UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 1.076

Sortiert nach

Nanoparticle-coated micro-optofluidic ring resonator as a detector for microscale gas chromatographic vapor analysis

Nanoscale, 2015-05, Vol.7 (2), p.9282-9289

2015

Volltextzugriff (PDF)

A novel locus for autosomal recessive nonsyndromic hearing impairment, DFNB63, maps to chromosome 11q13.2-q13.4

Journal of molecular medicine (Berlin, Germany), 2007-04, Vol.85 (4), p.397-404

2007

Volltextzugriff (PDF)

Clinical aspects of an autosomal dominantly inherited hearing impairment linked to the DFNA60 locus on chromosome 2q23.1–2q23.3

Hearing research, 2013-06, Vol.300, p.10-17

2013

Volltextzugriff (PDF)

Homozygosity mapping identifies genetic defects in four consanguineous families with retinal dystrophy from Pakistan

Clinical genetics, 2013-09, Vol.84 (3), p.290-293

2013

Volltextzugriff (PDF)

Flat Threshold and Mid-Frequency Hearing Impairment in a Dutch DFNA8/12 Family with a Novel Mutation in TECTA : Some Evidence for Protection of the Inner Ear

Audiology & neurotology, 2009, Vol.14 (3), p.153-162

2009

Volltextzugriff (PDF)

Flat Threshold and Mid-Frequency Hearing Impairment in a Dutch DFNA8/12 Family with a Novel Mutation in TECTA

Audiology & neurotology, 2009-03, Vol.14 (3), p.153-162

2009

Volltextzugriff (PDF)

A Nonsense Mutation in PDE6H Causes Autosomal-Recessive Incomplete Achromatopsia

American journal of human genetics, 2012-09, Vol.91 (3), p.527-532

2012

Volltextzugriff (PDF)

Glucose Control and Vascular Complications in Veterans with Type 2 Diabetes

The New England journal of medicine, 2009-01, Vol.360 (2), p.129-139

2009

Volltextzugriff (PDF)

Genomic approaches for the discovery of genes mutated in inherited retinal degeneration

Cold Spring Harbor perspectives in medicine, 2014-08, Vol.4 (8), p.a017137-a017137

2014

Volltextzugriff (PDF)

μGC × μGC microsystem with resistive and optical detection

2015 Transducers - 2015 18th International Conference on Solid-State Sensors, Actuators and Microsystems (TRANSDUCERS), 2015, p.949-952

2015

Volltextzugriff (PDF)

ENVIRONMENTAL JUSTICE IN OREGON: IT'S THE LAW

Environmental law (Portland, Ore.), 2008-03, Vol.38 (2), p.413-455

Collin, Robert W.

2008

Volltextzugriff (PDF)

Environmental Racism: A Challenge to Community Development

Journal of black studies, 1995-01, Vol.25 (3), p.354-376

1995

Volltextzugriff (PDF)

OR11-002 - Mutations in MVK cause non-syndromic RP

Pediatric rheumatology online journal, 2013-11, Vol.11 (S1), p.A191-A191, Article A191

2013

Volltextzugriff (PDF)

Calibration-Free Multichannel Ellipsometry for Retardance Measurement

Journal of the Korean Physical Society, 2005-02, p.142-145

2005

Volltextzugriff (PDF)

Identification and expression of the first nonmammalian amyloid‐β precursor‐like protein APLP2 in the amphibian Xenopus laevis

European journal of biochemistry, 2004-05, Vol.271 (10), p.1906-1912

2004

Volltextzugriff (PDF)

Calibration-Free Multichannel Ellipsometry for Retardance Measurement

Journal of the Korean Physical Society, 2005, 46(2), , pp.142-145

2005

Volltextzugriff (PDF)

Randomized Evaluation of the Effects of Anacetrapib through Lipid-modification (REVEAL) – A large-scale, randomized, placebo-controlled trial of the clinical effects of anacetrapib among people with established vascular disease: trial design, recruitment and baseline characteristics

The American heart journal, 2017-05, Vol.187, p.182-190

Landray, Martin J

2017

Volltextzugriff (PDF)

Alfentanil supplemented anaesthesia for short procedures. A double-blind study of alfentanil used with etomidate and enflurane for day cases

Anaesthesia, 1986-05, Vol.41 (5), p.477-481

1986

Volltextzugriff (PDF)

Toward a new theory of nonprofit liability

Administration in social work, 1987-04, Vol.11 (Spring 87), p.15-24

Collin, R W

1987

Volltextzugriff (PDF)

Homozygosity mapping identifies genetic defects in four consanguineous families with retinal dystrophy from Pakistan

Clinical genetics, 2013, Vol.84 (3), p.290-293

2013

Volltextzugriff (PDF)

Homelessness: The Policy and the Law

The Urban lawyer, 1984-01, Vol.16 (2), p.317-329

Collin, Robert W.

1984

Volltextzugriff (PDF)

Alfentanil supplemented anaesthesia for short procedures

Anaesthesia, 1986-05, Vol.41 (5), p.477-481

1986

Volltextzugriff (PDF)

Blood-brain barrier breakdown in the aging human hippocampus

Neuron (Cambridge, Mass.), 2015-01, Vol.85 (2), p.296-302

2015

Volltextzugriff (PDF)

Toward a New Theory of Nonprofit Liability

Administration in social work, 1987-05, Vol.11 (1), p.15-24

Collin, Robert W.

1987

Volltextzugriff (PDF)

Delivery of oligonucleotide‐based therapeutics: challenges and opportunities

EMBO molecular medicine, 2021-04, Vol.13 (4), p.e13243-n/a

2021

Volltextzugriff (PDF)

1 – 25 von 1.076

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(920)
Mit Volltextzugriff
(887)

Publikationsform

4 weitere anzeigen...

Weniger anzeigen...

Sprache

3 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 7 Tagen
(1)
... seit 90 Tagen
(5)

Menü

Weitere Dienste

Einstellungen

Nanoparticle-coated micro-optofluidic ring resonator as a detector for microscale gas chromatographic vapor analysis

A novel locus for autosomal recessive nonsyndromic hearing impairment, DFNB63, maps to chromosome 11q13.2-q13.4

Clinical aspects of an autosomal dominantly inherited hearing impairment linked to the DFNA60 locus on chromosome 2q23.1–2q23.3

Homozygosity mapping identifies genetic defects in four consanguineous families with retinal dystrophy from Pakistan

Flat Threshold and Mid-Frequency Hearing Impairment in a Dutch DFNA8/12 Family with a Novel Mutation in TECTA : Some Evidence for Protection of the Inner Ear

Flat Threshold and Mid-Frequency Hearing Impairment in a Dutch DFNA8/12 Family with a Novel Mutation in TECTA

A Nonsense Mutation in PDE6H Causes Autosomal-Recessive Incomplete Achromatopsia

Glucose Control and Vascular Complications in Veterans with Type 2 Diabetes

Genomic approaches for the discovery of genes mutated in inherited retinal degeneration

μGC × μGC microsystem with resistive and optical detection

ENVIRONMENTAL JUSTICE IN OREGON: IT'S THE LAW

Environmental Racism: A Challenge to Community Development

OR11-002 - Mutations in MVK cause non-syndromic RP

Calibration-Free Multichannel Ellipsometry for Retardance Measurement

Identification and expression of the first nonmammalian amyloid‐β precursor‐like protein APLP2 in the amphibian Xenopus laevis

Calibration-Free Multichannel Ellipsometry for Retardance Measurement

Randomized Evaluation of the Effects of Anacetrapib through Lipid-modification (REVEAL) – A large-scale, randomized, placebo-controlled trial of the clinical effects of anacetrapib among people with established vascular disease: trial design, recruitment and baseline characteristics

Alfentanil supplemented anaesthesia for short procedures. A double-blind study of alfentanil used with etomidate and enflurane for day cases

Toward a new theory of nonprofit liability

Homozygosity mapping identifies genetic defects in four consanguineous families with retinal dystrophy from Pakistan

Homelessness: The Policy and the Law

Alfentanil supplemented anaesthesia for short procedures

Blood-brain barrier breakdown in the aging human hippocampus

Toward a New Theory of Nonprofit Liability

Delivery of oligonucleotide‐based therapeutics: challenges and opportunities

Suchergebnisse filtern