UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 320

Sortiert nach

The investigational drug ZEN-3694, a novel BET-bromodomain inhibitor, inhibits multiple tumor immune escape mechanisms and has the potential to combine with immunotherapies

European journal of cancer (1990), 2016-12, Vol.69, p.S88-S88

2016

Volltextzugriff (PDF)

560 ZEN3365 is a novel BET bromodomain inhibitor for the treatment of hematologic malignancies and solid tumors

European journal of cancer (1990), 2014-11, Vol.50, p.181-181

2014

Volltextzugriff (PDF)

Human Methionine Synthase: cDNA Cloning and Identification of Mutations in Patients of the cblG Complementation Group of Folate/Cobalamin Disorders

Human molecular genetics, 1996-12, Vol.5 (12), p.1867-1874

1996

Volltextzugriff (PDF)

RVX-208, an inducer of ApoA-I in humans, is a BET bromodomain antagonist

PloS one, 2013-12, Vol.8 (12), p.e83190

2013

Volltextzugriff (PDF)

Recognition of RNA Polymerase II and Transcription Bubbles by XPG, CSB, and TFIIH: Insights for Transcription-Coupled Repair and Cockayne Syndrome

Molecular cell, 2005-10, Vol.20 (2), p.187-198

2005

Volltextzugriff (PDF)

RNA interference in mammals: behind the screen

Briefings in functional genomics, 2011-07, Vol.10 (4), p.215-226

2011

Volltextzugriff (PDF)

Antibiofilm Activity of Manuka Honey in Combination with Antibiotics

International journal of bacteriology, 2014-01, Vol.2014, p.795281-7

2014

Volltextzugriff (PDF)

Abstract P3-06-07: The BET bromodomain inhibitors ZEN-3694 and ZEN-3309 targets several mechanisms of resistance to endocrine therapies in preclinical models of ER+ breast cancers

Cancer research (Chicago, Ill.), 2018-02, Vol.78 (4_Supplement), p.P3-P3-06-07

2018

Volltextzugriff (PDF)

Coding Sequence Mutations in the Alpha Subunit of Propionyl-CoA Carboxylase in Patients with Propionic Acidemia

Molecular genetics and metabolism, 1999-05, Vol.67 (1), p.11-22

1999

Volltextzugriff (PDF)

Functionally Null Mutations in Patients with the cblG-Variant Form of Methionine Synthase Deficiency

American journal of human genetics, 1998-08, Vol.63 (2), p.409-414

1998

Volltextzugriff (PDF)

Expression in Escherichia coli of N- and C-terminally deleted human holocarboxylase synthetase. Influence of the N-terminus on biotinylation and identification of a minimum functional protein

The Journal of biological chemistry, 2001-04, Vol.276 (15), p.12310-12316

2001

Volltextzugriff (PDF)

Structure of the PCCA Gene and Distribution of Mutations Causing Propionic Acidemia

Molecular genetics and metabolism, 2001-09, Vol.74 (1-2), p.238-247

2001

Volltextzugriff (PDF)

Overview of mutations in the PCCA and PCCB genes causing propionic acidemia

Human mutation, 1999-01, Vol.14 (4), p.275-282

1999

Volltextzugriff (PDF)

Mechanism of Biotin Responsiveness in Biotin-Responsive Multiple Carboxylase Deficiency

Molecular genetics and metabolism, 1999-02, Vol.66 (2), p.80-90

1999

Volltextzugriff (PDF)

Detection of a Normally Rare Transcript in Propionic Acidemia Patients with mRNA Destabilizing Mutations in the PCCA Gene

Human molecular genetics, 1999-01, Vol.8 (1), p.107-113

1999

Volltextzugriff (PDF)

Clustering of Mutations in the Biotin-Binding Region of Holocarboxylase Synthetase in Biotin-Responsive Multiple Carboxylase Deficiency

Human molecular genetics, 1996-07, Vol.5 (7), p.1011-1016

1996

Volltextzugriff (PDF)

Linkage analysis of the Nail-Patella syndrome

American journal of human genetics, 1995, Vol.56 (1), p.243-247

1995

Volltextzugriff (PDF)

Novel mutations and DNA-based screening in non-Jewish carriers of Tay-Sachs disease

American journal of human genetics, 1997-05, Vol.60 (5), p.1099-1106

1997

Volltextzugriff (PDF)

Overview of Mutations in the PCCA and PCCB Genes Causing Propionic Acidemia

Human mutation, 1999-01, Vol.14 (4), p.275-282

1999

Volltextzugriff (PDF)

Biosatellite post-flight experiment: some effects of forced electrolyte imbalance in Macaca nemestrina

Aerospace medicine, 1971-02, Vol.42 (2), p.177

1971

Volltextzugriff (PDF)

EEG discriminators of delayed matching to sample performance in Macaca nemestrina

Physiology & behavior, 1971-01, Vol.6 (4), p.413-418

1971

Volltextzugriff (PDF)

Linkage analysis of the nail-patella syndrome

American journal of human biology, 1995-01, Vol.56 (1), p.243-247

1995

Volltextzugriff (PDF)

The standardized radiography curriculum: apples, oranges, kumquats

Radiologic technology, 1988-05, Vol.59 (5), p.433

1988

Volltextzugriff (PDF)

WNT1 Mutations in Early-Onset Osteoporosis and Osteogenesis Imperfecta

The New England journal of medicine, 2013-05, Vol.368 (19), p.1809-1816

2013

Volltextzugriff (PDF)

Genomic DNA Methylation Signatures Enable Concurrent Diagnosis and Clinical Genetic Variant Classification in Neurodevelopmental Syndromes

American journal of human genetics, 2018-01, Vol.102 (1), p.156-174

2018

Volltextzugriff (PDF)

1 – 25 von 320

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(298)
Mit Volltextzugriff
(293)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(206)
Life Sciences & Biomedicine
(191)
Humans
(113)
Male
(100)
Animals
(92)
Female
(91)
Biological And Medical Sciences
(80)
Neurosciences & Neurology
(55)
Genetics & Heredity
(47)
Medical Sciences
(46)
Rats
(44)
Neurosciences
(43)
Fundamental And Applied Biological Sciences. Psychology
(37)
Rats, Sprague-Dawley
(35)
Adult
(33)
Endocrinology & Metabolism
(29)
Mutation
(29)
Middle Aged
(27)
Child
(24)
Corticosterone - Blood
(21)

15 weitere anzeigen...

Weniger anzeigen...

Kollektion

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

The investigational drug ZEN-3694, a novel BET-bromodomain inhibitor, inhibits multiple tumor immune escape mechanisms and has the potential to combine with immunotherapies

560 ZEN3365 is a novel BET bromodomain inhibitor for the treatment of hematologic malignancies and solid tumors

Human Methionine Synthase: cDNA Cloning and Identification of Mutations in Patients of the cblG Complementation Group of Folate/Cobalamin Disorders

RVX-208, an inducer of ApoA-I in humans, is a BET bromodomain antagonist

Recognition of RNA Polymerase II and Transcription Bubbles by XPG, CSB, and TFIIH: Insights for Transcription-Coupled Repair and Cockayne Syndrome

RNA interference in mammals: behind the screen

Antibiofilm Activity of Manuka Honey in Combination with Antibiotics

Abstract P3-06-07: The BET bromodomain inhibitors ZEN-3694 and ZEN-3309 targets several mechanisms of resistance to endocrine therapies in preclinical models of ER+ breast cancers

Coding Sequence Mutations in the Alpha Subunit of Propionyl-CoA Carboxylase in Patients with Propionic Acidemia

Functionally Null Mutations in Patients with the cblG-Variant Form of Methionine Synthase Deficiency

Expression in Escherichia coli of N- and C-terminally deleted human holocarboxylase synthetase. Influence of the N-terminus on biotinylation and identification of a minimum functional protein

Structure of the PCCA Gene and Distribution of Mutations Causing Propionic Acidemia

Overview of mutations in the PCCA and PCCB genes causing propionic acidemia

Mechanism of Biotin Responsiveness in Biotin-Responsive Multiple Carboxylase Deficiency

Detection of a Normally Rare Transcript in Propionic Acidemia Patients with mRNA Destabilizing Mutations in the PCCA Gene

Clustering of Mutations in the Biotin-Binding Region of Holocarboxylase Synthetase in Biotin-Responsive Multiple Carboxylase Deficiency

Linkage analysis of the Nail-Patella syndrome

Novel mutations and DNA-based screening in non-Jewish carriers of Tay-Sachs disease

Overview of Mutations in the PCCA and PCCB Genes Causing Propionic Acidemia

Biosatellite post-flight experiment: some effects of forced electrolyte imbalance in Macaca nemestrina

EEG discriminators of delayed matching to sample performance in Macaca nemestrina

Linkage analysis of the nail-patella syndrome

The standardized radiography curriculum: apples, oranges, kumquats

WNT1 Mutations in Early-Onset Osteoporosis and Osteogenesis Imperfecta

Genomic DNA Methylation Signatures Enable Concurrent Diagnosis and Clinical Genetic Variant Classification in Neurodevelopmental Syndromes

Suchergebnisse filtern