UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 143

Sortiert nach

A home monitoring program including real-time wireless home spirometry in idiopathic pulmonary fibrosis: a pilot study on experiences and barriers

Respiratory research, 2018-05, Vol.19 (1), p.105-105, Article 105

2018

Volltextzugriff (PDF)

Associations with tight junction genes PARD3 and MAGI2 in Dutch patients point to a common barrier defect for coeliac disease and ulcerative colitis

Gut, 2008-04, Vol.57 (4), p.463-467

2008

Volltextzugriff (PDF)

A microarray screen for novel candidate genes in coeliac disease pathogenesis

Gut, 2004-07, Vol.53 (7), p.944-951

2004

Volltextzugriff (PDF)

Adaptation and validation of the Cambridge Pulmonary Hypertension Outcome Review (CAMPHOR) for the Netherlands

Netherlands heart journal, 2016-06, Vol.24 (6), p.417-424

2016

Volltextzugriff (PDF)

Correction to: Adaptation and validation of the Cambridge Pulmonary Hypertension Outcome Review (CAMPHOR) for the Netherlands

Netherlands heart journal, 2018-11, Vol.26 (11), p.579-579

2018

Volltextzugriff (PDF)

Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications

American journal of human genetics, 1989-12, Vol.45 (6), p.835-847

1989

Volltextzugriff (PDF)

The longitudinal use of EmPHasis-10 and CAMPHOR questionnaire health-related quality of life scores in patients with pulmonary arterial hypertension and chronic thromboembolic pulmonary hypertension

European heart journal, 2021-10, Vol.42 (Supplement_1)

2021

Volltextzugriff (PDF)

Association Analysis of MYO9B Gene Polymorphisms with Celiac Disease in a Swedish/Norwegian Cohort

Human Immunology, 2006-04, Vol.67 (4), p.341-345

2006

Volltextzugriff (PDF)

The interferon gamma gene in celiac disease: augmented expression correlates with tissue damage but no evidence for genetic susceptibility

Journal of autoimmunity, 2004-09, Vol.23 (2), p.183-190

2004

Volltextzugriff (PDF)

Characterization of Cxorf5 (71-7A), a novel human cDNA mapping to Xp22 and encoding a protein containing coiled-coil α-helical domains

Genomics (San Diego, Calif.), 1998-07, Vol.51 (2), p.243-250

1998

Volltextzugriff (PDF)

A gene from the Xp22.3 region shares homology with voltage-gated chloride channels

Human molecular genetics, 1994-04, Vol.3 (4), p.547-552

1994

Volltextzugriff (PDF)

C43 IF YOU'VE GOT TROUBLE: CHRONIC COUGH: Cough Measurements In Patients With Idiopathic Pulmonary Fibrosis (ipf)

American journal of respiratory and critical care medicine, 2015-01, Vol.191, p.1

2015

Volltextzugriff (PDF)

A103 IPF: MORE ABOUT THERAPY AND OUTCOMES: Effect Of Pirfenidone On Cough In Patients With Idiopathic Pulmonary Fibrosis

American journal of respiratory and critical care medicine, 2016-01, Vol.193, p.1

2016

Volltextzugriff (PDF)

Translation and validation of the King’s Brief Interstitial Lung Disease (K-BILD) questionnaire in French, Italian, Swedish, and Dutch

Chronic respiratory disease, 2017-05, Vol.14 (2), p.140-150

2017

Volltextzugriff (PDF)

A Novel Splicing Mutation in KCNQ2 in a Multigenerational Family with BFNC Followed for 25 Years

Epilepsia (Copenhagen), 2006-05, Vol.47 (5), p.851-859

2006

Volltextzugriff (PDF)

Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect

Nature genetics, 2005-12, Vol.37 (12), p.1341-1344

2005

Volltextzugriff (PDF)

C39 IPF: MORE ON DIAGNOSIS AND THERAPY: Quantitative Image Analysis Of Spirometry-Guided Hrct In A Phase 2 Study Of Prm-151 In Patients With Idiopathic Pulmonary Fibrosis

American journal of respiratory and critical care medicine, 2016-01, Vol.193, p.1

2016

Volltextzugriff (PDF)

Validation of the King's Sarcoidosis Questionnaire (KSQ) in a Dutch sarcoidosis population

Sarcoidosis, vasculitis, and diffuse lung diseases, 2016-03, Vol.33 (1), p.75-82

2016

Volltextzugriff (PDF)

B104 TICKET TO RIDE: MOVING FORWARD WITH SARCOIDOSIS EVALUATION AND TREATMENT: Steroid Treatment Optimization In Pulmonary Sarcoidosis

American journal of respiratory and critical care medicine, 2015-01, Vol.191, p.1

2015

Volltextzugriff (PDF)

Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy

Human genetics, 1985-01, Vol.70 (2), p.148-156

1985

Volltextzugriff (PDF)

Exon trapping. Application of a large-insert multiple-exon-trapping system

Methods in molecular biology (Clifton, N.J.), 2001, Vol.175, p.201

2001

Volltextzugriff (PDF)

The genes for X-linked ocular albinism (OA1) and microphthalmia with linear skin defects (MLS): cloning and characterization of the critical regions

Human molecular genetics, 1993-07, Vol.2 (7), p.947-952

1993

Volltextzugriff (PDF)

German Validation of the "King's Brief Interstitial Lung Disease (K-Bild) Health Status Questionnaire"

Pneumologie (Stuttgart, Germany), 2016-11, Vol.70 (11), p.742

2016

Volltextzugriff (PDF)

A high resolution deletion map of human chromosome Xp22

Nature genetics, 1993-07, Vol.4 (3), p.272-279

1993

Volltextzugriff (PDF)

Generation and fluorescent in situ hybridization mapping of yeast artificial chromosomes of 1p, 17p, 17q, and 19q from a hybrid cell line by high-density screening of an amplified library

Genomics (San Diego, Calif.), 1991-12, Vol.11 (4), p.1079-1087

1991

Volltextzugriff (PDF)

1 – 25 von 143

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(131)
Mit Volltextzugriff
(130)

Publikationsform

Artikel
(142)
Tagungsberichte
(1)

Sprache

1 weiteren anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Science & Technology
(88)
Life Sciences & Biomedicine
(77)
Humans
(62)
Female
(43)
Biological And Medical Sciences
(41)
Male
(34)
Animals
(28)
Medical Sciences
(24)
Genetics & Heredity
(23)
Fundamental And Applied Biological Sciences. Psychology
(21)
X Chromosome
(20)
Chromosome Mapping
(16)
Cattle
(15)
Veterinary Sciences
(14)
Genetics Of Eukaryotes. Biological And Molecular Evolution
(12)
Biochemistry & Molecular Biology
(11)
Celiac Disease - Genetics
(11)
Chromosome Deletion
(11)
Molecular Sequence Data
(11)
Muscular Dystrophies - Genetics
(11)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

A home monitoring program including real-time wireless home spirometry in idiopathic pulmonary fibrosis: a pilot study on experiences and barriers

Associations with tight junction genes PARD3 and MAGI2 in Dutch patients point to a common barrier defect for coeliac disease and ulcerative colitis

A microarray screen for novel candidate genes in coeliac disease pathogenesis

Adaptation and validation of the Cambridge Pulmonary Hypertension Outcome Review (CAMPHOR) for the Netherlands

Correction to: Adaptation and validation of the Cambridge Pulmonary Hypertension Outcome Review (CAMPHOR) for the Netherlands

Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications

The longitudinal use of EmPHasis-10 and CAMPHOR questionnaire health-related quality of life scores in patients with pulmonary arterial hypertension and chronic thromboembolic pulmonary hypertension

Association Analysis of MYO9B Gene Polymorphisms with Celiac Disease in a Swedish/Norwegian Cohort

The interferon gamma gene in celiac disease: augmented expression correlates with tissue damage but no evidence for genetic susceptibility

Characterization of Cxorf5 (71-7A), a novel human cDNA mapping to Xp22 and encoding a protein containing coiled-coil α-helical domains

A gene from the Xp22.3 region shares homology with voltage-gated chloride channels

C43 IF YOU'VE GOT TROUBLE: CHRONIC COUGH: Cough Measurements In Patients With Idiopathic Pulmonary Fibrosis (ipf)

A103 IPF: MORE ABOUT THERAPY AND OUTCOMES: Effect Of Pirfenidone On Cough In Patients With Idiopathic Pulmonary Fibrosis

Translation and validation of the King’s Brief Interstitial Lung Disease (K-BILD) questionnaire in French, Italian, Swedish, and Dutch

A Novel Splicing Mutation in KCNQ2 in a Multigenerational Family with BFNC Followed for 25 Years

Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect

C39 IPF: MORE ON DIAGNOSIS AND THERAPY: Quantitative Image Analysis Of Spirometry-Guided Hrct In A Phase 2 Study Of Prm-151 In Patients With Idiopathic Pulmonary Fibrosis

Validation of the King's Sarcoidosis Questionnaire (KSQ) in a Dutch sarcoidosis population

B104 TICKET TO RIDE: MOVING FORWARD WITH SARCOIDOSIS EVALUATION AND TREATMENT: Steroid Treatment Optimization In Pulmonary Sarcoidosis

Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy

Exon trapping. Application of a large-insert multiple-exon-trapping system

The genes for X-linked ocular albinism (OA1) and microphthalmia with linear skin defects (MLS): cloning and characterization of the critical regions

German Validation of the "King's Brief Interstitial Lung Disease (K-Bild) Health Status Questionnaire"

A high resolution deletion map of human chromosome Xp22

Generation and fluorescent in situ hybridization mapping of yeast artificial chromosomes of 1p, 17p, 17q, and 19q from a hybrid cell line by high-density screening of an amplified library

Suchergebnisse filtern