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...

Cellular mechanisms of connexin-based inherited diseases

Trends in cell biology, 2022-01, Vol.32 (1), p.58-69

2022

Volltextzugriff (PDF)

Tricellular adherens junctions provide a cell surface delivery platform for connexin 26/30 oligomers in the cochlea

Hearing research, 2021-02, Vol.400, p.108137-108137, Article 108137

2021

Volltextzugriff (PDF)

Heart and liver connexin expression related to the first stage of aging: A study on naturally aged animals

Acta histochemica, 2020-12, Vol.122 (8), p.151651-151651, Article 151651

2020

Volltextzugriff (PDF)

Identification of homozygous mutations for hearing loss

Gene, 2021-04, Vol.778, p.145464-145464, Article 145464

2021

Volltextzugriff (PDF)

Generation of hiPSC line UMi030-A from an individual with the hearing loss-related GJB2 mutation c.109G > A

Stem cell research, 2022-01, Vol.58, p.102599-102599, Article 102599

2022

Volltextzugriff (PDF)

Computational Studies of Molecular Permeation through Connexin26 Channels

Biophysical journal, 2016-02, Vol.110 (3), p.584-599

2016

Volltextzugriff (PDF)

The p.Gly130Val mutation in the GJB2 gene: A familiar case of autosomal dominant non-syndromic hearing loss

International journal of pediatric otorhinolaryngology, 2019-12, Vol.127, p.109653-109653, Article 109653

2019

Volltextzugriff (PDF)

Deconstruction of the human connexin 26 hemichannel due to an applied electric field; A molecular dynamics simulation study

Journal of molecular graphics & modelling, 2017-05, Vol.73, p.108-114

2017

Volltextzugriff (PDF)

The role of connexins in ear and skin physiology — Functional insights from disease-associated mutations

Biochimica et biophysica acta, 2013-01, Vol.1828 (1), p.167-178

2013

Volltextzugriff (PDF)

Connexin26 ( GJB2 ) deficiency reduces active cochlear amplification leading to late-onset hearing loss

Neuroscience, 2015-01, Vol.284, p.719-729

2015

Volltextzugriff (PDF)

Connexin 32 induces pro-tumorigenic features in MCF10A normal breast cells and MDA-MB-231 metastatic breast cancer cells

Biochimica et biophysica acta. Molecular cell research, 2020-12, Vol.1867 (12), p.118851-118851, Article 118851

2020

Volltextzugriff (PDF)

Deafness induced by Connexin 26 (GJB2) deficiency is not determined by endocochlear potential (EP) reduction but is associated with cochlear developmental disorders

Biochemical and biophysical research communications, 2014-05, Vol.448 (1), p.28-32

2014

Volltextzugriff (PDF)

Importance of Connexin-43 based gap junction in cirrhosis and acute-on-chronic liver failure

Journal of hepatology, 2013-06, Vol.58 (6), p.1194-1200

2013

Volltextzugriff (PDF)

Cryo-EM structure of an open conformation of a gap junction hemichannel in lipid bilayer nanodiscs

Structure (London), 2021-09, Vol.29 (9), p.1040-1047.e3

2021

Volltextzugriff (PDF)

Priming central sound processing circuits through induction of spontaneous activity in the cochlea before hearing onset

Trends in neurosciences (Regular ed.), 2024-07, Vol.47 (7), p.522-537

2024

Volltextzugriff (PDF)

Connexins in epidermal homeostasis and skin disease

Biochimica et biophysica acta, 2012-08, Vol.1818 (8), p.1952-1961

2012

Volltextzugriff (PDF)

More than keratitis, ichthyosis, and deafness: Multisystem effects of lethal GJB2 mutations

Journal of the American Academy of Dermatology, 2019-03, Vol.80 (3), p.617-625

2019

Volltextzugriff (PDF)

Investigation of the hearing levels of siblings affected by a single GJB2 variant: Possibility of genetic modifiers

International journal of pediatric otorhinolaryngology, 2021-10, Vol.149, p.110840-110840, Article 110840

2021

Volltextzugriff (PDF)

Genetic Factors Contribute to the Phenotypic Variability in GJB2-Related Hearing Impairment

The Journal of molecular diagnostics : JMD, 2023-11, Vol.25 (11), p.827-837

2023

Volltextzugriff (PDF)

Integrative analyses identified ion channel genes GJB2 and SCNN1B as prognostic biomarkers and therapeutic targets for lung adenocarcinoma

Lung cancer (Amsterdam, Netherlands), 2021-08, Vol.158, p.29-39

2021

Volltextzugriff (PDF)

Prevalence of the GJB2 mutations and the del(GJB6-D13S1830) mutation in Brazilian patients with deafness

Hearing research, 2004-10, Vol.196 (1), p.87-93

2004

Volltextzugriff (PDF)

Structural studies of N-terminal mutants of Connexin 26 and Connexin 32 using (1)H NMR spectroscopy

Archives of biochemistry and biophysics, 2016-10, Vol.608, p.8-19

2016

Volltextzugriff (PDF)

The role of Connexin26 regulated by MiR-2114-3p in the pathogenesis of ovarian cancer

Biochemical and biophysical research communications, 2023-01, Vol.640, p.105-116

2023

Volltextzugriff (PDF)

Spectrum and frequency of GJB2, GJB6 and SLC26A4 gene mutations among nonsyndromic hearing loss patients in eastern part of India

Gene, 2015-12, Vol.573 (2), p.239-245

2015

Volltextzugriff (PDF)

Epidemiology, etiology, genetic variants in non- syndromic hearing loss in Iran: A systematic review and meta‐analysis

International journal of pediatric otorhinolaryngology, 2023-05, Vol.168, p.111512-111512, Article 111512

2023

Volltextzugriff (PDF)

1 – 25 von 362

Suche als RSS-Feed

Aktive Filter

KollektionElsevier ScienceDirect Journals Complete

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(361)
Mit Volltextzugriff
(355)

Publikationsform

Artikel
(362)

Sprache

Erscheinungsjahr

n.n

Thema

Connexin 26
(340)
Science & Technology
(334)
Life Sciences & Biomedicine
(333)
Humans
(281)
Connexins - Genetics
(265)
Female
(156)
Male
(151)
Mutation
(147)
Otorhinolaryngology
(134)
Animals
(116)
Pediatrics
(103)
Deafness - Genetics
(93)
Gjb2
(80)
Child
(79)
Connexins - Metabolism
(79)
Hearing Loss, Sensorineural - Genetics
(78)
Otolaryngology
(78)
Biological And Medical Sciences
(76)
Child, Preschool
(66)
Adolescent
(61)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Cellular mechanisms of connexin-based inherited diseases

Tricellular adherens junctions provide a cell surface delivery platform for connexin 26/30 oligomers in the cochlea

Heart and liver connexin expression related to the first stage of aging: A study on naturally aged animals

Identification of homozygous mutations for hearing loss

Generation of hiPSC line UMi030-A from an individual with the hearing loss-related GJB2 mutation c.109G > A

Computational Studies of Molecular Permeation through Connexin26 Channels

The p.Gly130Val mutation in the GJB2 gene: A familiar case of autosomal dominant non-syndromic hearing loss

Deconstruction of the human connexin 26 hemichannel due to an applied electric field; A molecular dynamics simulation study

The role of connexins in ear and skin physiology — Functional insights from disease-associated mutations

Connexin26 ( GJB2 ) deficiency reduces active cochlear amplification leading to late-onset hearing loss

Connexin 32 induces pro-tumorigenic features in MCF10A normal breast cells and MDA-MB-231 metastatic breast cancer cells

Deafness induced by Connexin 26 (GJB2) deficiency is not determined by endocochlear potential (EP) reduction but is associated with cochlear developmental disorders

Importance of Connexin-43 based gap junction in cirrhosis and acute-on-chronic liver failure

Cryo-EM structure of an open conformation of a gap junction hemichannel in lipid bilayer nanodiscs

Priming central sound processing circuits through induction of spontaneous activity in the cochlea before hearing onset

Connexins in epidermal homeostasis and skin disease

More than keratitis, ichthyosis, and deafness: Multisystem effects of lethal GJB2 mutations

Investigation of the hearing levels of siblings affected by a single GJB2 variant: Possibility of genetic modifiers

Genetic Factors Contribute to the Phenotypic Variability in GJB2-Related Hearing Impairment

Integrative analyses identified ion channel genes GJB2 and SCNN1B as prognostic biomarkers and therapeutic targets for lung adenocarcinoma

Prevalence of the GJB2 mutations and the del(GJB6-D13S1830) mutation in Brazilian patients with deafness

Structural studies of N-terminal mutants of Connexin 26 and Connexin 32 using (1)H NMR spectroscopy

The role of Connexin26 regulated by MiR-2114-3p in the pathogenesis of ovarian cancer

Spectrum and frequency of GJB2, GJB6 and SLC26A4 gene mutations among nonsyndromic hearing loss patients in eastern part of India

Epidemiology, etiology, genetic variants in non- syndromic hearing loss in Iran: A systematic review and meta‐analysis

Aktive Filter

Suchergebnisse filtern