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...

Secreted cathepsin L generates endostatin from collagen XVIII

The EMBO journal, 2000-03, Vol.19 (6), p.1187-1194

2000

Volltextzugriff (PDF)

Genetics of cerebral cavernous malformations (CCM)

Deutsche medizinische Wochenschrift (1946), 2007-09, Vol.132 (38), p.1967

Felbor, U

2007

Volltextzugriff (PDF)

Long-term outcome and quality of life after Cavernoma resection: Eloquent vs. Non-Eloquent areas

Brain & spine, 2021, Vol.1, p.100357, Article 100357

2021

Volltextzugriff (PDF)

Highly variable intrafamilial manifestations of a CCM3 mutation ranging from acute childhood cerebral haemorrhage to late-onset meningiomas

Clinical neurology and neurosurgery, 2015-01, Vol.128, p.41-43

2015

Volltextzugriff (PDF)

35 Jahre Greifswalder Institut für Humangenetik

Medizinische Genetik, 2014-06, Vol.26 (2), p.278-280

Felbor, U.

2014

Volltextzugriff (PDF)

35 Jahre Greifswalder Institut für Humangenetik: 35th anniversary of the Greifswald Institute for Human Genetics

Medizinische Genetik, 2014, Vol.26 (2), p.278-280

Felbor, U.

2014

Volltextzugriff (PDF)

Congenital macrothrombocytopenia associated with a combination of functional polymorphisms in the TUBB1 gene

Hämostaseologie, 2015, Vol.35 Suppl 1 (S 01), p.S18-S21

2015

Volltextzugriff (PDF)

Large deletions play a minor but essential role in congenital coagulation factor VII and X deficiencies

Hämostaseologie, 2015-01, Vol.35 Suppl 1 (S 01), p.S36-S42

2015

Volltextzugriff (PDF)

Endosomal Proteolysis of the Ebola Virus Glycoprotein Is Necessary for Infection

Science (American Association for the Advancement of Science), 2005-06, Vol.308 (5728), p.1643-1645

2005

Volltextzugriff (PDF)

Severe FX deficiency caused by a previously unidentified 4-bp deletion compound heterozygous with a large deletion involving FVII and FX genes

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-03, Vol.18 (2), p.e55-e58

2012

Volltextzugriff (PDF)

35 Jahre Greifswalder Institut für Humangenetik: 35th anniversary of the Greifswald Institute for Human Genetics

Medizinische Genetik, 2014-06, Vol.26 (2), p.278-280

Felbor, U.

2014

Volltextzugriff (PDF)

Genetik zerebraler kavernöser Gefäßmalformationen

Deutsche medizinische Wochenschrift, 2007-09, Vol.132 (38), p.1967-1970

Felbor, U

2007

Volltextzugriff (PDF)

Large germline deletions and duplication in isolated cerebral cavernous malformation patients

Neurogenetics, 2007-04, Vol.8 (2), p.149-153

2007

Volltextzugriff (PDF)

The rare human fragile site 16B

Cytogenetic and Genome Research, 2003-01, Vol.100 (1-4), p.85-88

2003

Volltextzugriff (PDF)

Neuronal Loss and Brain Atrophy in Mice Lacking Cathepsins B and L

Proceedings of the National Academy of Sciences - PNAS, 2002-06, Vol.99 (12), p.7883-7888

2002

Volltextzugriff (PDF)

Generation and degradation of human endostatin proteins by various proteinases

FEBS letters, 2000-12, Vol.486 (3), p.247-251

2000

Volltextzugriff (PDF)

A novel Ser156Cys mutation in the tissue inhibitor of metalloproteinases-3 (TIMP3) in Sorsby's fundus dystrophy with unusual clinical features

Human molecular genetics, 1995-12, Vol.4 (12), p.2415-2416

1995

Volltextzugriff (PDF)

Sensitization to the lysosomal cell death pathway upon immortalization and transformation

Cancer research (Chicago, Ill.), 2004-08, Vol.64 (15), p.5301-5310

2004

Volltextzugriff (PDF)

Das Institut für Vererbungswissenschaft und Rasseforschung der Universität Würzburg 1937-1945

Wurzburger medizinhistorische Mitteilungen, 1993, Vol.11, p.155

Felbor, U

1993

Volltextzugriff (PDF)

A second independent Tyr168Cys mutation in the tissue inhibitor of metalloproteinases-3 (TIMP3) in Sorsby's fundus dystrophy

Journal of medical genetics, 1996-03, Vol.33 (3), p.233-236

1996

Volltextzugriff (PDF)

Ocular ochronosis in alkaptonuria patients carrying mutations in the homogentisate 1,2-dioxygenase gene

British journal of ophthalmology, 1999-06, Vol.83 (6), p.680-683

1999

Volltextzugriff (PDF)

Mosaicism for an ectopic NOR at 8pter and a complex rearrangement of chromosome 8 in a patient with severe psychomotor retardation

Cytogenetic and genome research, 2004-01, Vol.106 (1), p.55-60

2004

Volltextzugriff (PDF)

Genomic organization and chromosomal localization of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene: a candidate for 6q-linked retinopathies

Cytogenetic and genome research, 1998, Vol.81 (1), p.12-17

1998

Volltextzugriff (PDF)

A Nonsense Mutation in MSX1 Causes Witkop Syndrome

American journal of human genetics, 2001-07, Vol.69 (1), p.67-74

2001

Volltextzugriff (PDF)

Highly variable intrafamilial manifestations of aCCM3mutation ranging from acute childhood cerebral haemorrhage to late-onset meningiomas

Clinical neurology and neurosurgery, 2015-01, Vol.128, p.41

2015

Volltextzugriff (PDF)

1 – 25 von 49

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(40)
Mit Volltextzugriff
(39)

Publikationsform

Sprache

Englisch
(38)
Deutsch
(14)
Japanisch
(8)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Secreted cathepsin L generates endostatin from collagen XVIII

Genetics of cerebral cavernous malformations (CCM)

Long-term outcome and quality of life after Cavernoma resection: Eloquent vs. Non-Eloquent areas

Highly variable intrafamilial manifestations of a CCM3 mutation ranging from acute childhood cerebral haemorrhage to late-onset meningiomas

35 Jahre Greifswalder Institut für Humangenetik

35 Jahre Greifswalder Institut für Humangenetik: 35th anniversary of the Greifswald Institute for Human Genetics

Congenital macrothrombocytopenia associated with a combination of functional polymorphisms in the TUBB1 gene

Large deletions play a minor but essential role in congenital coagulation factor VII and X deficiencies

Endosomal Proteolysis of the Ebola Virus Glycoprotein Is Necessary for Infection

Severe FX deficiency caused by a previously unidentified 4-bp deletion compound heterozygous with a large deletion involving FVII and FX genes

35 Jahre Greifswalder Institut für Humangenetik: 35th anniversary of the Greifswald Institute for Human Genetics

Genetik zerebraler kavernöser Gefäßmalformationen

Large germline deletions and duplication in isolated cerebral cavernous malformation patients

The rare human fragile site 16B

Neuronal Loss and Brain Atrophy in Mice Lacking Cathepsins B and L

Generation and degradation of human endostatin proteins by various proteinases

A novel Ser156Cys mutation in the tissue inhibitor of metalloproteinases-3 (TIMP3) in Sorsby's fundus dystrophy with unusual clinical features

Sensitization to the lysosomal cell death pathway upon immortalization and transformation

Das Institut für Vererbungswissenschaft und Rasseforschung der Universität Würzburg 1937-1945

A second independent Tyr168Cys mutation in the tissue inhibitor of metalloproteinases-3 (TIMP3) in Sorsby's fundus dystrophy

Ocular ochronosis in alkaptonuria patients carrying mutations in the homogentisate 1,2-dioxygenase gene

Mosaicism for an ectopic NOR at 8pter and a complex rearrangement of chromosome 8 in a patient with severe psychomotor retardation

Genomic organization and chromosomal localization of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene: a candidate for 6q-linked retinopathies

A Nonsense Mutation in MSX1 Causes Witkop Syndrome

Highly variable intrafamilial manifestations of aCCM3mutation ranging from acute childhood cerebral haemorrhage to late-onset meningiomas

Suchergebnisse filtern