![]() | Jörg WiltingDepartment of Anatomy and Cell Biology, University Medical School Göttingen, Göttingen, Germany | Zentrum für Anatomie, Universitätsmedizin Göttingen, Göttingen, Deutschland | ... |
KOL Resume for Jörg Wilting
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2021 | Department of Anatomy and Cell Biology, University Medical School Göttingen, Göttingen, Germany Zentrum für Anatomie, Universitätsmedizin Göttingen, Göttingen, Deutschland |
2020 | Institute of Anatomy and Cell Biology, University Medical Centre Göttingen, Germany |
2019 | Institute of Anatomy and Cell Biology, School of Medicine, Georg-August-Universität Gőttingen, Gőttingen, Germany |
2018 | Institute for Anatomy and Cell Biology, University Medical Hospital Göttingen, Kreuzbergring 36, D-37075, Göttingen, Germany |
2017 | Institute of Anatomy and Cell Biology, University Medical Center, D-37075 Goettingen, Germany |
2016 | Department of Anatomy and Cell Biology, University Medical Centre of the Georg-August University of Göttingen, Göttingen, Germany |
2015 | Institute of Anatomy and Cell Biology, University Medical School Goettingen, Kreuzbergring 36, 37075, Goettingen, Germany |
2014 | Department of Anatomy and Cell Biology, University Medical Center Goettingen, Kreuzbergring 36, Goettingen 37075, Germany |
2013 | Department of Anatomy and Cell Biology, University Medicine Gottingen, Kreuzbergring 36, 37075, Goettingen, Germany |
2012 | Center of Anatomy, Department of Anatomy and Cell Biology; Department of Anatomy and Cell Biology, University Medicine Goettingen, 37075 Goettingen, Germany |
2011 | Department Anatomy and Cell Biology, Georg-August-University, Goettingen, Germany |
2010 | Center of Anatomy, Department of Anatomy and Cell Biology, University Medicine Goettingen, Goettingen, Germany. Department of Anatomy and Cell Biology, Georg-August-University, Goettingen, Germany |
2009 | Abteilung Anatomie und Zellbiologie, Zentrum Anatomie, Universitätsmedizin Göttingen, Göttingen, Germany |
2008 | University Medicine Goettingen, Centre of Anatomy, Department of Anatomy and Cell Biology, Kreuzbergring 36, 37075 Goettingen, Germany |
2007 | Department of Anatomy and Cell Biology, Georg‐August‐University, Goettingen, Germany |
2006 | Children's Hospital, Pediatrics I, University of Goettingen, Goettingen, Germany |
2005 | Children's Hospital, Pediatrics I, University of Goettingen, Robert-Koch-Strasse 40, 37075 Göttingen, Germany. Max-Planck Institut für Neurobiologie [S.D., R.B., G.A.W., R.K.], D-82152 Martinsried, Germany; Abt. Pädiatrie I [S.D., J.W., L.S.], Zentrum für Kinderheilkunde und Jugendmedizin, Bereich Humanmedizin der Universität Göttingen, D-37075 Göttingen, Germany; and Zentrum für Gefässmedizin [D.A.L.], D-22761 Hamburg, Germany |
2004 | Children's Hospital, Pediatrics I, Göttingen, Germany. Abt. Pädiatrie I, Zentrum für Kinderheilkunde und Jugendmedizin, Klinikum der Georg-August-Universität Göttingen, Germany |
2003 | Children's Hospital, University of Goettingen, Robert-Koch-Strasse 40, 37075, Goettingen, Germany |
2002 | Anatomisches Institut der Albert‐Ludwigs‐Universität Freiburg, Albertstrasse 17, 79104, Freiburg, Germany |
2001 | Anatomisches Institut II der Albert-Ludwigs-Universität Freiburg, Albertstrasse 17, 79104, Freiburg, Germany |
2000 | Institute of Anatomy, University of Freiburg, P.O. Box 111, D-79001, Freiburg, Germany e-mail: Tel.: 761-203-5088, Fax: 761-203-5091, DE Anatomisches Institut der Albert-Ludwigs-Universität, Freiburg, Germany. |
1999 | Anatomisches Institut der Albert-Ludwigs Universität Freiburg, Albertstrasse 17, D-79104 Freiburg, Germany e-mail: Tel.: +49 761/203 5087; Fax: +49 761/203 5091, DE |
1998 | Institute of Anatomy II, University of Freiburg, Albertstrasse 17, D-79104, Freiburg, Germany |
1997 | Anatomisches Institut der Universität Freiburg, Albertstrasse 17, D-79104 Freiburg, Germany Tel.: 0761/203-5088; Fax: 0761/203-5091; e-mail: DE |
1996 | Fachbereich Mathematik & Naturwissenschaften der Fachhochschule Darmstadt, Schoefferstr 3, Darmstadt, Germany Anatomisches Institut, Lehrstuhl II, Albert-Ludwigs-Universität Freiburg, Albertstrasse 17, D-79104, Freiburg |
1995 | Anatomisches Institut, Freiburg, Germany. Department of Anatomy, University Freiburg, Germany |
1994 | Department of Developmental Biology, Max-Planck Institute of Immunobiology, Freiburg, FRG. Anatomisches Institut der Albert-Ludwigs-Universität Freiburg, Albertstrasse 17, D-79104, Freiburg i.Br., Germany |
1993 | Anatomisches Institut II und, Institut für Molekulare Zellbiologie der Albert-Ludwigs-Universität, Freiburg, BRD Department of Developmental Biology, Max-Planck-Institute of Immunobiology, Freiburg, Germany |
Jörg Wilting: Influence Statistics
Concept | World rank |
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lateral posterior expansions | #1 |
human lymphatic collectors | #1 |
sympathoadrenal children | #1 |
reifung vegfc | #1 |
metabolites lymphatics | #1 |
lymphendothelial characteristics | #1 |
wellknown lec markers | #1 |
funktion lymphgefäße | #1 |
human numerous receptors | #1 |
placenta lyve1 | #1 |
crl lung surface | #1 |
aktivierung vegfr3 signaltransduktionskaskaden | #1 |
immune surveillance outline | #1 |
embryonic lymph | #1 |
pax1 expressing | #1 |
markers lecs | #1 |
application wnt | #1 |
lymphatic plexus | #1 |
knowledge essential steps | #1 |
reelin lrp8 | #1 |
entscheidender weise genetik | #1 |
lymphogenic dissemination | #1 |
pulmonary pleura | #1 |
screeningverfahren wissen | #1 |
lu muscle fibers | #1 |
authentic chp100 | #1 |
genetik entwicklung | #1 |
lymphatics wnt5a | #1 |
tendon collagen bundle | #1 |
thigh vimentin | #1 |
lymphangiogenesis inhibitor | #1 |
largest collectors | #1 |
imr32 chp100 | #1 |
tumor lymphangiogenesis lec | #1 |
selected cases specific | #1 |
s9 lungs | #1 |
cd31 prox1 | #1 |
tumors chick | #1 |
equal immunostaining | #1 |
weise beitrag | #1 |
extension lymphangiogenesis | #1 |
prominent nb cell | #1 |
210290 mm | #1 |
lecs fibrosis | #1 |
wnt5a − | #1 |
lateral lungs | #1 |
vascular embryology | #1 |
signaling sympathoadrenal | #1 |
schritte signaltransduktionskaskaden | #1 |
Open the FULL List in Excel | |
Prominent publications by Jörg Wilting
Pax1 and Pax9 represent a subfamily of paired-box-containing genes. In vertebrates, Pax1 and Pax9 transcripts have been found specifically in mesodermal tissues and the pharyngeal endoderm. Pax1 expression in the sclerotomes has been shown to be indispensable for proper formation of the axial skeleton, but expression of Pax1 in the endoderm has not been studied in detail. We have cloned the chick homologue of the murine Pax9 gene. Our results show that transcripts of Pax1 and Pax9 are ...
Known for Pax1 Pax9 | Paraxial Mesoderm | Pharyngeal Endoderm | Transcription Factors | Axial Skeleton |
We have studied the effect of VEGF(121) homodimer and VEGF(121/165) heterodimer on the chorioallantoic membrane (CAM) of 13-day-old chick embryos. The factors were applied in doses of 2-4 micrograms and the effects were evaluated macroscopically after 2 and 3 days. Histological studies were performed on semi- and ultrathin sections. Proliferation was studied according to the BrdU-anti-BrdU method on whole mounts and sections. The labeling density was quantified in whole mounts. The ...
Known for Vascular Endothelial | Lymphatic Vessels | Chorioallantoic Membrane | Fractal Dimension | Vegf121 165 |
VEGF and VEGF-C: Specific Induction of Angiogenesis and Lymphangiogenesis in the Differentiated Avian Chorioallantoic Membrane
[ PUBLICATION ]
The lymphangiogenic potency of endothelial growth factors has not been studied to date. This is partially due to the lack of in vivo lymphangiogenesis assays. We have studied the lymphatics of differentiated avian chorioallantoic membrane (CAM) using microinjection of Mercox resin, semi- and ultrathin sectioning, immunohistochemical detection of fibronectin and alpha-smooth muscle actin, and in situ hybridization with VEGFR-2 and VEGFR-3 probes. CAM is drained by lymphatic vessels which ...
Known for Factor Vascular | Endothelial Growth | Chorioallantoic Membrane | Vegf Vegfc | Situ Hybridization |
The transcription factor Prox1 is a marker for lymphatic endothelial cells in normal and diseased human tissues
[ PUBLICATION ]
Detection of lymphatic endothelal cells (LECs) has been problematic because of the lack of specific markers. The homeobox transcription factor Prox1 is expressed in LECs of murine and avian embryos. We have studied expression of Prox1 in human tissues with immunofluorescence. In 19-wk-old human fetuses, Prox1 and vascular endothelial growth factor receptor-3 (VEGFR-3) are coexpressed in LECs of lymphatic trunks and lymphatic capillaries. Prox1 is located in the nucleus, and its ...
Known for Lymphatic Endothelial | Factor Prox1 | Vegfr3 Cd31 | Human Tissues | Lecs Becs |
Mouse lung contains endothelial progenitors with high capacity to form blood and lymphatic vessels
[ PUBLICATION ]
BACKGROUND: Postnatal endothelial progenitor cells (EPCs) have been successfully isolated from whole bone marrow, blood and the walls of conduit vessels. They can, therefore, be classified into circulating and resident progenitor cells. The differentiation capacity of resident lung endothelial progenitor cells from mouse has not been evaluated.
RESULTS: In an attempt to isolate differentiated mature endothelial cells from mouse lung we found that the lung contains EPCs with a high ...
Known for Lymphatic Vessels | Endothelial Progenitor | Mouse Lung | Inbred C57bl Neovascularization | Stem Cells |
Pax-1, a regulator of sclerotome development is induced by notochord and floor plate signals in avian embryos
[ PUBLICATION ]
Pax-1 encodes for a DNA-binding transcriptional activator that was originally discovered in murine embryos using a probe from the Drosophila paired-box-containing gene, gooseberry-distal. We have cloned the avian Pax-1 gene as a basis for experimental studies of the induction of Pax-1 in the paraxial mesoderm. The amino acid sequence of the paired-domain is exactly the same in the quail and mouse, whereas outside the paired-domain there is 61% homology. Starting at about the eight-somite ...
Known for Avian Embryos | Paraxial Mesoderm | Sclerotome Development | Pax1 Cells | Floor Plate |
Neuroblastoma Progression Correlates with Downregulation of the Lymphangiogenesis Inhibitor sVEGFR-2
[ PUBLICATION ]
PURPOSE: Tumor progression correlates with the induction of a dense supply of blood vessels and the formation of peritumoral lymphatics. Hemangiogenesis and lymphangiogenesis are potently regulated by members of the vascular endothelial growth factor (VEGF) family. Previous studies have indicated the upregulation of VEGF-A and -C in progressed neuroblastoma, however, quantification was performed using semiquantitative methods, or patients who had received radiotherapy or chemotherapy ...
Known for Vascular Endothelial | Growth Factor | Neuroblastoma Progression | Vegf Receptors | Blood Vessels |
Vascular endothelial growth factor (VEGF) and placenta growth factor (PIGF) are members of a dimeric-growth-factor family with angiogenic properties. VEGF is a highly potent and specific mitogen for endothelial cells, playing a vital role in angiogenesis in vivo. The role of PIGF is less clear. We expressed the monomeric splice forms VEGF-165, VEGF-121, PIGF-1 and PIGF-2 as unfused genes in Escherichia coli using the pCYTEXP expression system. In vitro dimerization experiments revealed ...
Known for Endothelial Growth | Factor Vascular | Pregnancy Proteins | Mitogenic Activity | Vegf Placenta |
Synthesis and assembly of functionally active human vascular endothelial growth factor homodimers in insect cells
[ PUBLICATION ]
Vascular endothelial growth factor (VEGF) is an angiogenic growth factor with a target-cell specificity highly restricted to vascular endothelial cells. Recombinant baculovirus were constructed for the production of two different forms of the human VEGF protein in insect cells. VEGF165 and VEGF121 proteins produced by Sf158 cells underwent a similar processing compared with mammalian cells, including efficient glycosylation, formation of a disulfide-linked dimer and secretion into the ...
Known for Vascular Endothelial | Insect Cells | Growth Factor | Cultured Chromatography | Biological Activity |
Altered Expression Patterns of EphrinB2 and EphB2 in Human Umbilical Vessels and Congenital Venous Malformations
[ PUBLICATION ]
Vascular malformations cause discomfort and pain in children and are often associated with skeletal hypertrophy. Their molecular basis is poorly understood. Ephrin ligands and Eph receptor tyrosine kinases are involved in embryonic vascular development. In mice, some ephrin/Eph family members show a complementary expression pattern in blood vessels, with ephrinB2 being expressed on arterial and EphB4 on venous endothelium. Targeted deletions of the genes reveal their essential roles for ...
Known for Venous Malformations | Ephrinb2 Ephb4 | Ephb2 Receptor | Human Umbilical | Blood Vessels |
Scatter Factor/Hepatocyte Growth Factor (SF/HGF) Induces Emigration of Myogenic Cells at Interlimb Levelin Vivo
[ PUBLICATION ]
The initiating event in the migration of myogenic cells to the limb buds is an epitheliomesenchymal transformation of cells located at the lateral edge of the dermomyotome. Recently, a targeted mutation of c-met in mice demonstrated an essential role of this tyrosine kinase receptor and its ligand, scatter factor/hepatocyte growth factor (SF/HGF), in the migration of myogenic cells to the limb buds. Here, we show that ectopic application of exogenous SF/HGF induces emigration of ...
Known for Myogenic Cells | Growth Factor | Limb Buds | Hgf Migration | Lateral Edge |
Key People For Endothelial Cells
Jörg Wilting:Expert Impact
Concepts for whichJörg Wiltinghas direct influence:Endothelial cells, Lymphatic vessels, Vascular endothelial, Somitocoele cells, Growth factor, Avian embryos, Endothelial growth, Chick embryos.
Jörg Wilting:KOL impact
Concepts related to the work of other authors for whichfor which Jörg Wilting has influence:Growth factor, Endothelial cells, Lymphatic vessels, Neural tube, Gene expression, Chick embryo, Skeletal muscle.
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