UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani family

Human molecular genetics, 2014-11, Vol.23 (22), p.5940-5949

2014

Volltextzugriff (PDF)

Initiation or switch to insulin degludec/insulin aspart in adults with type 2 diabetes in India: Results from a prospective, non-interventional, real-world study

Journal of family medicine and primary care, 2024-09, Vol.13 (9), p.3590-3597

2024

Volltextzugriff (PDF)

Identification of a novel protein truncating mutation p.Asp98 in XPC associated with xeroderma pigmentosum in a consanguineous Pakistani family

Molecular genetics & genomic medicine, 2020-02, Vol.8 (2), p.e1060-n/a

2020

Volltextzugriff (PDF)

Identification of a novel homozygous TRAPPC9 gene mutation causing non‐syndromic intellectual disability, speech disorder, and secondary microcephaly

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2017-12, Vol.174 (8), p.839-845

2017

Volltextzugriff (PDF)

Feminism in the Select Novels of Kamala Markandaya

Language in India, 2019-04, Vol.19 (4), p.202

2019

Volltextzugriff (PDF)

Bortezomib-mediated downregulation of S-phase kinase protein-2 (SKP2) causes apoptotic cell death in chronic myelogenous leukemia cells

Journal of translational medicine, 2016-03, Vol.14 (69), p.69-69, Article 69

2016

Volltextzugriff (PDF)

Molecular outcomes, clinical consequences, and genetic diagnosis of Oculocutaneous Albinism in Pakistani population

Scientific reports, 2017-03, Vol.7 (1), p.44185-44185, Article 44185

2017

Volltextzugriff (PDF)

Abstract 4: Derived time-in-range is associated with major adverse cardiovascular event in T2D: Data from the DEVOTE trial

Indian journal of endocrinology and metabolism, 2022-03, Vol.26 (Suppl 1), p.S6-S7

2022

Volltextzugriff (PDF)

Integrated Mechanism of Routing and Key Exchange in AODV

WSEAS Transactions on Communications, 2007-04, Vol.6 (4), p.565-572

2007

Volltextzugriff (PDF)

Abstract 28: Change in glycaemic parameters in adults with type 2 diabetes initiated with or switched to insulin degludec/insulin aspart (IDegAsp) in a real-world setting – An analysis of Indian cohort of ARISE study

Indian journal of endocrinology and metabolism, 2022-03, Vol.26 (Suppl 1), p.S15-S16

2022

Volltextzugriff (PDF)

A novel deletion mutation in the TUSC3 gene in a consanguineous Pakistani family with autosomal recessive nonsyndromic intellectual disability

BMC medical genetics, 2011-04, Vol.12 (1), p.56-56, Article 56

2011

Volltextzugriff (PDF)

Cardiac Disorder Classification by Electrocardiogram Sensing Using Deep Neural Network

Complexity (New York, N.Y.), 2021, Vol.2021 (1)

2021

Volltextzugriff (PDF)

A level set based fractional order variational model for motion estimation in application oriented spectrum

Expert systems with applications, 2023-06, Vol.219, p.119628, Article 119628

2023

Volltextzugriff (PDF)

Arrhythmia Classification Techniques Using Deep Neural Network

Complexity (New York, N.Y.), 2021, Vol.2021 (1)

2021

Volltextzugriff (PDF)

Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability

American journal of human genetics, 2012-05, Vol.90 (5), p.856-863

2012

Volltextzugriff (PDF)

Post-polymerization modification reactions of poly(glycidyl methacrylate)s

RSC advances, 2017-01, Vol.7 (88), p.55874-55884

2017

Volltextzugriff (PDF)

Charbonnier-Marchaud Based Fractional Variational Model for Motion Estimation in Multispectral Vision System

Journal of physics. Conference series, 2022-08, Vol.2327 (1), p.12031

2022

Volltextzugriff (PDF)

ECG Images dataset of Cardiac and COVID-19 Patients

Data in brief, 2021-02, Vol.34, p.106762-106762, Article 106762

2021

Volltextzugriff (PDF)

Chronic Ulnar Shaft Stress Injury in an IndyCar Pit Crew Member: A Clinical Vignette

American journal of physical medicine & rehabilitation, 2024-02, Vol.103 (2), p.e12

2024

Volltextzugriff (PDF)

Artificial neural networks for the prediction of biochar yield: A comparative study of metaheuristic algorithms

Bioresource technology, 2022-07, Vol.355, p.127215-127215, Article 127215

2022

Volltextzugriff (PDF)

A nonlinear modeling of fractional order based variational model in optical flow estimation

Optik (Stuttgart), 2022-07, Vol.261, p.169136, Article 169136

2022

Volltextzugriff (PDF)

Aspirin Resistance in Vascular Disease: A Review Highlighting the Critical Need for Improved Point-of-Care Testing and Personalized Therapy

International journal of molecular sciences, 2022-10, Vol.23 (19), p.11317

2022

Volltextzugriff (PDF)

Brain Tumor Analysis Empowered with Deep Learning: A Review, Taxonomy, and Future Challenges

Brain sciences, 2020-02, Vol.10 (2), p.118

2020

Volltextzugriff (PDF)

UNLOCKING THE GENETIC MYSTERIES OF SARS-COV-2: A DEEP DIVE INTO THE SEQUENCE, STRUCTURE AND DYNAMICS OF MPRO MUTATIONS

Biochemical and cellular archives, 2024-01, Vol.24 (1)

Khan, Mohd Muzammil

2024

Volltextzugriff (PDF)

In-silico approaches for identification of compounds inhibiting SARS-CoV-2 3CL protease

PloS one, 2023-04, Vol.18 (4), p.e0284301-e0284301

2023

Volltextzugriff (PDF)

1 – 25 von 808

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(452)
Mit Volltextzugriff
(652)

Publikationsform

Sprache

Englisch
(807)
Arabisch
(3)

Erscheinungsjahr

n.n

Thema

Science & Technology
(326)
Life Sciences & Biomedicine
(203)
Technology
(95)
Humans
(79)
Physical Sciences
(56)
Engineering
(52)
General & Internal Medicine
(50)
Computer Science
(47)
Medicine, General & Internal
(46)
Male
(41)
Mutation
(36)
Proteins
(36)
Genetics & Heredity
(32)
Pakistan
(31)
Algorithms
(29)
Chemistry
(29)
Machine Learning
(29)
Patients
(29)
Female
(27)
Computer Science, Information Systems
(26)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani family

Initiation or switch to insulin degludec/insulin aspart in adults with type 2 diabetes in India: Results from a prospective, non-interventional, real-world study

Identification of a novel protein truncating mutation p.Asp98 in XPC associated with xeroderma pigmentosum in a consanguineous Pakistani family

Identification of a novel homozygous TRAPPC9 gene mutation causing non‐syndromic intellectual disability, speech disorder, and secondary microcephaly

Feminism in the Select Novels of Kamala Markandaya

Bortezomib-mediated downregulation of S-phase kinase protein-2 (SKP2) causes apoptotic cell death in chronic myelogenous leukemia cells

Molecular outcomes, clinical consequences, and genetic diagnosis of Oculocutaneous Albinism in Pakistani population

Abstract 4: Derived time-in-range is associated with major adverse cardiovascular event in T2D: Data from the DEVOTE trial

Integrated Mechanism of Routing and Key Exchange in AODV

Abstract 28: Change in glycaemic parameters in adults with type 2 diabetes initiated with or switched to insulin degludec/insulin aspart (IDegAsp) in a real-world setting – An analysis of Indian cohort of ARISE study

A novel deletion mutation in the TUSC3 gene in a consanguineous Pakistani family with autosomal recessive nonsyndromic intellectual disability

Cardiac Disorder Classification by Electrocardiogram Sensing Using Deep Neural Network

A level set based fractional order variational model for motion estimation in application oriented spectrum

Arrhythmia Classification Techniques Using Deep Neural Network

Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability

Post-polymerization modification reactions of poly(glycidyl methacrylate)s

Charbonnier-Marchaud Based Fractional Variational Model for Motion Estimation in Multispectral Vision System

ECG Images dataset of Cardiac and COVID-19 Patients

Chronic Ulnar Shaft Stress Injury in an IndyCar Pit Crew Member: A Clinical Vignette

Artificial neural networks for the prediction of biochar yield: A comparative study of metaheuristic algorithms

A nonlinear modeling of fractional order based variational model in optical flow estimation

Aspirin Resistance in Vascular Disease: A Review Highlighting the Critical Need for Improved Point-of-Care Testing and Personalized Therapy

Brain Tumor Analysis Empowered with Deep Learning: A Review, Taxonomy, and Future Challenges

UNLOCKING THE GENETIC MYSTERIES OF SARS-COV-2: A DEEP DIVE INTO THE SEQUENCE, STRUCTURE AND DYNAMICS OF MPRO MUTATIONS

In-silico approaches for identification of compounds inhibiting SARS-CoV-2 3CL protease

Suchergebnisse filtern