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...

Targeted Deletion in Astrocyte Intermediate Filament (Gfap) Alters Neuronal Physiology

Proceedings of the National Academy of Sciences - PNAS, 1996-06, Vol.93 (13), p.6361-6366

1996

Volltextzugriff (PDF)

Analysis of the Zebrafish perplexed Mutation Reveals Tissue-Specific Roles for de Novo Pyrimidine Synthesis During Development

Genetics (Austin), 2005-08, Vol.170 (4), p.1827-1837

2005

Volltextzugriff (PDF)

A role for nyctalopin, a small leucine-rich repeat protein, in localizing the TRP melastatin 1 channel to retinal depolarizing bipolar cell dendrites

The Journal of neuroscience, 2011-07, Vol.31 (27), p.10060-10066

2011

Volltextzugriff (PDF)

A naturally occurring mouse model of X-linked congenital stationary night blindness

Investigative ophthalmology & visual science, 1998-11, Vol.39 (12), p.2443-2449

1998

Volltextzugriff (PDF)

Cardiac Troponin I Gene Knockout: A Mouse Model of Myocardial Troponin I Deficiency

Circulation research, 1999-01, Vol.84 (1), p.1-8

1999

Volltextzugriff (PDF)

pigk Mutation underlies macho behavior and affects Rohon-Beard cell excitability

Journal of neurophysiology, 2015-08, Vol.114 (2), p.1146-1157

2015

Volltextzugriff (PDF)

Newborn screening for cystic fibrosis in Wisconsin: comparison of biochemical and molecular methods

Pediatrics (Evanston), 1997-06, Vol.99 (6), p.819-824

1997

Volltextzugriff (PDF)

A calcium channel mutation causing hypokalemic periodic paralysis

Human molecular genetics, 1994-08, Vol.3 (8), p.1415-1419

1994

Volltextzugriff (PDF)

Genetic localization of an autosomal dominant leukodystrophy mimicking chronic progressive multiple sclerosis to chromosome 5q31

Human molecular genetics, 2000-03, Vol.9 (5), p.787-793

2000

Volltextzugriff (PDF)

Genetic heterogeneity in families with hereditary multiple exostoses

American journal of human genetics, 1993-07, Vol.53 (1), p.71-79

1993

Volltextzugriff (PDF)

Zebrafish (Danio rerio) exhibit individual differences in risk-taking behavior during predator inspection

Ethology, ecology & evolution, 2005, Vol.17 (1), p.77-81

2005

Volltextzugriff (PDF)

Morphological and Physiological Consequences of the Selective Elimination of Rod Photoreceptors in Transgenic Mice

Experimental eye research, 1996-07, Vol.63 (1), p.35-49

1996

Volltextzugriff (PDF)

Skeletal muscle and brain isoforms of a beta-subunit of human voltage-dependent calcium channels are encoded by a single gene

The Journal of biological chemistry, 1992-11, Vol.267 (32), p.22967-22972

1992

Volltextzugriff (PDF)

Positional Cloning of the young Mutation Identifies an Essential Role for the Brahma Chromatin Remodeling Complex in Mediating Retinal Cell Differentiation

Proceedings of the National Academy of Sciences - PNAS, 2003-05, Vol.100 (11), p.6535-6540

2003

Volltextzugriff (PDF)

Application of DNA analysis in a population-screening program for neonatal diagnosis of cystic fibrosis (CF) : comparison of screening protocols

American journal of human genetics, 1993-03, Vol.52 (3), p.616-626

1993

Volltextzugriff (PDF)

Regulatory Elements in the Introns of the Human HPRT Gene are Necessary for Its Expression in Embryonic Stem Cells

Proceedings of the National Academy of Sciences - PNAS, 1990-06, Vol.87 (11), p.4299-4303

1990

Volltextzugriff (PDF)

Localization of the Mouse nob (no b-wave) Gene to the Centromeric Region of the X Chromosome

Investigative ophthalmology & visual science, 1999-10, Vol.40 (11), p.2748-2751

1999

Volltextzugriff (PDF)

Molecular characterization of the gene encoding the gamma subunit of the human skeletal muscle 1,4-dihydropyridine-sensitive Ca2+ channel (CACNLG), cDNA sequence, gene structure, and chromosomal location

The Journal of biological chemistry, 1993-05, Vol.268 (13), p.9275-9279

1993

Volltextzugriff (PDF)

Localization of a Non-Specific X-linked Mental Retardation Gene, MRX23, to Xq23–q24

Human molecular genetics, 1996-03, Vol.5 (3), p.411-414

1996

Volltextzugriff (PDF)

A Cysteine-for-Arginine Substitution (R614C) in the Human Skeletal Muscle Calcium Release Channel Cosegregates With Malignant Hyperthermia

Anesthesia and analgesia, 1992-09, Vol.75 (3), p.441-448

1992

Volltextzugriff (PDF)

Refined genetic localization for central core disease

American journal of human genetics, 1993-02, Vol.52 (2), p.398-405

1993

Volltextzugriff (PDF)

Targetted correction of a mutant HPRT gene in mouse embryonic stem cells

Nature (London), 1987-12, Vol.330 (6148), p.576-578

1987

Volltextzugriff (PDF)

Efficient transformation and frequent single-site, single-copy insertion of DNA can be obtained in mouse erythroleukemia cells transformed by electroporation

Experimental hematology, 1986-11, Vol.14 (10), p.988

1986

Volltextzugriff (PDF)

Regulated Expression of Genes Inserted at the Human Chromosomal β -globin Locus by Homologous Recombination

Proceedings of the National Academy of Sciences - PNAS, 1988-06, Vol.85 (11), p.3845-3849

1988

Volltextzugriff (PDF)

Selected Minnesota Multiphasic Personality Inventory-2 Scales for Identifying Women with a History of Sexual Abuse

The journal of nervous and mental disease, 1995-01, Vol.183 (1), p.53-55

1995

Volltextzugriff (PDF)

1 – 25 von 3.279

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(2.903)
Mit Volltextzugriff
(2.776)

Publikationsform

2 weitere anzeigen...

Weniger anzeigen...

Sprache

2 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Science & Technology
(2.512)
Life Sciences & Biomedicine
(1.965)
Humans
(1.400)
Biological And Medical Sciences
(952)
Female
(925)
Male
(873)
Medical Sciences
(714)
Animals
(596)
Middle Aged
(552)
Aged
(459)
Cardiovascular System & Cardiology
(401)
Physical Sciences
(400)
Cardiac & Cardiovascular Systems
(388)
Adult
(382)
Technology
(285)
Fundamental And Applied Biological Sciences. Psychology
(254)
Treatment Outcome
(228)
Mice
(210)
Biochemistry & Molecular Biology
(189)
Cardiology. Vascular System
(169)

15 weitere anzeigen...

Weniger anzeigen...

Kollektion

MEDLINE
(1.938)
Ingenta.com
(1.445)
EZB Electronic Journals Library
(1.319)
WK Lippincott Williams & Wilkins–Connect here FIRST to enable access
(1.243)
NUS Single-Journal Subscriptions
(940)
Elsevier ScienceDirect Journals
(801)
Elsevier Journal Backfiles on ScienceDirect (DFG Nationallizenzen)
(576)
IngentaConnect Journals
(485)
Wiley Online Library E-Journals
(403)
Wiley Online Library Full Collection 2018
(308)
JSTOR All Journals
(242)
SpringerLink
(145)
Oxford Journals
(144)
IEEE Xplore
(134)
Taylor & Francis Journals
(122)
Taylor & Francis
(104)
SpringerLINK Contemporary (Konsortium Baden-Württemberg)
(100)
Taylor & Francis:Master (3349 titles)
(99)
Oxford Journals 2020 Medicine
(99)
SAGE Journals
(65)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

Targeted Deletion in Astrocyte Intermediate Filament (Gfap) Alters Neuronal Physiology

Analysis of the Zebrafish perplexed Mutation Reveals Tissue-Specific Roles for de Novo Pyrimidine Synthesis During Development

A role for nyctalopin, a small leucine-rich repeat protein, in localizing the TRP melastatin 1 channel to retinal depolarizing bipolar cell dendrites

A naturally occurring mouse model of X-linked congenital stationary night blindness

Cardiac Troponin I Gene Knockout: A Mouse Model of Myocardial Troponin I Deficiency

pigk Mutation underlies macho behavior and affects Rohon-Beard cell excitability

Newborn screening for cystic fibrosis in Wisconsin: comparison of biochemical and molecular methods

A calcium channel mutation causing hypokalemic periodic paralysis

Genetic localization of an autosomal dominant leukodystrophy mimicking chronic progressive multiple sclerosis to chromosome 5q31

Genetic heterogeneity in families with hereditary multiple exostoses

Zebrafish (Danio rerio) exhibit individual differences in risk-taking behavior during predator inspection

Morphological and Physiological Consequences of the Selective Elimination of Rod Photoreceptors in Transgenic Mice

Skeletal muscle and brain isoforms of a beta-subunit of human voltage-dependent calcium channels are encoded by a single gene

Positional Cloning of the young Mutation Identifies an Essential Role for the Brahma Chromatin Remodeling Complex in Mediating Retinal Cell Differentiation

Application of DNA analysis in a population-screening program for neonatal diagnosis of cystic fibrosis (CF) : comparison of screening protocols

Regulatory Elements in the Introns of the Human HPRT Gene are Necessary for Its Expression in Embryonic Stem Cells

Localization of the Mouse nob (no b-wave) Gene to the Centromeric Region of the X Chromosome

Molecular characterization of the gene encoding the gamma subunit of the human skeletal muscle 1,4-dihydropyridine-sensitive Ca2+ channel (CACNLG), cDNA sequence, gene structure, and chromosomal location

Localization of a Non-Specific X-linked Mental Retardation Gene, MRX23, to Xq23–q24

A Cysteine-for-Arginine Substitution (R614C) in the Human Skeletal Muscle Calcium Release Channel Cosegregates With Malignant Hyperthermia

Refined genetic localization for central core disease

Targetted correction of a mutant HPRT gene in mouse embryonic stem cells

Efficient transformation and frequent single-site, single-copy insertion of DNA can be obtained in mouse erythroleukemia cells transformed by electroporation

Regulated Expression of Genes Inserted at the Human Chromosomal β -globin Locus by Homologous Recombination

Selected Minnesota Multiphasic Personality Inventory-2 Scales for Identifying Women with a History of Sexual Abuse

Suchergebnisse filtern