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...

Tmem30a deficiency leads to retinal rod bipolar cell degeneration

Journal of neurochemistry, 2019-02, Vol.148 (3), p.400-412

2019

Volltextzugriff (PDF)

Loss of the ER membrane protein complex subunit Emc3 leads to retinal bipolar cell degeneration in aged mice

PloS one, 2020-09, Vol.15 (9), p.e0238435-e0238435

2020

Volltextzugriff (PDF)

Deletion of the Impg2 gene causes the degeneration of rod and cone cells in mice

Human molecular genetics, 2020-06, Vol.29 (10), p.1624-1634

2020

Volltextzugriff (PDF)

Mettl14-mediated m6A modification is essential for visual function and retinal photoreceptor survival

BMC biology, 2022-06, Vol.20 (1), p.140-140, Article 140

2022

Volltextzugriff (PDF)

TMEM30A deficiency in endothelial cells impairs cell proliferation and angiogenesis

Journal of cell science, 2019-04, Vol.132 (7)

2019

Volltextzugriff (PDF)

Three-Party Password Authentication and Key Exchange Protocol Based on MLWE

Symmetry (Basel), 2023-09, Vol.15 (9), p.1750

2023

Volltextzugriff (PDF)

Tmem30a Plays Critical Roles in Ensuring the Survival of Hematopoietic Cells and Leukemia Cells in Mice

The American journal of pathology, 2018-06, Vol.188 (6), p.1457-1468

2018

Volltextzugriff (PDF)

Loss of phosphatidylserine flippase β-subunit Tmem30a in podocytes leads to albuminuria and glomerulosclerosis

Disease models & mechanisms, 2021-06, Vol.14 (6)

2021

Volltextzugriff (PDF)

Hepatic Tmem30a Deficiency Causes Intrahepatic Cholestasis by Impairing Expression and Localization of Bile Salt Transporters

The American journal of pathology, 2017-12, Vol.187 (12), p.2775-2787

2017

Volltextzugriff (PDF)

Defective EMC1 drives abnormal retinal angiogenesis via Wnt/β-catenin signaling and may be associated with the pathogenesis of familial exudative vitreoretinopathy

Genes & diseases, 2023-11, Vol.10 (6), p.2572-2585

2023

Volltextzugriff (PDF)

A missense mutation in Pitx2 leads to early-onset glaucoma via NRF2-YAP1 axis

Cell death & disease, 2021-10, Vol.12 (11), p.1017-1017, Article 1017

2021

Volltextzugriff (PDF)

The endoplasmic reticulum membrane protein complex subunit Emc6 is essential for rhodopsin localization and photoreceptor cell survival

Genes & diseases, 2024-03, Vol.11 (2), p.1035-1049

2024

Volltextzugriff (PDF)

Disruption of Tmem30a results in cerebellar ataxia and degeneration of Purkinje cells

Cell death & disease, 2018-09, Vol.9 (9), p.899-13, Article 899

2018

Volltextzugriff (PDF)

Loss of Tmem30a leads to photoreceptor degeneration

Scientific reports, 2017-08, Vol.7 (1), p.9296-14, Article 9296

2017

Volltextzugriff (PDF)

CTNND1 variants cause familial exudative vitreoretinopathy through Wnt/Cadherin axis

JCI insight, 2022-07, Vol.7 (14)

2022

Volltextzugriff (PDF)

Targeted Next-Generation Sequencing Reveals Novel RP1 Mutations in Autosomal Recessive Retinitis Pigmentosa

Genetic testing and molecular biomarkers, 2018-02, Vol.22 (2), p.109-114

2018

Volltextzugriff (PDF)

Dialect competence, dialect attitude and social inclusion: A case study of migrants in Chongqing, China

International multilingual research journal, 2023-10, Vol.17 (4), p.318-332

2023

Volltextzugriff (PDF)

Deletion of Asrgl1 Leads to Photoreceptor Degeneration in Mice

Frontiers in cell and developmental biology, 2022-01, Vol.9, p.783547-783547

2022

Volltextzugriff (PDF)

Dysregulated m6A modification promotes lipogenesis and development of non-alcoholic fatty liver disease and hepatocellular carcinoma

Molecular therapy, 2022-06, Vol.30 (6), p.2342-2353

2022

Volltextzugriff (PDF)

Politeness in Professional Contexts Edited by Dawn Archer, Karen Grainger, and Piotr Jagodzinski (2020)

East Asian Pragmatics, 2022-06, Vol.7 (2)

Yang, Yeming

2022

Volltextzugriff (PDF)

The phosphatidylserine flippase β-subunit Tmem30a is essential for normal insulin maturation and secretion

Molecular therapy, 2021-09, Vol.29 (9), p.2854-2872

2021

Volltextzugriff (PDF)

LMBR1L regulates the proliferation and migration of endothelial cells through Norrin/β-catenin signaling

Journal of cell science, 2022-03, Vol.135 (6)

2022

Volltextzugriff (PDF)

Catenin α 1 mutations cause familial exudative vitreoretinopathy by overactivating Norrin/β-catenin signaling

The Journal of clinical investigation, 2021-03, Vol.131 (6), p.1-18

2021

Volltextzugriff (PDF)

Specific ablation of Hippo signalling component Yap1 in retinal progenitors and Müller cells results in late onset retinal degeneration

Journal of cellular physiology, 2022-06, Vol.237 (6), p.2673-2689

2022

Volltextzugriff (PDF)

CAGAN: Constrained neural architecture search for GANs

Knowledge-based systems, 2024-10, Vol.302, p.112277, Article 112277

2024

Volltextzugriff (PDF)

1 – 25 von 231

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(189)
Mit Volltextzugriff
(201)

Publikationsform

Sprache

Englisch
(216)
Chinesisch
(18)

Erscheinungsjahr

n.n

Thema

Science & Technology
(155)
Life Sciences & Biomedicine
(73)
Technology
(59)
Physical Sciences
(37)
Humans
(35)
Engineering
(26)
Female
(26)
Male
(24)
Materials Science
(23)
Animals
(19)
Middle Aged
(18)
Mutation
(18)
Chemistry
(17)
Retina
(17)
Genetics & Heredity
(16)
Biochemistry & Molecular Biology
(15)
Materials Science, Multidisciplinary
(15)
Mice
(15)
Science & Technology - Other Topics
(15)
Adult
(14)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

Tmem30a deficiency leads to retinal rod bipolar cell degeneration

Loss of the ER membrane protein complex subunit Emc3 leads to retinal bipolar cell degeneration in aged mice

Deletion of the Impg2 gene causes the degeneration of rod and cone cells in mice

Mettl14-mediated m6A modification is essential for visual function and retinal photoreceptor survival

TMEM30A deficiency in endothelial cells impairs cell proliferation and angiogenesis

Three-Party Password Authentication and Key Exchange Protocol Based on MLWE

Tmem30a Plays Critical Roles in Ensuring the Survival of Hematopoietic Cells and Leukemia Cells in Mice

Loss of phosphatidylserine flippase β-subunit Tmem30a in podocytes leads to albuminuria and glomerulosclerosis

Hepatic Tmem30a Deficiency Causes Intrahepatic Cholestasis by Impairing Expression and Localization of Bile Salt Transporters

Defective EMC1 drives abnormal retinal angiogenesis via Wnt/β-catenin signaling and may be associated with the pathogenesis of familial exudative vitreoretinopathy

A missense mutation in Pitx2 leads to early-onset glaucoma via NRF2-YAP1 axis

The endoplasmic reticulum membrane protein complex subunit Emc6 is essential for rhodopsin localization and photoreceptor cell survival

Disruption of Tmem30a results in cerebellar ataxia and degeneration of Purkinje cells

Loss of Tmem30a leads to photoreceptor degeneration

CTNND1 variants cause familial exudative vitreoretinopathy through Wnt/Cadherin axis

Targeted Next-Generation Sequencing Reveals Novel RP1 Mutations in Autosomal Recessive Retinitis Pigmentosa

Dialect competence, dialect attitude and social inclusion: A case study of migrants in Chongqing, China

Deletion of Asrgl1 Leads to Photoreceptor Degeneration in Mice

Dysregulated m6A modification promotes lipogenesis and development of non-alcoholic fatty liver disease and hepatocellular carcinoma

Politeness in Professional Contexts Edited by Dawn Archer, Karen Grainger, and Piotr Jagodzinski (2020)

The phosphatidylserine flippase β-subunit Tmem30a is essential for normal insulin maturation and secretion

LMBR1L regulates the proliferation and migration of endothelial cells through Norrin/β-catenin signaling

Catenin α 1 mutations cause familial exudative vitreoretinopathy by overactivating Norrin/β-catenin signaling

Specific ablation of Hippo signalling component Yap1 in retinal progenitors and Müller cells results in late onset retinal degeneration

CAGAN: Constrained neural architecture search for GANs

Suchergebnisse filtern