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...

Dictyostelium nucleoside diphosphate kinase highly homologous to Nm23 and awd proteins involved in mammalian tumor metastasis and Drosophila development

JNCI : Journal of the National Cancer Institute, 1990-07, Vol.82 (14), p.1199-1202

1990

Volltextzugriff (PDF)

Nucleoside diphosphate kinase/NM23 expression in breast cancer: Lack of correlation with lymph‐node metastasis

International journal of cancer, 1992-02, Vol.50 (4), p.533-538

1992

Volltextzugriff (PDF)

Overexpression of nm23-H1 and nm23-H2 genes in colorectal carcinomas and loss of nm23-H1 expression in advanced tumour stages

Gut, 1995-11, Vol.37 (5), p.712-720

1995

Volltextzugriff (PDF)

Nucleoside diphosphate kinases as potential new targets for control of development and cancer

Trends in pharmacological sciences (Regular ed.), 1992, Vol.13 (2), p.46-48

1992

Volltextzugriff (PDF)

Overexpression of Insulin Receptor Substrate-2 in Human and Murine Hepatocellular Carcinoma

The American journal of pathology, 2005-09, Vol.167 (3), p.869-877

2005

Volltextzugriff (PDF)

Increased Lung Metastasis in Transgenic NM23-Null/SV40 Mice with Hepatocellular Carcinoma

JNCI : Journal of the National Cancer Institute, 2005-06, Vol.97 (11), p.836-845

2005

Volltextzugriff (PDF)

Progressive Osseous Heteroplasia: A Model for the Imprinting Effects of GNAS Inactivating Mutations in Humans

The journal of clinical endocrinology and metabolism, 2010-06, Vol.95 (6), p.3028-3038

2010

Volltextzugriff (PDF)

Five new TTF1/NKX2.1 mutations in brain–lung–thyroid syndrome: rescue by PAX8 synergism in one case

Human molecular genetics, 2009-06, Vol.18 (12), p.2266-2276

2009

Volltextzugriff (PDF)

Phase II study on gemcitabine in recurrent and/or metastatic adenoid cystic carcinoma of the head and neck (EORTC 24982)

European journal of cancer (1990), 2008-11, Vol.44 (17), p.2542-2545

2008

Volltextzugriff (PDF)

Phase I Clinical and Magnetic Resonance Imaging Study of the Vascular Agent NGR-hTNF in Patients with Advanced Cancers (European Organization for Research and Treatment of Cancer Study 16041)

Clinical cancer research, 2010-02, Vol.16 (4), p.1315-1323

2010

Volltextzugriff (PDF)

Leber’s optic neuropathy associated with disseminated white matter disease: A case report and review

Clinical neurology and neurosurgery, 2009-01, Vol.111 (1), p.83-86

2009

Volltextzugriff (PDF)

A second locus for Aicardi-Goutières syndrome at chromosome 13q14–21

Journal of medical genetics, 2006-05, Vol.43 (5), p.444-450

2006

Volltextzugriff (PDF)

Comparison of Remifentanil With Fentanyl for Deep Sedation in Oral Surgery

Journal of oral and maxillofacial surgery, 2006-02, Vol.64 (2), p.215-222

2006

Volltextzugriff (PDF)

Relapses of childhood anaplastic large-cell lymphoma: Treatment results in a series of 41 children - a report from the French Society of Pediatric Oncology

Annals of oncology, 2000-01, Vol.11 (1), p.53-58

2000

Volltextzugriff (PDF)

Methanol Adduct of Puupehenone, a Biologically Active Derivative from the Marine Sponge Hyrtios Species

Journal of natural products (Washington, D.C.), 1999-09, Vol.62 (9), p.1304-1305

1999

Volltextzugriff (PDF)

CD30+ anaplastic large-cell lymphoma in children : Analysis of 82 patients enrolled in two consecutive studies of the French society of Pediatric Oncology

Blood, 1998-11, Vol.92 (10), p.3591-3598

1998

Volltextzugriff (PDF)

Analysis of local-regional relapses in patients with early breast cancers treated by excision and radiotherapy: experience of the Institut Gustave-Roussy

International journal of radiation oncology, biology, physics, 1985, Vol.11 (1), p.137-145

1985

Volltextzugriff (PDF)

Enzyme replacement therapy and renal function in 201 patients with Fabry disease

Clinical nephrology, 2006-08, Vol.66 (2), p.77

2006

Volltextzugriff (PDF)

Increased paternal age in CHARGE association

Clinical genetics, 1996-12, Vol.50 (6), p.548-550

1996

Volltextzugriff (PDF)

CHARGE syndrome: Report of 47 cases and review

American journal of medical genetics, 1998-04, Vol.76 (5), p.402-409

1998

Volltextzugriff (PDF)

Short-term treatment by implantable pump does not impair lipoprotein pattern in IDDM patients

Transplantation proceedings, 1992-06, Vol.24 (3), p.947-947

1992

Volltextzugriff (PDF)

Hemoglobin Saverne: A New Variant with Elongated β Chains: Structural and Functional Properties

Hemoglobin, 1988, Vol.12 (4), p.337-352

1988

Volltextzugriff (PDF)

HB J-Cordoba [α2Aβ2 95 (FG2)LYS →MET] A New HB Variant Found in Argentina

Hemoglobin, 1988, Vol.12 (1), p.1-11

1988

Volltextzugriff (PDF)

Long segment and short segment familial Hirschprung's disease : variable clinical expression at the RET locus

Journal of medical genetics, 1994, Vol.31 (8), p.602-606

1994

Volltextzugriff (PDF)

1 – 25 von 28

Suche als RSS-Feed

Aktive Filter

ThemaMedical Sciences

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(24)
Mit Volltextzugriff
(24)

Publikationsform

Artikel
(28)

Sprache

Englisch
(28)

Erscheinungsjahr

n.n

Thema

14 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Dictyostelium nucleoside diphosphate kinase highly homologous to Nm23 and awd proteins involved in mammalian tumor metastasis and Drosophila development

Nucleoside diphosphate kinase/NM23 expression in breast cancer: Lack of correlation with lymph‐node metastasis

Overexpression of nm23-H1 and nm23-H2 genes in colorectal carcinomas and loss of nm23-H1 expression in advanced tumour stages

Nucleoside diphosphate kinases as potential new targets for control of development and cancer

Overexpression of Insulin Receptor Substrate-2 in Human and Murine Hepatocellular Carcinoma

Increased Lung Metastasis in Transgenic NM23-Null/SV40 Mice with Hepatocellular Carcinoma

Progressive Osseous Heteroplasia: A Model for the Imprinting Effects of GNAS Inactivating Mutations in Humans

Five new TTF1/NKX2.1 mutations in brain–lung–thyroid syndrome: rescue by PAX8 synergism in one case

Phase II study on gemcitabine in recurrent and/or metastatic adenoid cystic carcinoma of the head and neck (EORTC 24982)

Phase I Clinical and Magnetic Resonance Imaging Study of the Vascular Agent NGR-hTNF in Patients with Advanced Cancers (European Organization for Research and Treatment of Cancer Study 16041)

Leber’s optic neuropathy associated with disseminated white matter disease: A case report and review

A second locus for Aicardi-Goutières syndrome at chromosome 13q14–21

Comparison of Remifentanil With Fentanyl for Deep Sedation in Oral Surgery

Relapses of childhood anaplastic large-cell lymphoma: Treatment results in a series of 41 children - a report from the French Society of Pediatric Oncology

Methanol Adduct of Puupehenone, a Biologically Active Derivative from the Marine Sponge Hyrtios Species

CD30+ anaplastic large-cell lymphoma in children : Analysis of 82 patients enrolled in two consecutive studies of the French society of Pediatric Oncology

Analysis of local-regional relapses in patients with early breast cancers treated by excision and radiotherapy: experience of the Institut Gustave-Roussy

Enzyme replacement therapy and renal function in 201 patients with Fabry disease

Increased paternal age in CHARGE association

A proposed new contiguous gene syndrome on 8q consists of Branchio-Oto-Renal (BOR) syndrome, Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia; implications for the mapping of the BOR gene

CHARGE syndrome: Report of 47 cases and review

Short-term treatment by implantable pump does not impair lipoprotein pattern in IDDM patients

Hemoglobin Saverne: A New Variant with Elongated β Chains: Structural and Functional Properties

HB J-Cordoba [α2Aβ2 95 (FG2)LYS →MET] A New HB Variant Found in Argentina

Long segment and short segment familial Hirschprung's disease : variable clinical expression at the RET locus

Aktive Filter

Suchergebnisse filtern