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...

ARX polyalanine expansion mutations lead to migration impediment in the rostral cortex coupled with a developmental deficit of calbindin positive cortical GABAergic interneurons

Neuroscience, 2017-08, Vol.357, p.220-231

2017

Volltextzugriff (PDF)

Incorrect dosage of IQSEC2, a known intellectual disability and epilepsy gene, disrupts dendritic spine morphogenesis

Translational psychiatry, 2017-05, Vol.7 (5), p.e1110-e1110

2017

Volltextzugriff (PDF)

Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability

Molecular psychiatry, 2012-11, Vol.17 (11), p.1103-1115

2012

Volltextzugriff (PDF)

Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autism

Molecular psychiatry, 2010-07, Vol.15 (7), p.767-776

2010

Volltextzugriff (PDF)

Aristaless -related homeobox gene, the gene responsible for West syndrome and related disorders, is a Groucho/transducin-like enhancer of split dependent transcriptional repressor

Neuroscience, 2007-04, Vol.146 (1), p.236-247

2007

Volltextzugriff (PDF)

Screening and cell-based assessment of mutations in the Aristaless-related homeobox (ARX) gene

Clinical genetics, 2011-12, Vol.80 (6), p.510-522

2011

Volltextzugriff (PDF)

The genetic landscape of intellectual disability arising from chromosome X

Trends in genetics, 2009-07, Vol.25 (7), p.308-316

2009

Volltextzugriff (PDF)

OP15 – 2728: The epileptic encephalopathy of IQSEC2 mutations

European journal of paediatric neurology, 2015-05, Vol.19, p.S5-S6

2015

Volltextzugriff (PDF)

Preferential Intestinal Delivery of Long[Arg3] Insulin-Like Growth Factor (LR3IGF-I) over IGF-I in Preweaning and Adult Rats

Endocrinology (Philadelphia), 2003-05, Vol.144 (5), p.1887-1893

2003

Volltextzugriff (PDF)

ARX homeodomain mutations abolish DNA binding and lead to a loss of transcriptional repression

Human molecular genetics, 2012-04, Vol.21 (7), p.1639-1647

2012

Volltextzugriff (PDF)

IGFBP mRNA expression in small intestine of rat during postnatal development

American journal of physiology: Gastrointestinal and liver physiology, 2001-12, Vol.281 (6), p.G1378-G1384

2001

Volltextzugriff (PDF)

Degradation of IGF-I in the adult rat gastrointestinal tract is limited by a specific antiserum or the dietary protein casein

Journal of endocrinology, 1995-08, Vol.146 (2), p.215-225

1995

Volltextzugriff (PDF)

Systemic infusion of IGF-I or LR(3)IGF-I stimulates visceral organ growth and proliferation of gut tissues in suckling rats

American journal of physiology: Gastrointestinal and liver physiology, 1997-03, Vol.272 (3 Pt 1), p.G522-G533

1997

Volltextzugriff (PDF)

IGFBP mRNA expression in small intestine of rat during postnatal development

American journal of physiology: Gastrointestinal and liver physiology, 2001-12, Vol.44 (6), p.G1378-G1384

2001

Volltextzugriff (PDF)

Systemically but not orogastrically delivered insulin-like growth factor (IGF)-I and long [Arg3]IGF-I stimulates intestinal disaccharidase activity in two age groups of suckling rats

Pediatric research, 1998-11, Vol.44 (5), p.663-672

1998

Volltextzugriff (PDF)

Molecular pathology of expanded polyalanine tract mutations in the Aristaless-related homeobox gene

Genomics (San Diego, Calif.), 2007-07, Vol.90 (1), p.59-71

2007

Volltextzugriff (PDF)

Enhancement of intestinal growth and repair by growth factors

Current Opinion in Pharmacology, 2001-12, Vol.1 (6), p.568-574

2001

Volltextzugriff (PDF)

Systemic infusion of IGF-I or LR3IGF-I stimulates visceral organ growth and proliferation of gut tissues in suckling rats

American journal of physiology: Gastrointestinal and liver physiology, 1997-03, Vol.35 (3), p.G522-G533

1997

Volltextzugriff (PDF)

Production of a human epidermal growth factor fusion protein and its degradation in rat gastrointestinal flushings

Journal of molecular endocrinology, 1996-02, Vol.16 (1), p.89-97

1996

Volltextzugriff (PDF)

The human mitochondrial translation factor TACO1 alleviates mitoribosome stalling at polyproline stretches

Nucleic acids research, 2024-09, Vol.52 (16), p.9710-9726

2024

Volltextzugriff (PDF)

CHCHD10P80L knock-in zebrafish display a mild ALS-like phenotype

Experimental neurology, 2024-12, Vol.382, p.114945, Article 114945

2024

Volltextzugriff (PDF)

Human SCO2 is required for the synthesis of CO II and as a thiol-disulphide oxidoreductase for SCO1

Human molecular genetics, 2009-06, Vol.18 (12), p.2230-2240

2009

Volltextzugriff (PDF)

Mutations in ABCD4 cause a new inborn error of vitamin B12 metabolism

Nature genetics, 2012-10, Vol.44 (10), p.1152-1155

2012

Volltextzugriff (PDF)

Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type

Nature genetics, 2006-01, Vol.38 (1), p.93-100

2006

Volltextzugriff (PDF)

Tissue-specific selection for different mtDNA genotypes in heteroplasmic mice

Nature genetics, 1997-05, Vol.16 (1), p.93-95

1997

Volltextzugriff (PDF)

1 – 25 von 102

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(98)
Mit Volltextzugriff
(84)

Publikationsform

Artikel
(101)
Berichte
(1)

Sprache

Englisch
(102)

Erscheinungsjahr

n.n

Thema

Science & Technology
(69)
Life Sciences & Biomedicine
(67)
Humans
(63)
Biological And Medical Sciences
(36)
Mutation
(35)
Genetics & Heredity
(31)
Female
(30)
Animals
(26)
Male
(26)
Medical Sciences
(23)
Fundamental And Applied Biological Sciences. Psychology
(19)
Biochemistry & Molecular Biology
(16)
Mitochondria - Metabolism
(15)
Neurosciences & Neurology
(14)
Genetics Of Eukaryotes. Biological And Molecular Evolution
(13)
Mice
(13)
Cell Line
(12)
Cells, Cultured
(11)
Neurology
(11)
Amino Acid Sequence
(10)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

ARX polyalanine expansion mutations lead to migration impediment in the rostral cortex coupled with a developmental deficit of calbindin positive cortical GABAergic interneurons

Incorrect dosage of IQSEC2, a known intellectual disability and epilepsy gene, disrupts dendritic spine morphogenesis

Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability

Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autism

Aristaless -related homeobox gene, the gene responsible for West syndrome and related disorders, is a Groucho/transducin-like enhancer of split dependent transcriptional repressor

Screening and cell-based assessment of mutations in the Aristaless-related homeobox (ARX) gene

The genetic landscape of intellectual disability arising from chromosome X

OP15 – 2728: The epileptic encephalopathy of IQSEC2 mutations

Preferential Intestinal Delivery of Long[Arg3] Insulin-Like Growth Factor (LR3IGF-I) over IGF-I in Preweaning and Adult Rats

ARX homeodomain mutations abolish DNA binding and lead to a loss of transcriptional repression

IGFBP mRNA expression in small intestine of rat during postnatal development

Degradation of IGF-I in the adult rat gastrointestinal tract is limited by a specific antiserum or the dietary protein casein

Systemic infusion of IGF-I or LR(3)IGF-I stimulates visceral organ growth and proliferation of gut tissues in suckling rats

IGFBP mRNA expression in small intestine of rat during postnatal development

Systemically but not orogastrically delivered insulin-like growth factor (IGF)-I and long [Arg3]IGF-I stimulates intestinal disaccharidase activity in two age groups of suckling rats

Molecular pathology of expanded polyalanine tract mutations in the Aristaless-related homeobox gene

Enhancement of intestinal growth and repair by growth factors

Systemic infusion of IGF-I or LR3IGF-I stimulates visceral organ growth and proliferation of gut tissues in suckling rats

Production of a human epidermal growth factor fusion protein and its degradation in rat gastrointestinal flushings

The human mitochondrial translation factor TACO1 alleviates mitoribosome stalling at polyproline stretches

CHCHD10P80L knock-in zebrafish display a mild ALS-like phenotype

Human SCO2 is required for the synthesis of CO II and as a thiol-disulphide oxidoreductase for SCO1

Mutations in ABCD4 cause a new inborn error of vitamin B12 metabolism

Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type

Tissue-specific selection for different mtDNA genotypes in heteroplasmic mice

Suchergebnisse filtern