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...

Transcriptional control of chondrocyte fate and differentiation

Birth defects research. Part C. Embryo today, 2005-09, Vol.75 (3), p.200-212

2005

Volltextzugriff (PDF)

Endothelial MAP2K1 mutations in arteriovenous malformation activate the RAS/MAPK pathway

Biochemical and biophysical research communications, 2020-08, Vol.529 (2), p.450-454

2020

Volltextzugriff (PDF)

Arteriovenous malformation Map2k1 mutation affects vasculogenesis

Scientific reports, 2023-07, Vol.13 (1), p.11074-11074, Article 11074

2023

Volltextzugriff (PDF)

Arteriovenous Malformation MAP2K1 Mutation Causes Local Cartilage Overgrowth by a Cell-Non Autonomous Mechanism

Scientific reports, 2020-03, Vol.10 (1), p.4428-4428, Article 4428

2020

Volltextzugriff (PDF)

Arteriovenous malformation associated with a HRAS mutation

Human genetics, 2019-12, Vol.138 (11-12), p.1419-1421

2019

Volltextzugriff (PDF)

Endothelial cell expression of mutant Map2k1 causes vascular malformations in mice

Angiogenesis (London), 2023-02, Vol.26 (1), p.97-105

2023

Volltextzugriff (PDF)

The secreted glycoprotein lubricin protects cartilage surfaces and inhibits synovial cell overgrowth

The Journal of clinical investigation, 2005-03, Vol.115 (3), p.622-631

2005

Volltextzugriff (PDF)

Arteriovenous malformation phenotype resembling congenital hemangioma contains KRAS mutations

Clinical genetics, 2020-12, Vol.98 (6), p.595-597

2020

Volltextzugriff (PDF)

Intramuscular fast-flow vascular anomaly contains somatic MAP2K1 and KRAS mutations

Angiogenesis (London), 2019-11, Vol.22 (4), p.547-552

2019

Volltextzugriff (PDF)

The skeletal phenotype of achondrogenesis type 1A is caused exclusively by cartilage defects

Development (Cambridge), 2018-01, Vol.145 (1), p.dev156588-dev156588

2018

Volltextzugriff (PDF)

Large-scale real-life implementation of technology-enabled care to maximize hospitals' medical surge preparedness during future infectious disease outbreaks and winter seasons: a viewpoint

Frontiers in public health, 2023-08, Vol.11, p.1149247-1149247

2023

Volltextzugriff (PDF)

Lipoblastoma phenotype contains a somatic PIK3CA mutation

Pediatric dermatology, 2021-01, Vol.38 (1), p.299-300

2021

Volltextzugriff (PDF)

Sox5 and Sox6 are required for notochord extracellular matrix sheath formation, notochord cell survival and development of the nucleus pulposus of intervertebral discs

Development (Cambridge), 2003-03, Vol.130 (6), p.1135-1148

2003

Volltextzugriff (PDF)

The Transcription Factors L-Sox5 and Sox6 Are Essential for Cartilage Formation

Developmental cell, 2001-08, Vol.1 (2), p.277-290

2001

Volltextzugriff (PDF)

Historical contingency shapes adaptive radiation in Antarctic fishes

Nature ecology & evolution, 2019-07, Vol.3 (7), p.1102-1109

2019

Volltextzugriff (PDF)

Lubricin Restoration in a Mouse Model of Congenital Deficiency

Arthritis & rheumatology (Hoboken, N.J.), 2015-11, Vol.67 (11), p.3070-3081

2015

Volltextzugriff (PDF)

Notch3 in Human Breast Cancer Cell Lines Regulates Osteoblast-Cancer Cell Interactions and Osteolytic Bone Metastasis

The American journal of pathology, 2010-09, Vol.177 (3), p.1459-1469

2010

Volltextzugriff (PDF)

Sox5 and Sox6 Are Needed to Develop and Maintain Source, Columnar, and Hypertrophic Chondrocytes in the Cartilage Growth Plate

The Journal of cell biology, 2004-03, Vol.164 (5), p.747-758

2004

Volltextzugriff (PDF)

P30. Arteriovenous Malformation Map2k1-mutant Endothelial Cells Exhibit Dysregulated Vasculogenesis In-vitro and In-vivo

Plastic and reconstructive surgery. Global open, 2024-05, Vol.12 (S5), p.53-53

2024

Volltextzugriff (PDF)

79. Arteriovenous Malformation MAP2K1-mutant Endothelial Cells Exhibit Dysregulated Vasculogenesis In-vitro And In-vivo

Plastic and reconstructive surgery. Global open, 2024-04, Vol.12 (S4), p.53-53

2024

Volltextzugriff (PDF)

Bockenheimer disease is associated with a TEK variant

Cold Spring Harbor molecular case studies, 2021-12, Vol.7 (6), p.a006119

2021

Volltextzugriff (PDF)

Parkes Weber syndrome with lymphedema caused by a somatic KRAS variant

Cold Spring Harbor molecular case studies, 2021-12, Vol.7 (6), p.a006118

2021

Volltextzugriff (PDF)

96. Activating MAP2K1 Mutation in Zebrafish Endothelial Cells Causes Arteriovenous Shunts

Plastic and reconstructive surgery. Global open, 2022-06, Vol.10 (6S), p.63-63

2022

Volltextzugriff (PDF)

75. Trametinib Prevents Formation of Vascular Lesions in a MAP2k1-p.K57N Arteriovenous Malformation Mouse Model

Plastic and reconstructive surgery. Global open, 2024-04, Vol.12 (S4), p.50-51

2024

Volltextzugriff (PDF)

147. MAP2K1 Mutant Murine Model Recapitulates Human Cutaneous Arteriovenous Malformation

Plastic and reconstructive surgery. Global open, 2023-05, Vol.11 (5S), p.92-92

2023

Volltextzugriff (PDF)

1 – 25 von 429

Suche als RSS-Feed

Aktive Filter

ThemaMale

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(381)
Mit Volltextzugriff
(382)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(205)
Life Sciences & Biomedicine
(174)
Humans
(101)
Animals
(50)
Oncology
(40)
Cardiology
(39)
Cardiovascular System & Cardiology
(35)
Cardiovascular
(33)
Cardiac & Cardiovascular Systems
(31)
Stents
(29)
Clinical Trials
(27)
Mice
(27)
Patients
(27)
Immunotherapy
(24)
Internal Medicine
(23)
Biological And Medical Sciences
(22)
Mutation
(22)
Cell Biology
(20)
Treatment Outcome
(20)
Science & Technology - Other Topics
(19)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(2)
... seit 90 Tagen
(5)

Menü

Weitere Dienste

Einstellungen

Transcriptional control of chondrocyte fate and differentiation

Endothelial MAP2K1 mutations in arteriovenous malformation activate the RAS/MAPK pathway

Arteriovenous malformation Map2k1 mutation affects vasculogenesis

Arteriovenous Malformation MAP2K1 Mutation Causes Local Cartilage Overgrowth by a Cell-Non Autonomous Mechanism

Arteriovenous malformation associated with a HRAS mutation

Endothelial cell expression of mutant Map2k1 causes vascular malformations in mice

The secreted glycoprotein lubricin protects cartilage surfaces and inhibits synovial cell overgrowth

Arteriovenous malformation phenotype resembling congenital hemangioma contains KRAS mutations

Intramuscular fast-flow vascular anomaly contains somatic MAP2K1 and KRAS mutations

The skeletal phenotype of achondrogenesis type 1A is caused exclusively by cartilage defects

Large-scale real-life implementation of technology-enabled care to maximize hospitals' medical surge preparedness during future infectious disease outbreaks and winter seasons: a viewpoint

Lipoblastoma phenotype contains a somatic PIK3CA mutation

Sox5 and Sox6 are required for notochord extracellular matrix sheath formation, notochord cell survival and development of the nucleus pulposus of intervertebral discs

The Transcription Factors L-Sox5 and Sox6 Are Essential for Cartilage Formation

Historical contingency shapes adaptive radiation in Antarctic fishes

Lubricin Restoration in a Mouse Model of Congenital Deficiency

Notch3 in Human Breast Cancer Cell Lines Regulates Osteoblast-Cancer Cell Interactions and Osteolytic Bone Metastasis

Sox5 and Sox6 Are Needed to Develop and Maintain Source, Columnar, and Hypertrophic Chondrocytes in the Cartilage Growth Plate

P30. Arteriovenous Malformation Map2k1-mutant Endothelial Cells Exhibit Dysregulated Vasculogenesis In-vitro and In-vivo

79. Arteriovenous Malformation MAP2K1-mutant Endothelial Cells Exhibit Dysregulated Vasculogenesis In-vitro And In-vivo

Bockenheimer disease is associated with a TEK variant

Parkes Weber syndrome with lymphedema caused by a somatic KRAS variant

96. Activating MAP2K1 Mutation in Zebrafish Endothelial Cells Causes Arteriovenous Shunts

75. Trametinib Prevents Formation of Vascular Lesions in a MAP2k1-p.K57N Arteriovenous Malformation Mouse Model

147. MAP2K1 Mutant Murine Model Recapitulates Human Cutaneous Arteriovenous Malformation

Aktive Filter

Suchergebnisse filtern