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...

Disruption of the Serine/Threonine Kinase 9 Gene Causes Severe X-Linked Infantile Spasms and Mental Retardation

American journal of human genetics, 2003-06, Vol.72 (6), p.1401-1411

2003

Volltextzugriff (PDF)

Fcα/μ receptor mediates endocytosis of IgM-coated microbes

Nature immunology, 2000-11, Vol.1 (5), p.441-446

2000

Volltextzugriff (PDF)

Cutting Edge: Human 2B4, an Activating NK Cell Receptor, Recruits the Protein Tyrosine Phosphatase SHP-2 and the Adaptor Signaling Protein SAP

The Journal of immunology (1950), 1999-06, Vol.162 (12), p.6981-6985

1999

Volltextzugriff (PDF)

LAIR-1, a Novel Inhibitory Receptor Expressed on Human Mononuclear Leukocytes

Immunity (Cambridge, Mass.), 1997-08, Vol.7 (2), p.283-290

1997

Volltextzugriff (PDF)

Myeloid DAP12-Associating Lectin (MDL)-1 Is a Cell Surface Receptor Involved in the Activation of Myeloid Cells

Proceedings of the National Academy of Sciences - PNAS, 1999-08, Vol.96 (17), p.9792-9796

1999

Volltextzugriff (PDF)

The History and Development of the Human Genetics Society of Australasia

Twin research and human genetics, 2008-08, Vol.11 (4), p.363-367

Sutherland, Grant R.

2008

Volltextzugriff (PDF)

Human Chromosomal Fragile Site FRA16B Is an Amplified AT-Rich Minisatellite Repeat

Cell, 1997-02, Vol.88 (3), p.367-374

1997

Volltextzugriff (PDF)

MUC13, a Novel Human Cell Surface Mucin Expressed by Epithelial and Hemopoietic Cells

The Journal of biological chemistry, 2001-05, Vol.276 (21), p.18327-18336

2001

Volltextzugriff (PDF)

HLS5, a Novel RBCC (Ring Finger, B Box, Coiled-coil) Family Member Isolated from a Hemopoietic Lineage Switch, Is a Candidate Tumor Suppressor

The Journal of biological chemistry, 2004-02, Vol.279 (9), p.8181-8189

2004

Volltextzugriff (PDF)

A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

Nature genetics, 1995-10, Vol.11 (2), p.201-203

1995

Volltextzugriff (PDF)

The molecular basis of fragile sites in human chromosomes

Current opinion in genetics & development, 1995-06, Vol.5 (3), p.323-327

1995

Volltextzugriff (PDF)

Two novel mucin genes down-regulated in colorectal cancer identified by differential display

Cancer research (Chicago, Ill.), 1999-08, Vol.59 (16), p.4083-4089

1999

Volltextzugriff (PDF)

Simple Tandem DNA Repeats and Human Genetic Disease

Proceedings of the National Academy of Sciences - PNAS, 1995-04, Vol.92 (9), p.3636-3641

1995

Volltextzugriff (PDF)

Isolation and identification of homeobox genes from the human placenta including a novel member of the Distal-less family, DLX4

Gene, 1997-03, Vol.187 (1), p.55-61

1997

Volltextzugriff (PDF)

Fragile sites still breaking

Trends in Genetics, 1998-12, Vol.14 (12), p.501-506

1998

Volltextzugriff (PDF)

Simple repeat DNA is not replicated simply

Nature genetics, 1994-02, Vol.6 (2), p.114-116

1994

Volltextzugriff (PDF)

Aberrant CBFA2T3B gene promoter methylation in breast tumors

Molecular cancer, 2004-08, Vol.3 (1), p.22-22

2004

Volltextzugriff (PDF)

Identification of a Novel Human Tankyrase through Its Interaction with the Adaptor Protein Grb14

The Journal of biological chemistry, 2001-05, Vol.276 (20), p.17172-17180

2001

Volltextzugriff (PDF)

Cloning, characterization, and chromosomal location of a novel human K+-Cl- cotransporter

The Journal of biological chemistry, 1999-04, Vol.274 (15), p.10661-10667

1999

Volltextzugriff (PDF)

At least two different regions are involved in allelic imbalance on chromosome arm 16q in breast cancer

Genes chromosomes & cancer, 1994-02, Vol.9 (2), p.101-107

1994

Volltextzugriff (PDF)

HPP1: A Transmembrane Protein-Encoding Gene Commonly Methylated in Colorectal Polyps and Cancers

Proceedings of the National Academy of Sciences - PNAS, 2001-01, Vol.98 (1), p.265-270

2001

Volltextzugriff (PDF)

Deletion of Glu155 causes a deficiency of glutathione transferase Omega 1-1 but does not alter sensitivity to arsenic trioxide and other cytotoxic drugs

The international journal of biochemistry & cell biology, 2008, Vol.40 (11), p.2553-2559

2008

Volltextzugriff (PDF)

Molecular cloning of a novel human PAPS synthetase which is differentially expressed in metastatic and non-metastatic colon carcinoma cells

The international journal of biochemistry & cell biology, 1999-05, Vol.31 (5), p.613-626

1999

Volltextzugriff (PDF)

Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein

Genomics (San Diego, Calif.), 2004-07, Vol.84 (1), p.69-81

2004

Volltextzugriff (PDF)

1 – 25 von 261

Suche als RSS-Feed

Aktive Filter

ThemaMale

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(233)
Mit Volltextzugriff
(219)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Englisch
(259)
Deutsch
(1)
Japanisch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(157)
Humans
(152)
Life Sciences & Biomedicine
(147)
Biological And Medical Sciences
(83)
Molecular Sequence Data
(65)
Genetics & Heredity
(61)
Base Sequence
(57)
Chromosome Mapping
(54)
Medical Sciences
(51)
Amino Acid Sequence
(46)
Animals
(45)
Cloning, Molecular
(38)
Biochemistry & Molecular Biology
(36)
Fundamental And Applied Biological Sciences. Psychology
(34)
Female
(31)
Mice
(30)
Chromosome Fragility
(21)
Molecular And Cellular Biology
(21)
In Situ Hybridization, Fluorescence
(20)
Biotechnology & Applied Microbiology
(19)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Disruption of the Serine/Threonine Kinase 9 Gene Causes Severe X-Linked Infantile Spasms and Mental Retardation

Fcα/μ receptor mediates endocytosis of IgM-coated microbes

Cutting Edge: Human 2B4, an Activating NK Cell Receptor, Recruits the Protein Tyrosine Phosphatase SHP-2 and the Adaptor Signaling Protein SAP

LAIR-1, a Novel Inhibitory Receptor Expressed on Human Mononuclear Leukocytes

Myeloid DAP12-Associating Lectin (MDL)-1 Is a Cell Surface Receptor Involved in the Activation of Myeloid Cells

The History and Development of the Human Genetics Society of Australasia

Human Chromosomal Fragile Site FRA16B Is an Amplified AT-Rich Minisatellite Repeat

MUC13, a Novel Human Cell Surface Mucin Expressed by Epithelial and Hemopoietic Cells

HLS5, a Novel RBCC (Ring Finger, B Box, Coiled-coil) Family Member Isolated from a Hemopoietic Lineage Switch, Is a Candidate Tumor Suppressor

A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

The molecular basis of fragile sites in human chromosomes

Two novel mucin genes down-regulated in colorectal cancer identified by differential display

Simple Tandem DNA Repeats and Human Genetic Disease

Isolation and identification of homeobox genes from the human placenta including a novel member of the Distal-less family, DLX4

Fragile sites still breaking

Simple repeat DNA is not replicated simply

Aberrant CBFA2T3B gene promoter methylation in breast tumors

Identification of a Novel Human Tankyrase through Its Interaction with the Adaptor Protein Grb14

Cloning, characterization, and chromosomal location of a novel human K+-Cl- cotransporter

At least two different regions are involved in allelic imbalance on chromosome arm 16q in breast cancer

HPP1: A Transmembrane Protein-Encoding Gene Commonly Methylated in Colorectal Polyps and Cancers

Deletion of Glu155 causes a deficiency of glutathione transferase Omega 1-1 but does not alter sensitivity to arsenic trioxide and other cytotoxic drugs

Molecular cloning of a novel human PAPS synthetase which is differentially expressed in metastatic and non-metastatic colon carcinoma cells

Positional cloning of the Fanconi anaemia group A gene

Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein

Aktive Filter

Suchergebnisse filtern