Results 71 to 80 of about 19,221,852 (336)

Violation of Bell's Inequality with Photons from Independent Sources [PDF]

, 2003
We report a violation of Bell's inequality using one photon from a parametric down-conversion source and a second photon from an attenuated laser beam. The two photons were entangled at a beam splitter using the post-selection technique of Shih and Alley
A. Aspect, A. I. Lvovsky, A. I. Lvovsky, G. Di Giuseppe, J. D. Franson, J. G. Rarity, J. S. Bell, K. J. Resch, K. J. Resch, M. Zukowski, R. P. Feynman, T. B. Pittman, W. P. Grice, Z. Y. Ou   +13 more
core   +2 more sources

KLK7 overexpression promotes an aggressive phenotype and facilitates peritoneal dissemination in colorectal cancer cells

FEBS Open Bio, EarlyView.
KLK7, a tissue kallikrein‐related peptidase, is elevated in advanced colorectal cancer and associated with shorter survival. High KLK7 levels in ascites correlate with peritoneal metastasis. In mice, KLK7 overexpression increases metastasis. In vitro, KLK7 enhances cancer cell proliferation, migration, adhesion, and spheroid formation, driving ...
Yosr Z. Haffani, Tobias Dreyer, Meriem Naim, Rea Lo Dico, Natalia A. Ignatenko, Viktor Magdolen, Dalila Darmoul   +6 more
wiley   +1 more source

Finite-Field Ground State of the S=1 Antiferromagnetic-Ferromagnetic Bond-Alternating Chain

, 2004
We investigate the finite-field ground state of the S=1 antiferromagnetic-ferromagnetic bond-alternating chain described by the Hamiltonian ${\calH}=\sum\nolimits_{\ell}\bigl\{\vecS_{2\ell-1}\cdot\vecS_{2\ell} +J\vecS_{2\ell}\cdot\vecS_{2\ell+1}\bigr ...
Berezinskii Z. L., Bonner J. C., Chen W., Kitazawa A., Kitazawa A., Nomura K., Tonegawa T., Tonegawa T., White S. R.   +8 more
core   +1 more source

Domain associated with zinc fingers‐containing NF90‐NF45 complex inhibits m6A modification of primary microRNA by suppressing METTL3/14 activity

FEBS Open Bio, EarlyView.
NF90–NF45 functions as a negative regulator of methyltransferase‐like 3/14 (METTL3/14)‐mediated N6‐methyladenosine (m6A) modification on primary microRNAs (pri‐miRNAs). NF90–NF45 binds to anti‐oncogenic pri‐miRNAs and inhibits their m6A modification, thereby suppressing the biogenesis of anti‐oncogenic miRNAs.
Takuma Higuchi, Shunsuke Morioka, Keiko Morisawa, Kazutsugu Matsukawa, Shingo Ashida, Takeshi Suzuki, Shuji Sakamoto   +6 more
wiley   +1 more source

Characterization of glucose metabolism in youth with vs. without cystic fibrosis liver disease: A pilot study

Journal of Clinical & Translational Endocrinology, 2022
Background: Diabetes and liver disease are life-threatening complications of cystic fibrosis (CF). CF-liver disease is a risk factor for CF related diabetes (CFRD) development, but the underlying mechanisms linking the two co-morbidities are not known ...
Maria Socorro Rayas, Kara S. Hughan, Rida Javaid, Andrea Kelly, Marzieh Salehi   +4 more
doaj   +1 more source

Online yoga to reduce post traumatic stress in women who have experienced stillbirth: a randomized control feasibility trial

BMC Complementary Medicine and Therapies, 2020
Background About 1 in every 150 pregnancies end in stillbirth. Consequences include symptoms of post traumatic stress disorder (PTSD), depression, and anxiety.
J. Huberty, Maria Sullivan, Jeni Green, J. Kurka, J. Leiferman, K. Gold, Joanne Cacciatore   +6 more
semanticscholar   +1 more source

Probabilistic Quantum Encoder for Single-Photon Qubits

, 2003
We describe an experiment in which a physical qubit represented by the polarization state of a single-photon was probabilistically encoded in the logical state of two photons.
A. V. Belinsky, B. C Jacobs, D. M. Greenberger, J. D. Franson, J. G. Rarity, M. A. Nielsen, M. Zukowski, T. B. Pittman, T. B. Pittman   +8 more
core   +1 more source

Growth Differentiation Factor 15 Elevation in the Central Nervous System Is Associated With Failure to Thrive in Alexander Disease

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Alexander disease (AxD) is a severe neurodegenerative disorder caused by gain‐of‐function mutations in the gene for GFAP, which lead to protein aggregation and a primary astrocytopathy. Symptoms vary, but failure to thrive (FTT) and frequent emesis are common and cause significant morbidity. Here we investigate GDF15, a member of the
Tracy L. Hagemann, Michelle M. Sonsalla, Cora Luzinski, Fernando Zacahua, David A. Harris, Dudley W. Lamming, Albee Messing   +6 more
wiley   +1 more source

Experimental realization of optimal asymmetric cloning and telecloning via partial teleportation

, 2005
We report an experimental realization of both optimal asymmetric cloning and telecloning of single photons by making use of partial teleportation of an unknown state.
An-Ning Zhang, Anders Karlsson, Chao-Yang Lu, Jian-Wei Pan, M. Zukowski, Xiao-Qi Zhou, Yu-Ao Chen, Zhi Zhao   +7 more
core   +1 more source

SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SNUPN‐related muscular dystrophy or LGMDR29 is a new entity that covers from a congenital or childhood onset pure muscular dystrophy to more complex phenotypes combining neurodevelopmental features, cataracts, or spinocerebellar ataxia. So far, 12 different variants have been described.
Nuria Muelas, Pablo Iruzubieta, Alberto Damborenea, Laura Pérez‐Fernández, Inmaculada Azorín, Juan Carlos Jiménez García, Ana Töpf, Pilar Martí, Lorena Fores‐Toribio, María Manterola, Rosana Blanco‐Mañez, Oihane Pikatza‐Menoio, Sonia Alonso‐Martín, Volker Straub, Aitziber L. Cortajarena, Adolfo López de Munain, David De Sancho, Lorea Blázquez, Juan J. Vilchez   +18 more
wiley   +1 more source