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...

Anthropoid primate-specific retroviral element THE1B controls expression of CRH in placenta and alters gestation length

PLoS biology, 2018-09, Vol.16 (9), p.e2006337-e2006337

2018

Volltextzugriff (PDF)

Distinct regional and subcellular localization of adenylyl cyclases type 1 and 8 in mouse brain

Neuroscience, 2007-05, Vol.146 (2), p.713-729

2007

Volltextzugriff (PDF)

Temporal and regional regulation of gene expression by calcium-stimulated adenylyl cyclase activity during fear memory

PloS one, 2010-10, Vol.5 (10), p.e13385-e13385

2010

Volltextzugriff (PDF)

The role of glucocorticoid receptor-dependent activity in the amygdala central nucleus and reversibility of early-life stress programmed behavior

Translational psychiatry, 2015-04, Vol.5 (4), p.e542-e542

2015

Volltextzugriff (PDF)

Impaired Synaptic Plasticity and cAMP Response Element-Binding Protein Activation in Ca2+/Calmodulin-Dependent Protein Kinase Type IV/Gr-Deficient Mice

The Journal of neuroscience, 2000-09, Vol.20 (17), p.6459-6472

2000

Volltextzugriff (PDF)

Genetic Approaches to Hypothalamic-Pituitary-Adrenal Axis Regulation

Neuropsychopharmacology (New York, N.Y.), 2016-01, Vol.41 (1), p.245-260

2016

Volltextzugriff (PDF)

The natural history of spinal neurofibromatosis: a critical review of clinical and genetic features

Clinical genetics, 2015-05, Vol.87 (5), p.401-410

2015

Volltextzugriff (PDF)

A 71‐nucleotide deletion in the periaxin gene in an Italian patient with late‐onset slowly progressive demyelinating Charcot‐Marie‐Tooth disease

European journal of neurology, 2020-10, Vol.27 (10), p.2109-2110

2020

Volltextzugriff (PDF)

Observations of Shelf‐Ocean Exchange in the Northern South Atlantic Bight Driven by the Gulf Stream

Journal of geophysical research. Oceans, 2023-07, Vol.128 (7), p.n/a

2023

Volltextzugriff (PDF)

T-cell glucocorticoid receptor is required to suppress COX-2-mediated lethal immune activation

Nature medicine, 2003-10, Vol.9 (10), p.1318-1322

2003

Volltextzugriff (PDF)

Generation of myometrium-specific Bmal1 knockout mice for parturition analysis

Reproduction fertility and development, 2012, Vol.24 (5), p.759

2012

Volltextzugriff (PDF)

Childhood neurofibromatosis type 2 (NF2) and related disorders: from bench to bedside and biologically targeted therapies

Acta otorhino-laryngologica italica, 2016-10, Vol.36 (5), p.345-367

2016

Volltextzugriff (PDF)

Altered Stress-Induced Anxiety in Adenylyl Cyclase Type VIII-Deficient Mice

The Journal of neuroscience, 2000-07, Vol.20 (13), p.4809-4820

2000

Volltextzugriff (PDF)

Kinesins in neurological inherited diseases: a novel motor-domain mutation in KIF5A gene in a patient from Southern Italy affected by hereditary spastic paraplegia

Acta neurologica Belgica, 2018-12, Vol.118 (4), p.643-646

2018

Volltextzugriff (PDF)

Exome sequencing reveals two FA2H mutations in a family with a complicated form of Hereditary Spastic Paraplegia and psychiatric impairments

Journal of the neurological sciences, 2017-01, Vol.372, p.347-349

2017

Volltextzugriff (PDF)

Further evidence that DDHD2 gene mutations cause autosomal recessive hereditary spastic paraplegia with thin corpus callosum

European journal of neurology, 2014-03, Vol.21 (3), p.e25-e26

2014

Volltextzugriff (PDF)

Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation

Neurology, 2010-06, Vol.74 (23), p.1919-1921

2010

Volltextzugriff (PDF)

A novel KIF5A mutation in an Italian family marked by spastic paraparesis and congenital deafness

Journal of the neurological sciences, 2014-08, Vol.343 (1), p.218-220

2014

Volltextzugriff (PDF)

A low-order wake interaction modeling framework for the performance of ocean current turbines under turbulent conditions

Renewable energy, 2022-11, Vol.200, p.1602-1617

2022

Volltextzugriff (PDF)

TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis

Journal of neurology, neurosurgery and psychiatry, 2011-05, Vol.82 (5), p.587-588

2011

Volltextzugriff (PDF)

Brain-derived neurotrophic factor and risk for primary adult-onset cranial-cervical dystonia

European journal of neurology, 2009-08, Vol.16 (8), p.949-952

2009

Volltextzugriff (PDF)

Coordinate Regulation of Prostaglandin Metabolism for Induction of Parturition in Mice

Endocrinology (Philadelphia), 2002-07, Vol.143 (7), p.2593-2598

2002

Volltextzugriff (PDF)

Charcot-Marie-Tooth type X: unusual phenotype of a novel CX32 mutation

European journal of neurology, 2008-10, Vol.15 (10), p.1140-1142

2008

Volltextzugriff (PDF)

CADASIL: Extended polymorphisms and mutational analysis of the NOTCH3 gene

Journal of neuroscience research, 2009-04, Vol.87 (5), p.1162-1167

2009

Volltextzugriff (PDF)

First mutation in the nuclear localization signal sequence of spastin protein identified in a patient with hereditary spastic paraplegia

European journal of neurology, 2013-01, Vol.20 (1), p.e22-e23

2013

Volltextzugriff (PDF)

1 – 25 von 539

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(493)
Mit Volltextzugriff
(447)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

1 weiteren anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Anthropoid primate-specific retroviral element THE1B controls expression of CRH in placenta and alters gestation length

Distinct regional and subcellular localization of adenylyl cyclases type 1 and 8 in mouse brain

Temporal and regional regulation of gene expression by calcium-stimulated adenylyl cyclase activity during fear memory

The role of glucocorticoid receptor-dependent activity in the amygdala central nucleus and reversibility of early-life stress programmed behavior

Impaired Synaptic Plasticity and cAMP Response Element-Binding Protein Activation in Ca2+/Calmodulin-Dependent Protein Kinase Type IV/Gr-Deficient Mice

Genetic Approaches to Hypothalamic-Pituitary-Adrenal Axis Regulation

The natural history of spinal neurofibromatosis: a critical review of clinical and genetic features

A 71‐nucleotide deletion in the periaxin gene in an Italian patient with late‐onset slowly progressive demyelinating Charcot‐Marie‐Tooth disease

Observations of Shelf‐Ocean Exchange in the Northern South Atlantic Bight Driven by the Gulf Stream

T-cell glucocorticoid receptor is required to suppress COX-2-mediated lethal immune activation

Generation of myometrium-specific Bmal1 knockout mice for parturition analysis

Childhood neurofibromatosis type 2 (NF2) and related disorders: from bench to bedside and biologically targeted therapies

Altered Stress-Induced Anxiety in Adenylyl Cyclase Type VIII-Deficient Mice

Kinesins in neurological inherited diseases: a novel motor-domain mutation in KIF5A gene in a patient from Southern Italy affected by hereditary spastic paraplegia

Exome sequencing reveals two FA2H mutations in a family with a complicated form of Hereditary Spastic Paraplegia and psychiatric impairments

Further evidence that DDHD2 gene mutations cause autosomal recessive hereditary spastic paraplegia with thin corpus callosum

Severe CMT type 2 with fatal encephalopathy associated with a novel MFN2 splicing mutation

A novel KIF5A mutation in an Italian family marked by spastic paraparesis and congenital deafness

A low-order wake interaction modeling framework for the performance of ocean current turbines under turbulent conditions

TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis

Brain-derived neurotrophic factor and risk for primary adult-onset cranial-cervical dystonia

Coordinate Regulation of Prostaglandin Metabolism for Induction of Parturition in Mice

Charcot-Marie-Tooth type X: unusual phenotype of a novel CX32 mutation

CADASIL: Extended polymorphisms and mutational analysis of the NOTCH3 gene

First mutation in the nuclear localization signal sequence of spastin protein identified in a patient with hereditary spastic paraplegia

Suchergebnisse filtern