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...

Autism-relevant social abnormalities and cognitive deficits in engrailed-2 knockout mice

PloS one, 2012-07, Vol.7 (7), p.e40914-e40914

2012

Volltextzugriff (PDF)

Congenital Cataract in Gpr161vl/vl Mice Is Modified by Proximal Chromosome 15

PloS one, 2017, Vol.12 (1), p.e0170724-e0170724

2017

Volltextzugriff (PDF)

Autism associated gene, engrailed2, and flanking gene levels are altered in post-mortem cerebellum

PloS one, 2014-02, Vol.9 (2), p.e87208-e87208

2014

Volltextzugriff (PDF)

Chronic desipramine treatment rescues depression‐related, social and cognitive deficits in Engrailed‐2 knockout mice

Genes, brain and behavior, 2014-03, Vol.13 (3), p.286-298

2014

Volltextzugriff (PDF)

The Dlk1 and Gtl2 genes are linked and reciprocally imprinted

Genes & development, 2000-08, Vol.14 (16), p.1997-2002

2000

Volltextzugriff (PDF)

Cut-like homeobox 1 and nuclear factor I/B mediate ENGRAILED2 autism spectrum disorder-associated haplotype function

Human molecular genetics, 2012-04, Vol.21 (7), p.1566-1580

2012

Volltextzugriff (PDF)

Identification of a Schizophrenia-Associated Functional Noncoding Variant in NOS1AP

The American journal of psychiatry, 2009-04, Vol.166 (4), p.434-441

2009

Volltextzugriff (PDF)

orphan G protein-coupled receptor, Gpr161, encodes the vacuolated lens locus and controls neurulation and lens development

Proceedings of the National Academy of Sciences - PNAS, 2008-02, Vol.105 (6), p.2088-2093

2008

Volltextzugriff (PDF)

Chronic Enzyme Replacement to the Brain of a Late Infantile Neuronal Ceroid Lipofuscinosis Mouse Has Differential Effects on Phenotypes of Disease

Molecular therapy. Methods & clinical development, 2017-03, Vol.4 (C), p.204-212

2017

Volltextzugriff (PDF)

The construct and concurrent validity of brief standing sway assessments in children with and without cerebral palsy

Gait & posture, 2021-02, Vol.84, p.293-299

2021

Volltextzugriff (PDF)

Engrailed-2 (En2) deletion produces multiple neurodevelopmental defects in monoamine systems, forebrain structures and neurogenesis and behavior

Human molecular genetics, 2015-10, Vol.24 (20), p.5805-5827

2015

Volltextzugriff (PDF)

The orphan GPCR, Gpr161, regulates the retinoic acid and canonical Wnt pathways during neurulation

Developmental biology, 2015-06, Vol.402 (1), p.17-31

2015

Volltextzugriff (PDF)

Autism-Associated Haplotype Affects the Regulation of the Homeobox Gene, ENGRAILED 2

Biological psychiatry (1969), 2009-11, Vol.66 (10), p.911-917

2009

Volltextzugriff (PDF)

Quantitative Measurement of Relative Retinoic Acid Levels in E8.5 Embryos and Neurosphere Cultures Using the F9 RARE-Lacz Cell-based Reporter Assay

Journal of visualized experiments, 2016-09 (115)

2016

Volltextzugriff (PDF)

NOS1AP protein levels are altered in BA46 and cerebellum of patients with schizophrenia

Schizophrenia research, 2010-12, Vol.124 (1), p.248-250

2010

Volltextzugriff (PDF)

Genomic imprinting of a placental lactogen gene in Peromyscus

Development genes and evolution, 2001-12, Vol.211 (11), p.523-532

2001

Volltextzugriff (PDF)

Quantitative trait loci affecting phenotypic variation in the vacuolated lens mouse mutant, a multigenic mouse model of neural tube defects

Physiological genomics, 2008-11, Vol.35 (3), p.296-304

2008

Volltextzugriff (PDF)

Congenital Cataract in Gpr161.sup.vl/vl Mice Is Modified by Proximal Chromosome 15

PloS one, 2017-01, Vol.12 (1), p.e0170724

2017

Volltextzugriff (PDF)

Nondisjunction rates and abnormal embryonic development in a mouse cross between heterozygotes carrying a (7, 18) robertsonian translocation chromosome

Genetics (Austin), 1995-10, Vol.141 (2), p.667-674

1995

Volltextzugriff (PDF)

Quantitative Measurement of Relative Retinoic Acid Levels in E8.5 Embryos and Neurosphere Cultures Using the F9 RARE-Lacz Cell-based Reporter Assay

Journal of visualized experiments, 2016-09 (115)

2016

Volltextzugriff (PDF)

A high-resolution linkage map of the lethal spotting locus: a mouse model for Hirschsprung disease

Mammalian genome, 1995-01, Vol.6 (1), p.1-7

1995

Volltextzugriff (PDF)

Counterion effects on the aqueous solution viscosity of cationic surfactants

Journal of the American Oil Chemists' Society, 1986-12, Vol.63 (12), p.1586-1589

1986

Volltextzugriff (PDF)

Autism Associated Gene, ENGRAILED2, and Flanking Gene Levels Are Altered in Post-Mortem Cerebellum: e87208

PloS one, 2014-02, Vol.9 (2)

2014

Volltextzugriff (PDF)

Degeneration of the Eyes of Tyrosine-Deficient Chick Embryos

Science (American Association for the Advancement of Science), 1965-06, Vol.148 (3678), p.1743-1745

1965

Volltextzugriff (PDF)

Physician education in human sexuality

The Journal of family practice, 1984-11, Vol.19 (5), p.683-684

1984

Volltextzugriff (PDF)

1 – 25 von 426

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(377)
Mit Volltextzugriff
(337)

Publikationsform

Sprache

Englisch
(424)
Japanisch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(280)
Life Sciences & Biomedicine
(182)
Humans
(169)
Female
(111)
Male
(87)
Rheumatology
(75)
Physical Sciences
(72)
Biological And Medical Sciences
(67)
Middle Aged
(67)
Medical Sciences
(63)
Adult
(61)
Aged
(48)
Astronomy & Astrophysics
(37)
Animals
(30)
Diseases Of The Osteoarticular System
(26)
Treatment Outcome
(25)
Obstetrics & Gynecology
(23)
Aged, 80 And Over
(22)
Chemistry
(21)
General & Internal Medicine
(21)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Autism-relevant social abnormalities and cognitive deficits in engrailed-2 knockout mice

Congenital Cataract in Gpr161vl/vl Mice Is Modified by Proximal Chromosome 15

Autism associated gene, engrailed2, and flanking gene levels are altered in post-mortem cerebellum

Chronic desipramine treatment rescues depression‐related, social and cognitive deficits in Engrailed‐2 knockout mice

The Dlk1 and Gtl2 genes are linked and reciprocally imprinted

Cut-like homeobox 1 and nuclear factor I/B mediate ENGRAILED2 autism spectrum disorder-associated haplotype function

Identification of a Schizophrenia-Associated Functional Noncoding Variant in NOS1AP

orphan G protein-coupled receptor, Gpr161, encodes the vacuolated lens locus and controls neurulation and lens development

Chronic Enzyme Replacement to the Brain of a Late Infantile Neuronal Ceroid Lipofuscinosis Mouse Has Differential Effects on Phenotypes of Disease

The construct and concurrent validity of brief standing sway assessments in children with and without cerebral palsy

Engrailed-2 (En2) deletion produces multiple neurodevelopmental defects in monoamine systems, forebrain structures and neurogenesis and behavior

The orphan GPCR, Gpr161, regulates the retinoic acid and canonical Wnt pathways during neurulation

Autism-Associated Haplotype Affects the Regulation of the Homeobox Gene, ENGRAILED 2

Quantitative Measurement of Relative Retinoic Acid Levels in E8.5 Embryos and Neurosphere Cultures Using the F9 RARE-Lacz Cell-based Reporter Assay

NOS1AP protein levels are altered in BA46 and cerebellum of patients with schizophrenia

Genomic imprinting of a placental lactogen gene in Peromyscus

Quantitative trait loci affecting phenotypic variation in the vacuolated lens mouse mutant, a multigenic mouse model of neural tube defects

Congenital Cataract in Gpr161.sup.vl/vl Mice Is Modified by Proximal Chromosome 15

Nondisjunction rates and abnormal embryonic development in a mouse cross between heterozygotes carrying a (7, 18) robertsonian translocation chromosome

Quantitative Measurement of Relative Retinoic Acid Levels in E8.5 Embryos and Neurosphere Cultures Using the F9 RARE-Lacz Cell-based Reporter Assay

A high-resolution linkage map of the lethal spotting locus: a mouse model for Hirschsprung disease

Counterion effects on the aqueous solution viscosity of cationic surfactants

Autism Associated Gene, ENGRAILED2, and Flanking Gene Levels Are Altered in Post-Mortem Cerebellum: e87208

Degeneration of the Eyes of Tyrosine-Deficient Chick Embryos

Physician education in human sexuality

Suchergebnisse filtern