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...

Fabrication of Necklace-like Structures via Electrospinning

Langmuir, 2010-01, Vol.26 (2), p.1186-1190

2010

Volltextzugriff (PDF)

Analysis of genotype–phenotype relationships in 90 Chinese probands with Waardenburg syndrome

Human genetics, 2022-04, Vol.141 (3-4), p.839-852

2022

Volltextzugriff (PDF)

Comprehensive genetic testing of Chinese SNHL patients and variants interpretation using ACMG guidelines and ethnically matched normal controls

European journal of human genetics : EJHG, 2020-02, Vol.28 (2), p.231-243

2020

Volltextzugriff (PDF)

Genomic and phenotypic landscapes of X-linked hereditary hearing loss in the Chinese population

Orphanet journal of rare diseases, 2024-09, Vol.19 (1), p.342-13, Article 342

2024

Volltextzugriff (PDF)

Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China

Journal of translational medicine, 2009-09, Vol.7 (1), p.79-79, Article 79

2009

Volltextzugriff (PDF)

Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, China

PloS one, 2015-08, Vol.10 (8), p.e0135088-e0135088

2015

Volltextzugriff (PDF)

Clinical and molecular findings in a Chinese family with a de novo mitochondrial A1555G mutation

BMC medical genomics, 2022-05, Vol.15 (1), p.121-121, Article 121

2022

Volltextzugriff (PDF)

Isolated human islets require hyperoxia to maintain islet mass, metabolism, and function

Biochemical and biophysical research communications, 2016-02, Vol.470 (3), p.534-538

2016

Volltextzugriff (PDF)

Genetic and phenotypic heterogeneity in Chinese patients with Waardenburg syndrome type II

PloS one, 2013-10, Vol.8 (10), p.e77149-e77149

2013

Volltextzugriff (PDF)

A subunit of V-ATPases, ATP6V1B2, underlies the pathology of intellectual disability

EBioMedicine, 2019-07, Vol.45, p.408-421

2019

Volltextzugriff (PDF)

Analysis of the genotype-phenotype correlation of MYO15A variants in Chinese non-syndromic hearing loss patients

BMC medical genomics, 2022-03, Vol.15 (1), p.71-71, Article 71

2022

Volltextzugriff (PDF)

Mitochondrial tRNASer(UCN) mutations associated non-syndromic sensorineural hearing loss in Chinese families

Heliyon, 2024-03, Vol.10 (6), p.e27041-e27041, Article e27041

2024

Volltextzugriff (PDF)

A Rapid Capillary-Pressure Driven Micro-Channel to Demonstrate Newtonian Fluid Behavior of Zebrafish Blood at High Shear Rates

Scientific reports, 2017-05, Vol.7 (1), p.1980-8, Article 1980

2017

Volltextzugriff (PDF)

Establishment of an iPSC line (CPGHi005-A) from a patient with Waardenburg syndrome carrying a heterozygous SVA-F retrotransposon insertion into SOX10

Stem cell research, 2022-07, Vol.62, p.102831-102831, Article 102831

2022

Volltextzugriff (PDF)

Characterization of SH3GLB1 in the auditory system and its potential role in mitophagy

Genes & diseases, 2024-07, Vol.11 (4), p.101018-101018, Article 101018

2024

Volltextzugriff (PDF)

Spatial Variations in Vitreous Oxygen Consumption

PloS one, 2016-03, Vol.11 (3), p.e0149961-e0149961

2016

Volltextzugriff (PDF)

KCNJ10 may not be a contributor to nonsyndromic enlargement of vestibular aqueduct (NSEVA) in Chinese subjects

PloS one, 2014-11, Vol.9 (11), p.e108134-e108134

2014

Volltextzugriff (PDF)

GJB2 mutation spectrum in 2063 Chinese patients with nonsyndromic hearing impairment

Journal of translational medicine, 2009-04, Vol.7 (26), p.26-26, Article 26

2009

Volltextzugriff (PDF)

A follow‐up study of a Chinese family with Waardenburg syndrome type II caused by a truncating mutation of MITF gene

Molecular genetics & genomic medicine, 2020-12, Vol.8 (12), p.e1520-n/a

2020

Volltextzugriff (PDF)

Extremely discrepant mutation spectrum of SLC26A4 between Chinese patients with isolated Mondini deformity and enlarged vestibular aqueduct

Journal of translational medicine, 2011-09, Vol.9 (1), p.167-167, Article 167

2011

Volltextzugriff (PDF)

Intervention study of tai chi training on the intestinal flora of college student basketball players

Medicine (Baltimore), 2023-09, Vol.102 (36), p.e35044

2023

Volltextzugriff (PDF)

SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss

Genetics in medicine, 2008-08, Vol.10 (8), p.586-592

2008

Volltextzugriff (PDF)

The prevalence of the 235delC GJB2 mutation in a Chinese deaf population

Genetics in medicine, 2007-05, Vol.9 (5), p.283-289

2007

Volltextzugriff (PDF)

Highly controllable and reliable ultra-thin Parylene deposition

Micro and nano systems letters, 2018-10, Vol.6 (1), p.1-7, Article 5

2018

Volltextzugriff (PDF)

Molecular etiology of hearing impairment in Inner Mongolia: mutations in SLC26A4 gene and relevant phenotype analysis

Journal of translational medicine, 2008-11, Vol.6 (1), p.74-74, Article 74

2008

Volltextzugriff (PDF)

1 – 25 von 184

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(151)
Mit Volltextzugriff
(157)

Publikationsform

Sprache

Englisch
(178)
Chinesisch
(6)

Erscheinungsjahr

n.n

Thema

Science & Technology
(128)
Life Sciences & Biomedicine
(55)
Technology
(53)
Physical Sciences
(45)
Humans
(43)
Engineering
(32)
Female
(32)
Mutation
(27)
Male
(26)
Hearing Loss
(25)
Science & Technology - Other Topics
(25)
Genetics & Heredity
(20)
Materials Science
(18)
Pedigree
(18)
Physics
(18)
China
(17)
Engineering, Electrical & Electronic
(17)
Materials Science, Multidisciplinary
(17)
Child
(16)
Nanoscience & Nanotechnology
(16)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

Fabrication of Necklace-like Structures via Electrospinning

Analysis of genotype–phenotype relationships in 90 Chinese probands with Waardenburg syndrome

Comprehensive genetic testing of Chinese SNHL patients and variants interpretation using ACMG guidelines and ethnically matched normal controls

Genomic and phenotypic landscapes of X-linked hereditary hearing loss in the Chinese population

Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China

Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, China

Clinical and molecular findings in a Chinese family with a de novo mitochondrial A1555G mutation

Isolated human islets require hyperoxia to maintain islet mass, metabolism, and function

Genetic and phenotypic heterogeneity in Chinese patients with Waardenburg syndrome type II

A subunit of V-ATPases, ATP6V1B2, underlies the pathology of intellectual disability

Analysis of the genotype-phenotype correlation of MYO15A variants in Chinese non-syndromic hearing loss patients

Mitochondrial tRNASer(UCN) mutations associated non-syndromic sensorineural hearing loss in Chinese families

A Rapid Capillary-Pressure Driven Micro-Channel to Demonstrate Newtonian Fluid Behavior of Zebrafish Blood at High Shear Rates

Establishment of an iPSC line (CPGHi005-A) from a patient with Waardenburg syndrome carrying a heterozygous SVA-F retrotransposon insertion into SOX10

Characterization of SH3GLB1 in the auditory system and its potential role in mitophagy

Spatial Variations in Vitreous Oxygen Consumption

KCNJ10 may not be a contributor to nonsyndromic enlargement of vestibular aqueduct (NSEVA) in Chinese subjects

GJB2 mutation spectrum in 2063 Chinese patients with nonsyndromic hearing impairment

A follow‐up study of a Chinese family with Waardenburg syndrome type II caused by a truncating mutation of MITF gene

Extremely discrepant mutation spectrum of SLC26A4 between Chinese patients with isolated Mondini deformity and enlarged vestibular aqueduct

Intervention study of tai chi training on the intestinal flora of college student basketball players

SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss

The prevalence of the 235delC GJB2 mutation in a Chinese deaf population

Highly controllable and reliable ultra-thin Parylene deposition

Molecular etiology of hearing impairment in Inner Mongolia: mutations in SLC26A4 gene and relevant phenotype analysis

Suchergebnisse filtern