Results 91 to 100 of about 98,982 (312)

WEHRMACHTGEFÄNGNIS (WG) ANKLAM

, 2022
WG Anklam was mentioned in official documentation as early as November 1938, albeit with the additional designation “Zwischenunterkunft Glatz” (today Kłodzko, Poland).1 The provisional unit in Glatz became necessary because the prison in Anklam, which had originally been intended as a women’s detention center, would only be available in late 1940 due ...
openaire   +1 more source

Mapping stool reads against BSI whole genome sequences (WGS).

, 2023
Each available BSI isolate was subjected to whole genome shotgun sequencing and then assembly into WGS (mean 97.49% coverage; mean 78.81X depth). Stool short reads were then aligned with multiple genomes (indicated on the left of the graph), which ...
Laurel J. Glaser (17125014), Jevon Graham-Wooten (10919497), Frederic D. Bushman (22634), Christopher H. Gu (9617720), Layla A. Khatib (17125002), Ayannah S. Fitzgerald (17125005), Caroline A. Ittner (17125008), YuChung Chuang (17125011), Nuala J. Meyer (12189380), Scott Sherrill-Mix (692150), Ronald G. Collman (10273052)   +10 more
core   +1 more source

Patient and Family Reported Clinical Picture of IRF2BPL‐Related Disorders

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT IRF2BPL‐related disorder is a neurodevelopmental disorder caused by heterozygous variants in the IRF2BPL (Interferon Regulatory Factor 2 Binding Protein‐Like) gene. The few reports available in the literature suggest that common symptoms include developmental delay, intellectual disability, and developmental regression.
Zoe Goldstone‐Joubert, Danielle M. Pascual, Laurie Anne Bailey, Loren D. M. Peña, Paul C. Marcogliese   +4 more
wiley   +1 more source

Prenatal Evaluation of RNU4‐2 Variants in Fetuses With Central Nervous System Anomalies

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Fetal central nervous system (CNS) anomalies are among the most common congenital malformations, yet the overall prenatal diagnostic yield of current genetic testing remains below 40%. Variants in RNU4‐2, a non‐coding gene encoding the U4 small nuclear RNA (snRNA), have recently been linked to a novel highly recurrent dominant ...
Yiyao Chen, Li Gao, Xu Han, Yunyun Cao, Lanlan Zhang, Yi Wu, Xinrong Zhao, Wenjing Hu, Ruiyu Ma, Renyi Hua, Niu Li, Yanlin Wang, Jian Wang, Shuyuan Li   +13 more
wiley   +1 more source

Investigation of a Carbapenemase-producing Acinetobacter baumannii outbreak using whole genome sequencing versus a standard epidemiologic investigation

Antimicrobial Resistance and Infection Control, 2018
Background The standard epidemiologic investigation of outbreaks typically relies on spatiotemporal data and pulsed-field gel electrophoresis (PFGE), but whole genome sequencing (WGS) is becoming increasingly used.
Chloe Bogaty, Laura Mataseje, Andrew Gray, Brigitte Lefebvre, Simon Lévesque, Michael Mulvey, Yves Longtin   +6 more
doaj   +1 more source

A rhesus macaque model of α‐dystroglycanopathy caused by a POMT1 splice altering variant

Animal Models and Experimental Medicine, EarlyView.
Rhesus macaques homozygous for a naturally occurring spice altering variant in the POMT1 gene develop lissencephaly, microphthalmia, and muscular contracture. The presentation models severe presentation of the human Walker‐Warburg syndrome. Abstract Background Biallelic mutations in genes associated with α‐dystroglycan glycosylation manifest in a ...
Anya Nordlund, Brian LaMendola, Nathan P. Crilly, Seth Kittle, Betsy M. Ferguson, Anne D. Lewis, Jeff Wall, Samuel M. Peterson   +7 more
wiley   +1 more source

Genetic Modifiers of ABCA1 Activity Interact with APOE Isoforms to Mediate Alzheimer's Disease Risk

Annals of Neurology, EarlyView.
Objective ATP‐binding cassette transporter A1 (ABCA1) has been associated with Alzheimer's disease (AD), but the mechanisms by which it impacts disease risk are unknown. ABCA1 is known to bind apolipoprotein E (ApoE) and catalyze apolipoprotein lipidation.
Andrés Peña‐Tauber, Ricardo Hernández Arriaza, Dylan Reil, Manon Muntaner, Junyoung Park, Benjamin Grenier‐Boley, Marc Hulsman, Philippe Amouyel, Céline Bellenguez, Camille Charbonnier, Jean‐François Deleuze, Orio Dols‐Icardo, John Hardy, Henne Holstege, Gaël Nicolas, Simon Mead, Michael Wagner, Alfredo Ramirez, Rebecca Sims, John van Swieten, Julie Willams, Jean‐Charles Lambert, Chaitan Khosla, Yann Le Guen, Michael D Greicius   +24 more
wiley   +1 more source

A Validation Approach of an End-to-End Whole Genome Sequencing Workflow for Source Tracking of Listeria monocytogenes and Salmonella enterica

Frontiers in Microbiology, 2018
Whole genome sequencing (WGS), using high throughput sequencing technology, reveals the complete sequence of the bacterial genome in a few days. WGS is increasingly being used for source tracking, pathogen surveillance and outbreak investigation due to ...
Anne-Catherine Portmann, Coralie Fournier, Johan Gimonet, Catherine Ngom-Bru, Caroline Barretto, Leen Baert   +5 more
doaj   +1 more source

WEHRMACHTGEFÄNGNIS (WG) GERMERSHEIM

, 2022
On September 9, 1936, the German Army High Command (Oberkommando des Heeres, OKH) issued an order for the former detention facility of the Germersheim fortress, built between 1834 and 1861, to be expanded to serve as a military prison for the Wehrmacht (map 4d).
openaire   +1 more source

Econometric analyses of microfinance credit group formation, contractual risks and welfare impacts in Northern Ethiopia [PDF]

, 2009
Key words Microfinance, joint liability, contractual risk, group formation, risk-matching, impact evaluation, Panel data econometrics, dynamic panel probit, trend models, fixed-effects, composite counterfactuals, propensity score matching, farm ...
Berhane Tesfay, G.
core