smaller brain sizes (≈35 mm*25 mm*20 mm) that potentially allow more comprehensive analysis of the neuronal circuitry, and importantly the development of transgenic marmosets and the application of modern molecular tools (;; ). Marmosets are New World monkeys, in contrast with the Old World macaque monkeys which are the pre-eminent NHP models used in basic and pre-clinical neuroscience research. As depicted in, New World monkeys, together with Old World monkeys, apes and humans, form the simian primates (order Primates, infraorder Simiiformes). Simians diverged from prosimians such as lemurs and lorises approximately 85 million years ago (Mya). Among the simians, New World monkeys have evolved in isolation from Old World monkeys, apes and humans for at least 40 million years.