№ files_lp_4_process_1_52466
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The document is a systematic review examining the genetic variants associated with Alzheimer disease across the 22 Arab countries, focusing on genetic markers and clinical phenotypes in various populations.
Note:
Year
Topic:
Genetic Variants, Alzheimer Disease, Arab Countries
Document Type:
Systematic Review
Institution:
Qatar University
Author:
Hissa Faleh Al-Thani, Muneera Naseer Ahmad, Salma Younes, Hatem Zayed
Target Audience:
Researchers, Healthcare Professionals
Price: 8 / 10 USD
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The product description is provided for reference. Actual content and formatting may differ slightly.
Subject:
Biology
Topic:
Genetic variants and phenotypes
Key concepts:
Mutation, gene transcription, translation, protein synthesis, RNA polymerase binding, amino acid sequence
Curriculum references:
SB3.9B; SB3.10B
Document type:
Lesson plan
Educational level:
Secondary education
Components:
Objectives; Learning outcomes; Quick Quiz; Starters; Exploring activities; Worksheets; Safety guidance; Equipment list
Resources referenced:
ALDS presentation SB3e Genetic variants and phenotypes objectives; ALDS presentation SB3e Quick Quiz; Worksheet SB3e.1; Worksheet SB3e.2; Student Book SB3d Protein synthesis
Assessment methods:
Quick Quiz; Progression questions; Confidence level scoring; Peer checking activity
Practical activities:
Protein modelling with beads; Genetic code transcription and translation exercise
Safety considerations:
Eye protection required; Slip hazard from dropped beads
Document type:
Supplemental table
Subject:
Summary of nominated genetic variants per gene
Content:
Gene symbols, HGNC Gene IDs, number of variants nominated, associated disorders, ACMG 73 List status
Referenced policy:
ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing
Referenced organization:
American College of Medical Genetics and Genomics (ACMG)
Referenced publication:
Genet Med (2021)
Authors of referenced policy:
Miller, D.T.; Lee, K.; Chung, W.K.; et al.
Notes:
Includes annotations regarding multi-gene deletions or fusions and dual submissions to variant curation expert panels
Note:
Year
Year:
2026
Note:
Region / city
Topic:
Biotechnology, Enzymatic Variants
Document Type:
Supplementary Material
Author:
Hanna Englert, Josephine Göbel, Danika Khong, Maryam Omidi, Nina Wolska, Sandra Konrath, Maike Frye, Reiner K. Mailer, Manu Beerens, Julian C. Gerwers, Roger J. S. Preston, Jacob Odeberg, Lynn M. Butler, Coen Maas, Evi X. Stavrou, Tobias A. Fuchs, Thomas Renné
Target Audience:
Researchers, Biotechnologists
Description:
A supplementary document detailing the analysis of novel enzymatic variants targeting NETs, including protein sequence alignments and statistical comparisons.
Note:
Year
Topic:
Structural Variants, Genome Analysis
Document Type:
Scientific Figures
Target Audience:
Researchers, Geneticists
Year:
2023
Region / City:
N/A
Theme:
Genetics / Variant Interpretation
Document Type:
Table
Institution:
PreventionGenetics
Author:
N/A
Target Audience:
Geneticists, Researchers
Period of Validity:
N/A
Approval Date:
N/A
Date of Changes:
N/A
Year:
2026
Region / City:
Not specified
Topic:
Genomics, SNP Variants
Document Type:
Research Supplement
Author:
Not specified
Target Audience:
Researchers, Genomics Professionals
Period of Validity:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
Not specified
Region:
Not specified
Subject:
Authentication security, passkeys, FIDO2, Cognitive DOM, intent-aware access control
Document type:
Analytical comparison and product positioning brief
Organizations referenced:
FIDO Alliance, Apple, Google, Microsoft
Technologies referenced:
FIDO2, WebAuthn, Windows Hello, Apple Touch ID, Apple Face ID, Android biometrics, iCloud Keychain, Google Password Manager
Product:
xAuth.ai
Comparative scope:
FIDO2 roaming security keys, platform passkeys, synced passkeys, enterprise-managed passkeys, raw WebAuthn/FIDO2 implementations
Security concepts:
phishing resistance, hardware-bound credentials, biometric authentication, DOM telemetry, automation detection, risk scoring, friction-on-failure (FOF), high-value access management (HVAM)
Intended audience:
CISOs, enterprise security architects, SOC teams, insurers, auditors, procurement and technical leadership
Authors:
Jasmine Gratton; Steve E Humphries; Marta Futema
Institutions:
Institute of Cardiovascular Science, Faculty of Population Health Sciences, University College London, London, United Kingdom; Cardiology Research Centre, Molecular and Clinical Sciences Research Institute, St George’s University of London, London, United Kingdom
Country:
United Kingdom
Data source:
UK Biobank
Study design:
Population-based cohort study
Subject:
Prevalence of FH-causing genetic variants and association with LDL-C levels across ancestry groups
Population:
European, South Asian, and African ancestry participants
Sample size:
140,439 European; 4,067 South Asian; 3,906 African participants with lipid and whole exome sequencing data
Genes analysed:
LDLR; APOB; PCSK9
Methods:
Principal component analysis; whole exome sequencing; variant classification using ACMG guidelines
Outcome measures:
Prevalence of pathogenic and likely pathogenic FH variants; LDL-C concentration adjusted for statin use; prevalence and incidence of coronary heart disease
Period of data collection:
2006–2010
Ethical approval:
Conducted under approved UK Biobank application 40721
Type of document:
Scientific research article
Year:
Not specified
Subject:
English language
Grade:
10
Educational programme:
Spotlight
Type of document:
Written test
Assessment type:
Entrance control work
Structure:
Multiple-choice tasks and word-formation tasks
Number of variants:
2
Number of tasks per variant:
45
Sections:
Part 1 (multiple choice), Part 2 (word formation)
Answer key:
Included
Target audience:
Grade 10 students
Year:
2023
Region / City:
Unknown
Topic:
Cancer Research, Pharmacogenetics
Document Type:
Research Supplementary Material
Organization / Institution:
Unknown
Author:
Unknown
Target Audience:
Researchers, Medical Professionals
Period of Validity:
Ongoing
Approval Date:
Unknown
Modification Date:
Unknown
Year:
2026
Event:
3GPP TSG‑WG SA2#173
Location:
Goa
Country:
India
Dates:
9–13 February 2026
Working Group:
3GPP SA2
Standardization Body:
3rd Generation Partnership Project
Source Organizations:
ZTE; InterDigital
Pen-holder(s):
ZTE; InterDigital
Work Item:
FS_6G_ARC
Agenda Item:
20.6.2
Document Type:
Technical contribution
Topic:
6G Service-Based Architecture (SBA) framework and solution variants
Subject Area:
Network function registration, discovery, selection, and architecture evolution for 6G core networks
Purpose:
Approval
Content Structure:
High-level summary table of solution variants and detailed description of enhancements to NF profiles and discovery procedures
Year:
1982
Manufacturer:
Lesney Products & Co. Ltd
Scale:
1:62
Length:
78 mm
Width:
30 mm
Height:
21 mm
Material:
Metal base, plastic interior, black plastic wheels with silver hubs
Lettering:
MATCHBOX bold italic in frame
Model Number:
LS 12-E / LS 51-E
Pre-production Variants:
Yes
Country Codes:
USA (MB 12-E, MB 51-E), UK (51F), ROW (51)
Box Types:
L, Ger-B, M, Win-A
Production Notes:
MAN number 051 allocated in 1982
Year:
2026
Region / City:
Goa, India
Topic:
Solutions, 6G, ARC
Document Type:
Contribution for approval
Organization:
3GPP TSG-WG SA2
Author:
Pen-holder(s)
Target Audience:
3GPP Working Group
Period of Validity:
N/A
Approval Date:
February 2026
Date of Changes:
N/A
Year:
2026
Region / City:
Houston, TX; Warsaw, Poland; Phoenix, AZ; New York, NY; Bogota, Columbia; Austin, TX; Indianapolis, IN; Spokane, WA; Parkville VIC, Australia
Topic:
Genomic disorders, Mendelian traits, NAHR-mediated copy-number variants
Document Type:
Research Article
Institution / Organization:
Baylor College of Medicine, University of Warsaw, Warsaw University of Technology, Phoenix Children’s Hospital, Lenox Hill Hospital, Instituto de Referencia Andino, Signature Genomic Laboratories, Murdoch Children’s Research Institute
Author:
Piotr Dittwald, Tomasz Gambin, Przemyslaw Szafranski, Jian Li, Stephen Amato, Michael Y. Divon, Lisa Ximena Rodríguez Rojas, Lindsay E. Elton, Daryl A. Scott, Christian P. Schaaf, Wilfredo Torres-Martinez, Abby K. Stevens, Jill A. Rosenfeld, Satish Agadi, David Francis, Sung-Hae L. Kang, Amy Breman, Seema R. Lalani, Carlos A. Bacino, Weimin Bi, Aleksandar Milosavljevic, Arthur L. Beaudet, Ankita Patel, Chad A. Shaw, James R. Lupski, Anna Gambin, Sau Wai Cheung, Pawel Stankiewicz
Target Audience:
Medical and clinical geneticists, researchers in genomic disorders
Period of Action:
N/A
Approval Date:
N/A
Date of Modifications:
N/A
Year:
2023
Region / City:
Egypt
Theme:
Human rights, Death penalty
Document Type:
Joint Submission
Organization / Institution:
Reprieve, The Advocates for Human Rights
Author:
Reprieve, The Advocates for Human Rights
Target Audience:
United Nations Committee on the Rights of the Child
Period of Validity:
N/A
Approval Date:
July 2023
Date of Changes:
N/A
Year:
2025
Region / City:
United Arab Emirates
Topic:
Common Reporting Standard, Financial Information Exchange
Document Type:
FAQ
Authority / Organization:
Ministry of Finance, United Arab Emirates
Author:
Not specified
Target Audience:
Financial Institutions, Tax Authorities
Period of Validity:
Indefinite
Approval Date:
June 2025
Amendment Date:
Not specified
Year:
2025
Region / city:
Arab States
Thematic area:
Anti-corruption, Governance
Document type:
Evaluation Report
Organ / institution:
United Nations Development Programme (UNDP)
Author:
Andrei Iovu, PhD
Target audience:
UNDP Regional Bureau for Arab States, KOICA, participating governments, development partners
Period of action:
November 2019 - June 2025
Approval date:
July 7th, 2025
Date of changes:
June 2025
Year:
2025
Region / City:
Syrian Arab Republic
Topic:
Human rights violations, political transitions
Document type:
Report
Institution:
United Nations Human Rights Council
Author:
Independent International Commission of Inquiry on the Syrian Arab Republic
Target audience:
United Nations, policymakers, human rights organizations
Period of validity:
December 2024 - January 2025
Approval date:
14 March 2025
Amendment date:
Not specified