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...

Study of telomere length in men who carry a fragile X premutation or full mutation allele

Human genetics, 2020-12, Vol.139 (12), p.1531-1539

2020

Volltextzugriff (PDF)

Women who carry a fragile X premutation are biologically older than noncarriers as measured by telomere length

American journal of medical genetics. Part A, 2017-11, Vol.173 (11), p.2985-2994

2017

Volltextzugriff (PDF)

Validation and Implementation of the PowerPlex® 16 BIO System STR Multiplex for Forensic Casework

Journal of forensic sciences, 2004-01, Vol.49 (1), p.1-10

2004

Volltextzugriff (PDF)

Detection of a primer-binding site polymorphism for the STR locus D16S539 using the Powerplex 1.1 system and validation of a degenerate primer to correct for the polymorphism

Journal of forensic sciences, 2002-03, Vol.47 (2), p.345-349

2002

Volltextzugriff (PDF)

Clustering of comorbid conditions among women who carry an FMR1 premutation

Genetics in medicine, 2020-04, Vol.22 (4), p.758-766

2020

Volltextzugriff (PDF)

Refining the risk for fragile X–associated primary ovarian insufficiency (FXPOI) by FMR1 CGG repeat size

Genetics in medicine, 2021-09, Vol.23 (9), p.1648-1655

2021

Volltextzugriff (PDF)

Influence of dengue endemicity on malaria identification by automated hematology analyzer - Beckman Coulter LH750: A hospital-based cross-sectional study

Muller journal of medical sciences and research (Mangalore), 2023-01, Vol.14 (1), p.10-15

2023

Volltextzugriff (PDF)

Single-cell expression quantitative trait loci (eQTL) analysis of SLE-risk loci in lupus patient monocytes

Arthritis research & therapy, 2021-11, Vol.23 (1), p.1-290, Article 290

2021

Volltextzugriff (PDF)

Use of DMARDs and biologics during pregnancy and lactation in rheumatoid arthritis: what the rheumatologist needs to know

Therapeutic Advances in Musculoskeletal Disease, 2014-10, Vol.6 (5), p.169-184

2014

Volltextzugriff (PDF)

Clinicopathological Analysis of Whipple’s Pancreaticoduodenectomy Specimens in a Tertiary Care Hospital with Special Emphasis on Grossing

Journal of clinical and diagnostic research, 2021, Vol.15 (1), p.EC01-EC07

2021

Volltextzugriff (PDF)

Translational research of new developments in targeted therapy of colorectal cancer

Pathology, research and practice, 2023-12, Vol.252, p.154888-154888, Article 154888

2023

Volltextzugriff (PDF)

Rheumatoid Arthritis and Pregnancy: Safety Considerations in Pharmacological Management

Drugs (New York, N.Y.), 2011-01, Vol.71 (15), p.1973-1987

2011

Volltextzugriff (PDF)

Predictors of Comorbid Conditions in Women Who Carry an FMR1 Premutation

Frontiers in psychiatry, 2021-10, Vol.12, p.715922

2021

Volltextzugriff (PDF)

Regional european genetic ancestry predicts type I interferon level and risk of severe viral infection

QJM : An International Journal of Medicine, 2024, Vol.117 (8), p.581-588

2024

Volltextzugriff (PDF)

Beyond the exome: What’s next in diagnostic testing for Mendelian conditions

American journal of human genetics, 2023-08, Vol.110 (8), p.1229-1248

2023

Volltextzugriff (PDF)

High Systemic Type I Interferon Activity Is Associated With Active Class III/IV Lupus Nephritis

Journal of rheumatology, 2022-04, Vol.49 (4), p.388-397

2022

Volltextzugriff (PDF)

Development of microextraction methods for the determination of sulfamethoxazole in water and biological samples: modelling, optimization and verification by central composite design

Frontiers in environmental science, 2023-08, Vol.11

2023

Volltextzugriff (PDF)

FXPOI: Pattern of AGG Interruptions Does not Show an Association With Age at Amenorrhea Among Women With a Premutation

Frontiers in genetics, 2018-08, Vol.9, p.292-292

2018

Volltextzugriff (PDF)

Lupus‐Associated Functional Polymorphism in PNP Causes Cell Cycle Abnormalities and Interferon Pathway Activation in Human Immune Cells

Arthritis & rheumatology (Hoboken, N.J.), 2017-12, Vol.69 (12), p.2328-2337

2017

Volltextzugriff (PDF)

Considerations for reporting variants in novel candidate genes identified during clinical genomic testing

Genetics in medicine, 2024-10, Vol.26 (10), p.101199, Article 101199

2024

Volltextzugriff (PDF)

Intra-Arterial Angiolymphoid Hyperplasia with Eosinophilia: A Rare Case Report of Peripheral Medium Sized Muscular Artery Involvement

Journal of clinical and diagnostic research, 2015-08, Vol.9 (8), p.ED16-ED17

2015

Volltextzugriff (PDF)

Type I Interferon Predicts an Alternate Immune System Phenotype in Systemic Lupus Erythematosus

ACR open rheumatology, 2019-10, Vol.1 (8), p.499-506

2019

Volltextzugriff (PDF)

Rheumatoid Arthritis and Pregnancy

Drugs (New York, N.Y.), 2011-10, Vol.71 (15), p.1973-1987

2011

Volltextzugriff (PDF)

Single-cell gene expression patterns in lupus monocytes independently indicate disease activity, interferon and therapy

Lupus science & medicine, 2017-01, Vol.4 (1), p.e000202-e000202

2017

Volltextzugriff (PDF)

Single cell gene expression in lupus patient monocytes reveals a differential impact of interferon signaling between monocyte subtypes (TECH2P.920)

The Journal of immunology (1950), 2015-05, Vol.194 (1_Supplement), p.206-206.30

2015

Volltextzugriff (PDF)

1 – 25 von 29

Suche als RSS-Feed

Aktive Filter

Nur zeigenGeprüft (Peer-Review)

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Mit Volltextzugriff
(26)

Publikationsform

Artikel
(29)

Sprache

Englisch
(29)

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(21)
Science & Technology
(21)
Humans
(8)
Genetics & Heredity
(6)
Rheumatology
(6)
Female
(5)
Alleles
(4)
Fmr1
(4)
Fxpoi
(4)
Lupus
(4)
Mutation
(4)
Ataxia
(3)
Biomedical And Life Sciences
(3)
Biomedicine
(3)
Fragile X Mental Retardation Protein - Genetics
(3)
Fragile X Syndrome
(3)
Fragile X Syndrome - Genetics
(3)
Fxtas
(3)
Gene Expression
(3)
General & Internal Medicine
(3)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Study of telomere length in men who carry a fragile X premutation or full mutation allele

Women who carry a fragile X premutation are biologically older than noncarriers as measured by telomere length

Validation and Implementation of the PowerPlex® 16 BIO System STR Multiplex for Forensic Casework

Detection of a primer-binding site polymorphism for the STR locus D16S539 using the Powerplex 1.1 system and validation of a degenerate primer to correct for the polymorphism

Clustering of comorbid conditions among women who carry an FMR1 premutation

Refining the risk for fragile X–associated primary ovarian insufficiency (FXPOI) by FMR1 CGG repeat size

Influence of dengue endemicity on malaria identification by automated hematology analyzer - Beckman Coulter LH750: A hospital-based cross-sectional study

Single-cell expression quantitative trait loci (eQTL) analysis of SLE-risk loci in lupus patient monocytes

Use of DMARDs and biologics during pregnancy and lactation in rheumatoid arthritis: what the rheumatologist needs to know

Clinicopathological Analysis of Whipple’s Pancreaticoduodenectomy Specimens in a Tertiary Care Hospital with Special Emphasis on Grossing

Translational research of new developments in targeted therapy of colorectal cancer

Rheumatoid Arthritis and Pregnancy: Safety Considerations in Pharmacological Management

Predictors of Comorbid Conditions in Women Who Carry an FMR1 Premutation

Regional european genetic ancestry predicts type I interferon level and risk of severe viral infection

Beyond the exome: What’s next in diagnostic testing for Mendelian conditions

High Systemic Type I Interferon Activity Is Associated With Active Class III/IV Lupus Nephritis

Development of microextraction methods for the determination of sulfamethoxazole in water and biological samples: modelling, optimization and verification by central composite design

FXPOI: Pattern of AGG Interruptions Does not Show an Association With Age at Amenorrhea Among Women With a Premutation

Lupus‐Associated Functional Polymorphism in PNP Causes Cell Cycle Abnormalities and Interferon Pathway Activation in Human Immune Cells

Considerations for reporting variants in novel candidate genes identified during clinical genomic testing

Intra-Arterial Angiolymphoid Hyperplasia with Eosinophilia: A Rare Case Report of Peripheral Medium Sized Muscular Artery Involvement

Type I Interferon Predicts an Alternate Immune System Phenotype in Systemic Lupus Erythematosus

Rheumatoid Arthritis and Pregnancy

Single-cell gene expression patterns in lupus monocytes independently indicate disease activity, interferon and therapy

Single cell gene expression in lupus patient monocytes reveals a differential impact of interferon signaling between monocyte subtypes (TECH2P.920)

Aktive Filter

Suchergebnisse filtern