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...

Combined genetic approaches yield a 48% diagnostic rate in a large cohort of French hearing-impaired patients

Scientific reports, 2017-12, Vol.7 (1), p.16783-10, Article 16783

2017

Volltextzugriff (PDF)

Noninvasive prenatal diagnosis of genetic diseases induced by triplet repeat expansion by linked read haplotyping and Bayesian approach

Scientific reports, 2022-07, Vol.12 (1), p.11423-11423, Article 11423

2022

Volltextzugriff (PDF)

Audiological findings in 100 USH2 patients

Clinical genetics, 2012-11, Vol.82 (5), p.433-438

2012

Volltextzugriff (PDF)

Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90

Journal of medical genetics, 2006-09, Vol.43 (9), p.763-768

2006

Volltextzugriff (PDF)

Mutation of SLC9A1, encoding the major Na⁺/H⁺ exchanger, causes ataxia-deafness Lichtenstein-Knorr syndrome

Human molecular genetics, 2015-01, Vol.24 (2), p.463-470

2015

Volltextzugriff (PDF)

Ureteral sarcoma in a dog

Journal of small animal practice, 2007-12, Vol.48 (12), p.699-701

2007

Volltextzugriff (PDF)

The role of the tolerance-fecundity trade-off in maintaining intraspecific seed trait variation in a widespread dimorphic herb

Plant biology (Stuttgart, Germany), 2013-09, Vol.15 (5), p.899-909

2013

Volltextzugriff (PDF)

Assessment of a blood preservation protocol for use in ferrets before transfusion

Veterinary record, 2014-03, Vol.174 (11), p.277-277

2014

Volltextzugriff (PDF)

Identification of a gene from Xp21 with similarity to the tctex-1 gene of the murine t complex

Human molecular genetics, 1994-02, Vol.3 (2), p.257-263

1994

Volltextzugriff (PDF)

Loss of function of Ywhah in mice induces deafness and cochlear outer hair cells' degeneration

Cell death discovery, 2016-03, Vol.2 (1), p.16017-16017, Article 16017

2016

Volltextzugriff (PDF)

Intraoperative electrical stimulation in awake craniotomy: methodological aspects of current practice

Neurosurgical focus, 2010-02, Vol.28 (2), p.E7-E7

2010

Volltextzugriff (PDF)

Genomic sequencing reveals the structure of the Kcnk6 and map3k11 genes and their close vicinity to the sipa1 gene on mouse chromosome 19

Cytogenetic and genome research, 2000-01, Vol.89 (1-2), p.85-88

2000

Volltextzugriff (PDF)

PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome

The Journal of clinical investigation, 2010-06, Vol.120 (6), p.1812-1823

2010

Volltextzugriff (PDF)

High magnetic field amplification for improving the sensitivity of Hall sensors

IEEE sensors journal, 2006-06, Vol.6 (3), p.707-713

2006

Volltextzugriff (PDF)

A heat shock gene at 14q22: mapping and expression

Human molecular genetics, 1994-10, Vol.3 (10), p.1819-1822

1994

Volltextzugriff (PDF)

Physical and Transcription Map in the Region 14q24.3: Identification of Six Novel Transcripts

Genomics (San Diego, Calif.), 1997-07, Vol.43 (2), p.130-140

1997

Volltextzugriff (PDF)

Persistent Left Cranial Vena Cava Causing Oesophageal Obstruction and Consequent Megaoesophagus in a Dog

Journal of comparative pathology, 2006-08, Vol.135 (2-3), p.150-152

2006

Volltextzugriff (PDF)

SpαV/41 : a common spectrin polymorphism at the αIV-αV domain junction : relevance to the expression level of hereditary elliptocytosis due to α-spectrin variants located in trans

The Journal of clinical investigation, 1991-06, Vol.87 (6), p.2169-2177

1991

Volltextzugriff (PDF)

Molecular updates on Usher syndrome

Journal français d'ophtalmologie, 2005-01, Vol.28 (1), p.93-97

Roux, A-F

2005

Volltextzugriff (PDF)

Prevention by daily soluble aspirin of colorectal adenoma recurrence: 4-year results of the APACC randomised trial

Gut, 2012-02, Vol.61 (2), p.255-261

2012

Volltextzugriff (PDF)

Changes in anion permeability following hypotonic challenge in rat brain endothelial cells: different responses in primary cultures and in immortalised RBE4 cells

FEBS letters, 1997-11, Vol.417 (3), p.395-399

1997

Volltextzugriff (PDF)

Banques de données de mutations : enjeux et perspectives pour les maladies génétiques orphelines

Pathologie biologie (Paris), 2010-10, Vol.58 (5), p.387-395

2010

Volltextzugriff (PDF)

Genetic mutation databases: stakes and perspectives for orphan genetic diseases

Pathologie biologie (Paris), 2010-10, Vol.58 (5), p.387-395

2010

Volltextzugriff (PDF)

Spectrin Oran (αII/21), a new spectrin variant concerning the αII domain and causing severe elliptocytosis in the homozygous state

Blood, 1988-04, Vol.71 (4), p.1039-1047

1988

Volltextzugriff (PDF)

Cyclooxygenase-2 expression and recurrence of colorectal adenomas: effect of aspirin chemoprevention

Gut, 2010-05, Vol.59 (5), p.622-629

2010

Volltextzugriff (PDF)

1 – 25 von 5.743

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(4.653)
Mit Volltextzugriff
(4.477)

Publikationsform

6 weitere anzeigen...

Weniger anzeigen...

Sprache

5 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Science & Technology
(2.988)
Life Sciences & Biomedicine
(1.947)
Humans
(1.697)
Female
(1.093)
Male
(920)
Physical Sciences
(790)
Biological And Medical Sciences
(749)
Adult
(658)
Middle Aged
(632)
Life Sciences
(589)
Technology
(562)
Physics
(552)
Medical Sciences
(508)
Animals
(468)
Aged
(435)
Exact Sciences And Technology
(339)
Fundamental And Applied Biological Sciences. Psychology
(281)
Engineering
(280)
Adolescent
(273)
Chemistry
(212)

15 weitere anzeigen...

Weniger anzeigen...

Kollektion

IngentaConnect
(2.633)
MEDLINE
(2.165)
EZB Electronic Journals Library
(1.932)
Elsevier ScienceDirect Journals Complete
(1.868)
Journals@Ovid Full Text
(1.155)
Elsevier Journal Backfiles on ScienceDirect (DFG Nationallizenzen)
(890)
Publisher or Other Site
(753)
IngentaConnect Journals
(747)
Wiley-Blackwell Journals
(524)
Springer journals
(475)
Wiley Online Library
(390)
SpringerLINK Contemporary (Konsortium Baden-Württemberg)
(342)
Oxford Journals
(255)
IEEE Xplore
(240)
Oxford Journals 2020 Medicine
(172)
JSTOR
(154)
Taylor & Francis Journals Complete
(109)
Taylor & Francis Online
(109)
Taylor & Francis Journals Auto-Holdings Collection
(105)
Springer Nature - Connect here FIRST to enable access
(104)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(11)
... seit 90 Tagen
(29)

Menü

Weitere Dienste

Einstellungen

Combined genetic approaches yield a 48% diagnostic rate in a large cohort of French hearing-impaired patients

Noninvasive prenatal diagnosis of genetic diseases induced by triplet repeat expansion by linked read haplotyping and Bayesian approach

Audiological findings in 100 USH2 patients

Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90

Mutation of SLC9A1, encoding the major Na⁺/H⁺ exchanger, causes ataxia-deafness Lichtenstein-Knorr syndrome

Ureteral sarcoma in a dog

The role of the tolerance-fecundity trade-off in maintaining intraspecific seed trait variation in a widespread dimorphic herb

Assessment of a blood preservation protocol for use in ferrets before transfusion

Identification of a gene from Xp21 with similarity to the tctex-1 gene of the murine t complex

Loss of function of Ywhah in mice induces deafness and cochlear outer hair cells' degeneration

Intraoperative electrical stimulation in awake craniotomy: methodological aspects of current practice

Genomic sequencing reveals the structure of the Kcnk6 and map3k11 genes and their close vicinity to the sipa1 gene on mouse chromosome 19

PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome

High magnetic field amplification for improving the sensitivity of Hall sensors

A heat shock gene at 14q22: mapping and expression

Physical and Transcription Map in the Region 14q24.3: Identification of Six Novel Transcripts

Persistent Left Cranial Vena Cava Causing Oesophageal Obstruction and Consequent Megaoesophagus in a Dog

SpαV/41 : a common spectrin polymorphism at the αIV-αV domain junction : relevance to the expression level of hereditary elliptocytosis due to α-spectrin variants located in trans

Molecular updates on Usher syndrome

Prevention by daily soluble aspirin of colorectal adenoma recurrence: 4-year results of the APACC randomised trial

Changes in anion permeability following hypotonic challenge in rat brain endothelial cells: different responses in primary cultures and in immortalised RBE4 cells

Banques de données de mutations : enjeux et perspectives pour les maladies génétiques orphelines

Genetic mutation databases: stakes and perspectives for orphan genetic diseases

Spectrin Oran (αII/21), a new spectrin variant concerning the αII domain and causing severe elliptocytosis in the homozygous state

Cyclooxygenase-2 expression and recurrence of colorectal adenomas: effect of aspirin chemoprevention

Suchergebnisse filtern