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...

Mutations in Eml1 lead to ectopic progenitors and neuronal heterotopia in mouse and human

Nature neuroscience, 2014-07, Vol.17 (7), p.923-933

2014

Volltextzugriff (PDF)

Branching and nucleokinesis defects in migrating interneurons derived from doublecortin knockout mice

Human molecular genetics, 2006-05, Vol.15 (9), p.1387-1400

2006

Volltextzugriff (PDF)

Mutations in the β-tubulin gene TUBB2B result in asymmetrical polymicrogyria

Nature genetics, 2009-06, Vol.41 (6), p.746-752

2009

Volltextzugriff (PDF)

Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypes

PLoS genetics, 2013-01, Vol.9 (1), p.e1003094-e1003094

2013

Volltextzugriff (PDF)

Magnetic resonance imaging and histological studies of corpus callosal and hippocampal abnormalities linked to doublecortin deficiency

Journal of comparative neurology (1911), 2007-01, Vol.500 (2), p.239-254

2007

Volltextzugriff (PDF)

Novel Target Sequences for Pax-6 in the Brain-specific Activating Regions of the Rat Aldolase C Gene

The Journal of biological chemistry, 2002-12, Vol.277 (49), p.47190-47196

2002

Volltextzugriff (PDF)

Alternative Transcripts of Dclk1 and Dclk2 and Their Expression in Doublecortin Knockout Mice

Developmental neuroscience, 2008, Vol.30 (1-3), p.171-186

2008

Volltextzugriff (PDF)

Mutations in the [beta]-tubulin gene TUBB2B result in asymmetrical polymicrogyria

Nature genetics, 2009-06, Vol.41 (6), p.746-752

2009

Volltextzugriff (PDF)

Human disorders of cortical development: from past to present

The European journal of neuroscience, 2006-02, Vol.23 (4), p.877-893

2006

Volltextzugriff (PDF)

Mutations du gène EML1/Eml1 , progéniteurs neuronaux et hétérotopies chez l’homme et la souris

M.S. Médecine sciences, 2014-12, Vol.30 (12), p.1087-1090

2014

Volltextzugriff (PDF)

Correction: Mutation of the Diamond-Blackfan Anemia Gene Rps7 in Mouse Results in Morphological and Neuroanatomical Phenotypes

PLoS genetics, 2015-11, Vol.11 (11), p.e1005682-e1005682

2015

Volltextzugriff (PDF)

Branching and nucleokinesis defects in migrating interneurons derived from doublecortin knockout mice

Human molecular genetics, 2006-07, Vol.15 (13), p.2183-2183

2006

Volltextzugriff (PDF)

REVIEW ARTICLE: Human disorders of cortical development: from past to present

The European journal of neuroscience, 2006-02, Vol.23 (4), p.877-893

2006

Volltextzugriff (PDF)

Mutations in Eml1/EML1 lead to ectopic progenitors and neuronal heterotopia in mouse and human

M.S. Médecine sciences, 2014-12, Vol.30 (12), p.1087

2014

Volltextzugriff (PDF)

Metabolism of proline in a human leukemic lymphoblastoid cell line

Cancer research (Chicago, Ill.), 1978-11, Vol.38 (11 Pt 1), p.3950-3953

1978

Volltextzugriff (PDF)

Bidirectional activity and orientation-dependent specificity of the rat aldolase C promoter in transgenic mice

FEBS letters, 2001-06, Vol.499 (1), p.143-146

2001

Volltextzugriff (PDF)

High tyrosine kinase activity in normal nonproliferating cells

Nature (London), 1983-09, Vol.305 (5933), p.435-438

1983

Volltextzugriff (PDF)

DEFICIT OF SUPPRESSOR T CELLS IN ACTIVE MULTIPLE SCLEROSIS

The Lancet (British edition), 1980, Vol.316 (8206), p.1221-1223

1980

Volltextzugriff (PDF)

Upstream elements involved in vivo in activation of the brain-specific rat aldolase C gene. Role of binding sites for POU and winged helix proteins

The Journal of biological chemistry, 1998-11, Vol.273 (48), p.31806-31814

1998

Volltextzugriff (PDF)

Functional dissection of the brain-specific rat aldolase C gene promoter in transgenic mice. Essential role of two GC-rich boxes and an HNF3 binding site

The Journal of biological chemistry, 1995-09, Vol.270 (35), p.20316-20321

1995

Volltextzugriff (PDF)

CC Ar GG boxes, cis-acting elements with a dual specificity. Muscle-specific transcriptional activation and serum responsiveness

Journal of molecular biology, 1990-06, Vol.213 (4), p.677-686

1990

Volltextzugriff (PDF)

Functional Dissection of the Brain-specific Rat Aldolase C Gene Promoter in Transgenic Mice

The Journal of biological chemistry, 1995-09, Vol.270 (35), p.20316-20321

1995

Volltextzugriff (PDF)

Muscle-Specific Transcriptional Activation by CArG Box Requires Either Homophilic or Heterophilic Interactions of the CArG Box Binding Factors

Biochemical and biophysical research communications, 1993-08, Vol.195 (1), p.400-408

1993

Volltextzugriff (PDF)

Activation of Gene Expression via CArG Boxes during Myogenic Differentiation

Experimental cell research, 1993-03, Vol.205 (1), p.32-38

1993

Volltextzugriff (PDF)

1 – 25 von 36

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(36)
Mit Volltextzugriff
(31)

Publikationsform

Artikel
(36)

Sprache

Englisch
(34)
Französisch
(2)

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(21)
Science & Technology
(21)
Animals
(18)
Humans
(18)
Mice
(13)
Biochemistry & Molecular Biology
(11)
Biological And Medical Sciences
(9)
Fundamental And Applied Biological Sciences. Psychology
(9)
Life Sciences
(9)
Base Sequence
(8)
Molecular Sequence Data
(8)
Mutation
(8)
Molecular And Cellular Biology
(7)
Rats
(6)
Actins - Genetics
(5)
Binding Sites
(5)
Biochemistry, Molecular Biology
(5)
Gene Expression
(5)
Genetics & Heredity
(5)
Microtubule-Associated Proteins - Genetics
(5)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Mutations in Eml1 lead to ectopic progenitors and neuronal heterotopia in mouse and human

Branching and nucleokinesis defects in migrating interneurons derived from doublecortin knockout mice

Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A)

Mutations in the β-tubulin gene TUBB2B result in asymmetrical polymicrogyria

Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypes

Magnetic resonance imaging and histological studies of corpus callosal and hippocampal abnormalities linked to doublecortin deficiency

Novel Target Sequences for Pax-6 in the Brain-specific Activating Regions of the Rat Aldolase C Gene

Alternative Transcripts of Dclk1 and Dclk2 and Their Expression in Doublecortin Knockout Mice

Mutations in the [beta]-tubulin gene TUBB2B result in asymmetrical polymicrogyria

Human disorders of cortical development: from past to present

Mutations du gène EML1/Eml1 , progéniteurs neuronaux et hétérotopies chez l’homme et la souris

Correction: Mutation of the Diamond-Blackfan Anemia Gene Rps7 in Mouse Results in Morphological and Neuroanatomical Phenotypes

Branching and nucleokinesis defects in migrating interneurons derived from doublecortin knockout mice

REVIEW ARTICLE: Human disorders of cortical development: from past to present

Mutations in Eml1/EML1 lead to ectopic progenitors and neuronal heterotopia in mouse and human

Metabolism of proline in a human leukemic lymphoblastoid cell line

Bidirectional activity and orientation-dependent specificity of the rat aldolase C promoter in transgenic mice

High tyrosine kinase activity in normal nonproliferating cells

DEFICIT OF SUPPRESSOR T CELLS IN ACTIVE MULTIPLE SCLEROSIS

Upstream elements involved in vivo in activation of the brain-specific rat aldolase C gene. Role of binding sites for POU and winged helix proteins

Functional dissection of the brain-specific rat aldolase C gene promoter in transgenic mice. Essential role of two GC-rich boxes and an HNF3 binding site

CC Ar GG boxes, cis-acting elements with a dual specificity. Muscle-specific transcriptional activation and serum responsiveness

Functional Dissection of the Brain-specific Rat Aldolase C Gene Promoter in Transgenic Mice

Muscle-Specific Transcriptional Activation by CArG Box Requires Either Homophilic or Heterophilic Interactions of the CArG Box Binding Factors

Activation of Gene Expression via CArG Boxes during Myogenic Differentiation

Suchergebnisse filtern