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...

The Loss of Profilin 1 Causes Early Onset Paget's Disease of Bone

Journal of bone and mineral research, 2020-08, Vol.35 (8), p.1387-1398

2020

Volltextzugriff (PDF)

Novel RPL13 Variants and Variable Clinical Expressivity in a Human Ribosomopathy With Spondyloepimetaphyseal Dysplasia

Journal of bone and mineral research, 2021-02, Vol.36 (2), p.283-297

2021

Volltextzugriff (PDF)

L-plastin associated syndrome of immune deficiency and hematologic cytopenia

Journal of allergy and clinical immunology, 2024-09, Vol.154 (3), p.767-777

2024

Volltextzugriff (PDF)

Society for Maternal-Fetal Medicine Special Statement: Beyond the scalpel: in utero fetal gene therapy and curative medicine

American journal of obstetrics and gynecology, 2021-12, Vol.225 (6), p.B9-B18

2021

Volltextzugriff (PDF)

An LNP-CRISPR gene editing drug demonstrates efficacy and safety in patients with hereditary angioedema following in vivo administration

Journal of allergy and clinical immunology, 2024-08, Vol.154 (2), p.272-274

2024

Volltextzugriff (PDF)

Patient-iPSC-Derived Kidney Organoids Show Functional Validation of a Ciliopathic Renal Phenotype and Reveal Underlying Pathogenetic Mechanisms

American journal of human genetics, 2018-05, Vol.102 (5), p.816-831

2018

Volltextzugriff (PDF)

NanoBiT- and NanoBiT/BRET-based assays allow the analysis of binding kinetics of Wnt-3a to endogenous Frizzled 7 in a colorectal cancer model

British journal of pharmacology, 2023, Vol.181 (20), p.3819-3835

2023

Volltextzugriff (PDF)

Somatic Mutations in TSC1 and TSC2 Cause Focal Cortical Dysplasia

American journal of human genetics, 2017-03, Vol.100 (3), p.454-472

2017

Volltextzugriff (PDF)

Siglec-9 is an inhibitory receptor on human mast cells in vitro

Journal of allergy and clinical immunology, 2023-09, Vol.152 (3), p.711-724.e14

2023

Volltextzugriff (PDF)

Tissue-restricted genome editing in vivo specified by microRNA-repressible anti-CRISPR proteins

RNA (Cambridge), 2019-11, Vol.25 (11), p.1421-1431

2019

Volltextzugriff (PDF)

Sensitization of spinal itch transmission neurons in a mouse model of chronic itch requires an astrocytic factor

Journal of allergy and clinical immunology, 2020-01, Vol.145 (1), p.183-191.e10

2020

Volltextzugriff (PDF)

Improved bacterial RNA-seq by Cas9-based depletion of ribosomal RNA reads

RNA (Cambridge), 2020-08, Vol.26 (8), p.1069-1078

2020

Volltextzugriff (PDF)

Using Human Induced Pluripotent Stem Cell-Derived Organoids to Identify New Pathologies in Patients With PDX1 Mutations

Gastroenterology (New York, N.Y. 1943), 2022-10, Vol.163 (4), p.1053-1063.e7

2022

Volltextzugriff (PDF)

Implementing accelerated dynamics to unravel the effects of high-fidelity Cas9 mutants on target DNA and guide RNA hybrid stability

Journal of biomolecular structure & dynamics, 2023-09, Vol.41 (13), p.6178-6190

2023

Volltextzugriff (PDF)

Melanin Synthesis Pathway Interruption: CRISPR/Cas9-mediated Knockout of dopa decarboxylase (DDC) in Harmonia axyridis (Coleoptera: Coccinellidae)

Journal of insect science (Tucson, Ariz.), 2022-09, Vol.22 (5)

2022

Volltextzugriff (PDF)

Allele-specific editing ameliorates dominant retinitis pigmentosa in a transgenic mouse model

American journal of human genetics, 2021-02, Vol.108 (2), p.295-308

2021

Volltextzugriff (PDF)

Identification of Genes Associated With Hirschsprung Disease, Based on Whole-Genome Sequence Analysis, and Potential Effects on Enteric Nervous System Development

Gastroenterology (New York, N.Y. 1943), 2018-12, Vol.155 (6), p.1908-1922.e5

2018

Volltextzugriff (PDF)

Autism-specific PTEN p.Ile135Leu variant and an autism genetic background combine to dysregulate cortical neurogenesis

American journal of human genetics, 2023-05, Vol.110 (5), p.826-845

2023

Volltextzugriff (PDF)

Integrated analysis of miRNA and mRNA expression profiles in p53-edited PFF cells

Cell cycle (Georgetown, Tex.), 2020-04, Vol.19 (8), p.949-959, Article 949

2020

Volltextzugriff (PDF)

Human iPSC Modeling Reveals Mutation-Specific Responses to Gene Therapy in a Genotypically Diverse Dominant Maculopathy

American journal of human genetics, 2020-08, Vol.107 (2), p.278-292

2020

Volltextzugriff (PDF)

Mutations in the Spliceosome Component CWC27 Cause Retinal Degeneration with or without Additional Developmental Anomalies

American journal of human genetics, 2017-04, Vol.100 (4), p.592-604

2017

Volltextzugriff (PDF)

BMPR2 as a Novel Predisposition Gene for Hereditary Colorectal Polyposis

Gastroenterology (New York, N.Y. 1943), 2023-07, Vol.165 (1), p.162-172.e5

2023

Volltextzugriff (PDF)

Gene editing in allergic diseases: Identification of novel pathways and impact of deleting allergen genes

Journal of allergy and clinical immunology, 2024-07, Vol.154 (1), p.51-58

2024

Volltextzugriff (PDF)

Recapitulating primary immunodeficiencies with expanded potential stem cells: Proof of concept with STAT1 gain of function

Journal of allergy and clinical immunology, 2024-04, Vol.153 (4), p.1125-1139

2024

Volltextzugriff (PDF)

1 – 25 von 69

Suche als RSS-Feed

Aktive Filter

Zeitschrift / SerieMethods In Molecular Biology

KollektionIngentaConnect

KollektionSingle Journals

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(67)
Mit Volltextzugriff
(66)

Publikationsform

Artikel
(68)
Berichte
(1)

Sprache

Englisch
(69)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

The Loss of Profilin 1 Causes Early Onset Paget's Disease of Bone

Novel RPL13 Variants and Variable Clinical Expressivity in a Human Ribosomopathy With Spondyloepimetaphyseal Dysplasia

L-plastin associated syndrome of immune deficiency and hematologic cytopenia

Society for Maternal-Fetal Medicine Special Statement: Beyond the scalpel: in utero fetal gene therapy and curative medicine

An LNP-CRISPR gene editing drug demonstrates efficacy and safety in patients with hereditary angioedema following in vivo administration

Patient-iPSC-Derived Kidney Organoids Show Functional Validation of a Ciliopathic Renal Phenotype and Reveal Underlying Pathogenetic Mechanisms

NanoBiT- and NanoBiT/BRET-based assays allow the analysis of binding kinetics of Wnt-3a to endogenous Frizzled 7 in a colorectal cancer model

Somatic Mutations in TSC1 and TSC2 Cause Focal Cortical Dysplasia

Siglec-9 is an inhibitory receptor on human mast cells in vitro

Tissue-restricted genome editing in vivo specified by microRNA-repressible anti-CRISPR proteins

Sensitization of spinal itch transmission neurons in a mouse model of chronic itch requires an astrocytic factor

Improved bacterial RNA-seq by Cas9-based depletion of ribosomal RNA reads

Using Human Induced Pluripotent Stem Cell-Derived Organoids to Identify New Pathologies in Patients With PDX1 Mutations

Implementing accelerated dynamics to unravel the effects of high-fidelity Cas9 mutants on target DNA and guide RNA hybrid stability

Melanin Synthesis Pathway Interruption: CRISPR/Cas9-mediated Knockout of dopa decarboxylase (DDC) in Harmonia axyridis (Coleoptera: Coccinellidae)

TTC12 Loss-of-Function Mutations Cause Primary Ciliary Dyskinesia and Unveil Distinct Dynein Assembly Mechanisms in Motile Cilia Versus Flagella

Allele-specific editing ameliorates dominant retinitis pigmentosa in a transgenic mouse model

Identification of Genes Associated With Hirschsprung Disease, Based on Whole-Genome Sequence Analysis, and Potential Effects on Enteric Nervous System Development

Autism-specific PTEN p.Ile135Leu variant and an autism genetic background combine to dysregulate cortical neurogenesis

Integrated analysis of miRNA and mRNA expression profiles in p53-edited PFF cells

Human iPSC Modeling Reveals Mutation-Specific Responses to Gene Therapy in a Genotypically Diverse Dominant Maculopathy

Mutations in the Spliceosome Component CWC27 Cause Retinal Degeneration with or without Additional Developmental Anomalies

BMPR2 as a Novel Predisposition Gene for Hereditary Colorectal Polyposis

Gene editing in allergic diseases: Identification of novel pathways and impact of deleting allergen genes

Recapitulating primary immunodeficiencies with expanded potential stem cells: Proof of concept with STAT1 gain of function

Aktive Filter

Suchergebnisse filtern