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Extreme X-Ray Reflection in the Nucleus of the Seyfert Galaxy NGC 5033
Abstract
NGC 5033 is an intriguing Seyfert galaxy because its subclassification may change with time, and because optical and submillimeter observations find that the massive black...
SB Yun, JM Miller, D Barret, D Stern, WN Brandt, L Brenneman, P Draghis, AC Fabian, J Raymond, A Zoghbi
Aug 10, 2022
Exotic bilayer crystals in a strong magnetic field
Electron bilayers in a strong magnetic field exhibit insulating behavior for a wide range of interlayer separation d for total Landau level fillings ν ≤ 1 / 2 , which has been interpreted in terms of a pinned crystal. We study...
Polymerization of low molecular weight hydrogelators to form electrochromic polymers
Petra Cameron, Salmah Awhida, Christopher Hotchen, Wentao Deng, Ben Alston, Tom O. McDonald, Dave J. Adams, Peter Kubiak
Jul 04, 2015
We present a method for the polymerization of low molecular weight hydrogelators to form polymers with unique structures. Carbazole-protected amino acids are shown to form hydrogels by self-assembly into fibrous structures. We...
Polymerization of low molecular weight hydrogelators to form electrochromic polymers
Petra Cameron, Salmah Awhida, Christopher Hotchen, Wentao Deng, Ben Alston, Tom O. McDonald, Dave J. Adams, Peter Kubiak
Jul 04, 2015
We present a method for the polymerization of low molecular weight hydrogelators to form polymers with unique structures. Carbazole-protected amino acids are shown to form hydrogels by self-assembly into fibrous structures. We...
Consistent Analysis of the AGN LF in X-Ray and MIR in the XMM-LSS Field
Abstract
The luminosity function of active galactic nuclei (AGN) probes the history of supermassive black hole assembly and growth across cosmic time. To mitigate selection biases...
J Runburg, D Farrah, A Sajina, M Lacy, J Lidua, E Hatziminaoglou, WN Brandt, CTJ Chen, K Nyland, R Shirley, DL Clements, LK Pitchford
Jan 28, 2022
Molecular genetic investigations identify new clinical phenotypes associated with BCS1L-related mitochondrial disease.
Monika Oláhová, Camilla Ceccatelli Berti, Jack J Collier, Charlotte L Alston, Elisabeth Jameson, Simon A Jones, Noel Edwards, Langping He, Patrick F Chinnery, Rita Horvath, Paola Goffrini, Robert W Taylor, John A Sayer
Sep 04, 2019
BCS1L encodes a homolog of the Saccharomyces cerevisiae bcs1 protein, which has a known role in the assembly of Complex III of the mitochondrial respiratory chain. Phenotypes reported in association with pathogenic BCS1L...
ATPases Associated with Diverse Cellular Activities acidosis Lactic Adult Amino Acid Sequence Cholestasis Electron Transport Complex III Female Fetal Growth Retardation FIBROBLASTS Hemosiderosis Humans Infant Male metabolism Inborn Errors Mitochondrial Diseases Muscle Skeletal Mutation Phenotype Renal Aminoacidurias
Adipose tissue dysfunction as a central mechanism leading to dysmetabolic obesity triggered by chronic exposure to p,p'-DDE
D Pestana, D Teixeira, M Meireles, C Marques, S Norberto, C Sá, VC Fernandes, L Correia-Sá, A Faria, L Guardão, JT Guimarães, WN Cooper, I Sandovici, VF Domingues, C Delerue-Matos, R Monteiro, M Constância, C Calhau
Aug 25, 2017
Accurate mitochondrial DNA sequencing using off-target reads provides a single test to identify pathogenic point mutations.
Helen R Griffin, Angela Pyle, Emma L Blakely, Charlotte L Alston, Jennifer Duff, Gavin Hudson, Rita Horvath, Ian J Wilson, Mauro Santibanez-Koref, Robert W Taylor, Patrick F Chinnery
Mar 07, 2019
PURPOSE: Mitochondrial disorders are a common cause of inherited metabolic disease and can be due to mutations affecting mitochondrial DNA or nuclear DNA. The current diagnostic approach involves the targeted resequencing of...
$^{18}$F-Fluoride and $^{18}$F-Fluorodeoxyglucose Positron Emission Tomography After Transient Ischemic Attack or Minor Ischemic Stroke
AT Vesey, WSA Jenkins, A Irkle, A Moss, G Sng, RO Forsythe, T Clark, G Roberts, A Fletcher, C Lucatelli, JHF Rudd, AP Davenport, NL Mills, R Al-Shahi Salman, M Dennis, WN Whiteley, EJR van Beek, MR Dweck, DE Newby
Mar 16, 2017
Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease.
Gráinne S Gorman, Andrew M Schaefer, Yi Ng, Nicholas Gomez, Emma L Blakely, Charlotte L Alston, Catherine Feeney, Rita Horvath, Patrick Yu-Wai-Man, Patrick F Chinnery, Robert W Taylor, Douglass M Turnbull, Robert McFarland
Mar 07, 2019
OBJECTIVE: The prevalence of mitochondrial disease has proven difficult to establish, predominantly as a result of clinical and genetic heterogeneity. The phenotypic spectrum of mitochondrial disease has expanded significantly...
The response of relativistic outflowing gas to the inner accretion disk of a black hole
Michael L Parker, Ciro Pinto, Andrew C Fabian, Anne Lohfink, Douglas JK Buisson, William N Alston, Erin Kara, Edward M Cackett, Chia-Ying Chiang, Thomas Dauser, Barbara De Marco, Luigi C Gallo, Javier Garcia, Fiona A Harrison, Ashley L King, Matthew J Middleton, Jon M Miller, Giovanni Miniutti, Christopher S Reynolds, Phil Uttley, Ranjan Vasudevan, Dominic J Walton, Daniel R Wilkins, Abderahmen Zoghbi
May 03, 2018
The geometry of the infrared and x-ray obscurer in a dusty hyperluminous quasar
D Farrah, M Baloković, D Stern, K Harris, M Kunimoto, DJ Walton, DM Alexander, P Arévalo, DR Ballantyne, FE Bauer, S Boggs, WN Brandt, M Brightman, F Christensen, DL Clements, W Craig, A Fabian, C Hailey, F Harrison, M Koss, GB Lansbury, B Luo, J Paine, S Petty, K Pitchford, C Ricci, W Zhang
Mar 13, 2017
Mitochondrial DNA sequence characteristics modulate the size of the genetic bottleneck.
Ian J Wilson, Phillipa J Carling, Charlotte L Alston, Vasileios I Floros, Angela Pyle, Gavin Hudson, Suzanne CEH Sallevelt, Costanza Lamperti, Valerio Carelli, Laurence A Bindoff, David C Samuels, Passorn Wonnapinij, Massimo Zeviani, Robert W Taylor, Hubert JM Smeets, Rita Horvath, Patrick F Chinnery
Jan 18, 2016
The $\textit{Nu}$STAR Serendipitous Survey
GB Lansbury, D Stern, J Aird, DM Alexander, C Fuentes, FA Harrison, E Treister, FE Bauer, JA Tomsick, M Baloković, AD Moro, P Gandhi, M Ajello, A Annuar, DR Ballantyne, SE Boggs, WN Brandt, M Brightman, CTJ Chen, FE Christensen, F Civano, A Comastri, WW Craig, K Forster, BW Grefenstette, CJ Hailey, RC Hickox, B Jiang, HD Jun, M Koss, S Marchesi, AD Melo, JR Mullaney, G Noirot, S Schulze, DJ Walton, L Zappacosta, WW Zhang
May 02, 2017
Adults with RRM2B-related mitochondrial disease have distinct clinical and molecular characteristics.
Robert DS Pitceathly, Conrad Smith, Carl Fratter, Charlotte L Alston, Langping He, Kate Craig, Emma L Blakely, Julie C Evans, John Taylor, Zarfishan Shabbir, Marcus Deschauer, Ute Pohl, Mark E Roberts, Matthew C Jackson, Christopher A Halfpenny, Peter D Turnpenny, Peter W Lunt, Michael G Hanna, Andrew M Schaefer, Robert McFarland, Rita Horvath, Patrick F Chinnery, Douglass M Turnbull, Joanna Poulton, Robert W Taylor, Gráinne S Gorman
Mar 07, 2019
Mutations in the nuclear-encoded mitochondrial maintenance gene RRM2B are an important cause of familial mitochondrial disease in both adults and children and represent the third most common cause of multiple mitochondrial DNA...
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