Search Results - (Author, Cooperation:U. Lang)
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1J. George ; J. S. Lim ; S. J. Jang ; Y. Cun ; L. Ozretic ; G. Kong ; F. Leenders ; X. Lu ; L. Fernandez-Cuesta ; G. Bosco ; C. Muller ; I. Dahmen ; N. S. Jahchan ; K. S. Park ; D. Yang ; A. N. Karnezis ; D. Vaka ; A. Torres ; M. S. Wang ; J. O. Korbel ; R. Menon ; S. M. Chun ; D. Kim ; M. Wilkerson ; N. Hayes ; D. Engelmann ; B. Putzer ; M. Bos ; S. Michels ; I. Vlasic ; D. Seidel ; B. Pinther ; P. Schaub ; C. Becker ; J. Altmuller ; J. Yokota ; T. Kohno ; R. Iwakawa ; K. Tsuta ; M. Noguchi ; T. Muley ; H. Hoffmann ; P. A. Schnabel ; I. Petersen ; Y. Chen ; A. Soltermann ; V. Tischler ; C. M. Choi ; Y. H. Kim ; P. P. Massion ; Y. Zou ; D. Jovanovic ; M. Kontic ; G. M. Wright ; P. A. Russell ; B. Solomon ; I. Koch ; M. Lindner ; L. A. Muscarella ; A. la Torre ; J. K. Field ; M. Jakopovic ; J. Knezevic ; E. Castanos-Velez ; L. Roz ; U. Pastorino ; O. T. Brustugun ; M. Lund-Iversen ; E. Thunnissen ; J. Kohler ; M. Schuler ; J. Botling ; M. Sandelin ; M. Sanchez-Cespedes ; H. B. Salvesen ; V. Achter ; U. Lang ; M. Bogus ; P. M. Schneider ; T. Zander ; S. Ansen ; M. Hallek ; J. Wolf ; M. Vingron ; Y. Yatabe ; W. D. Travis ; P. Nurnberg ; C. Reinhardt ; S. Perner ; L. Heukamp ; R. Buttner ; S. A. Haas ; E. Brambilla ; M. Peifer ; J. Sage ; R. K. Thomas
Nature Publishing Group (NPG)
Published 2015Staff ViewPublication Date: 2015-07-15Publisher: Nature Publishing Group (NPG)Print ISSN: 0028-0836Electronic ISSN: 1476-4687Topics: BiologyChemistry and PharmacologyMedicineNatural Sciences in GeneralPhysicsPublished by: -
2M. Peifer ; F. Hertwig ; F. Roels ; D. Dreidax ; M. Gartlgruber ; R. Menon ; A. Kramer ; J. L. Roncaioli ; F. Sand ; J. M. Heuckmann ; F. Ikram ; R. Schmidt ; S. Ackermann ; A. Engesser ; Y. Kahlert ; W. Vogel ; J. Altmuller ; P. Nurnberg ; J. Thierry-Mieg ; D. Thierry-Mieg ; A. Mariappan ; S. Heynck ; E. Mariotti ; K. O. Henrich ; C. Gloeckner ; G. Bosco ; I. Leuschner ; M. R. Schweiger ; L. Savelyeva ; S. C. Watkins ; C. Shao ; E. Bell ; T. Hofer ; V. Achter ; U. Lang ; J. Theissen ; R. Volland ; M. Saadati ; A. Eggert ; B. de Wilde ; F. Berthold ; Z. Peng ; C. Zhao ; L. Shi ; M. Ortmann ; R. Buttner ; S. Perner ; B. Hero ; A. Schramm ; J. H. Schulte ; C. Herrmann ; R. J. O'Sullivan ; F. Westermann ; R. K. Thomas ; M. Fischer
Nature Publishing Group (NPG)
Published 2015Staff ViewPublication Date: 2015-10-16Publisher: Nature Publishing Group (NPG)Print ISSN: 0028-0836Electronic ISSN: 1476-4687Topics: BiologyChemistry and PharmacologyMedicineNatural Sciences in GeneralPhysicsPublished by: -
3Staff View
Publication Date: 2018-12-07Publisher: American Association for the Advancement of Science (AAAS)Print ISSN: 0036-8075Electronic ISSN: 1095-9203Topics: BiologyChemistry and PharmacologyGeosciencesComputer ScienceMedicineNatural Sciences in GeneralPhysicsKeywords: Medicine, DiseasesPublished by: -
4Winiger, B.P. ; Birabeau, M.A. ; Lang, U. ; Capponi, A.M. ; Sizonenko, P.C. ; Aubert, M.L.
Amsterdam : ElsevierStaff ViewISSN: 0303-7207Keywords: CHAPS ; GnRH ; GnRH receptor ; Triton ; membrane proteinSource: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002Topics: BiologyMedicineType of Medium: Electronic ResourceURL: -
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ISSN: 0368-1874Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002Topics: Chemistry and PharmacologyType of Medium: Electronic ResourceURL: -
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ISSN: 0014-5793Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002Topics: BiologyChemistry and PharmacologyPhysicsType of Medium: Electronic ResourceURL: -
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ISSN: 0014-5793Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002Topics: BiologyChemistry and PharmacologyPhysicsType of Medium: Electronic ResourceURL: -
8Staff View
ISSN: 0022-2828Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002Topics: MedicineType of Medium: Electronic ResourceURL: -
9Staff View
ISSN: 0022-2828Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002Topics: MedicineType of Medium: Electronic ResourceURL: -
10Staff View
ISSN: 0022-0728Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002Topics: Chemistry and PharmacologyType of Medium: Electronic ResourceURL: -
11Geiger, H. ; Lang, U. ; Britsch, E. ; Mabry, T.J. ; Suhr-Schucker, U. ; Velde, G.V. ; Waldrum, H.
Amsterdam : ElsevierStaff ViewISSN: 0031-9422Keywords: Equisetaceae ; Equisetum telmateja ; acetylated kaempferol glycosides. ; kaempferol glycosidesSource: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002Topics: BiologyChemistry and PharmacologyType of Medium: Electronic ResourceURL: -
12Staff View
ISSN: 0022-4731Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002Topics: BiologyChemistry and PharmacologyType of Medium: Electronic ResourceURL: -
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ISSN: 1420-8970Source: Springer Online Journal Archives 1860-2000Topics: MathematicsNotes: Abstract. We generalize Kirszbraun's extension theorem for Lipschitz maps between (subsets of) euclidean spaces to metric spaces with upper or lower curvature bounds in the sense of A.D. Alexandrov. As a by-product we develop new tools in the theory of tangent cones of these spaces and obtain new characterization results which may be of independent interest.Type of Medium: Electronic ResourceURL: -
14Staff View
ISSN: 1420-8970Source: Springer Online Journal Archives 1860-2000Topics: MathematicsNotes: Abstract. We prove that every $ \lambda $ -Lipschitz map $ f : S \to Y $ defined on a subset of an arbitrary metric space X possesses a $ c \lambda $ -Lipschitz extension $ \bar{f} : X \to Y $ for some $ c = c(Y) \ge 1 $ provided Y is a Hadamard manifold which satisfies one of the following conditions: (i) Y has pinched negative sectional curvature, (ii) Y is homogeneous, (iii) Y is two-dimensional. In case (i) the constant c depends only on the dimension of Y and the pinching constant, in case (iii) one may take $ c = 4\sqrt{2} $ . We obtain similar results for large classes of Hadamard spaces Y in the sense of Alexandrov.Type of Medium: Electronic ResourceURL: -
15Waldegger, S. ; Lang, U. ; Herzer, T. ; Suessbrich, H. ; Binder, K. ; Lepple-Wienhues, A. ; Lang, F. ; Busch, A. E. ; Nagl, U. ; Paulmichl, P. ; Franz, H. B. G. ; Kiesl, L.
Springer
Published 1996Staff ViewISSN: 1432-1912Keywords: K+ channel ; Estrogen ; Uterus ; ElectrophysiologySource: Springer Online Journal Archives 1860-2000Topics: MedicineNotes: Abstract Previously it was shown that minK protein expression in uterus is regulated by estrogen. In the present study, we were interested in putative direct effects of estrogen on minK protein induced K+ currents (IminK) in Xenopus oocytes. Superfusion with 17-β-estradiol (1 μM) resulted in an inhibition of minK-induced currents, but had no appreciable effects on the delayed rectifier and inward rectifier K+ channels Kv1.1 and Kir2.1, respectively. The inhibition of IminK by 17-β-estradiol was concentration-dependent, with an IC50 of approximately 0.5 μM. In the presence of 17-β-estradiol, the conductance-voltage relationship was shifted to more depolarized potentials. IminK inhibition occurred also in the presence of the estrogen-receptor antagonist tamoxifen, suggesting that a mechanism independent of estrogen receptors is involved. The synthetic estrogen diethylstilbestrol (DES) also inhibited IminK but with a lower affinity (IC50 of 4.5 μM), while cortisol and progesterone had only weak effects on IminK. In summary, the results indicate that estrogens directly inhibit IminK.Type of Medium: Electronic ResourceURL: -
16Waldegger, S. ; Lang, U. ; Herzer, T. ; Suessbrich, H. ; Binder, K. ; Lepple-Wienhues, A. ; Nagl, U. ; Paulmichl, M. ; Franz, H. B. G. ; Kiesl, L. ; Lang, F. ; Busch, A. E.
Springer
Published 1996Staff ViewISSN: 1432-1912Keywords: Key words K+ channel ; Estrogen ; Uterus ; ElectrophysiologySource: Springer Online Journal Archives 1860-2000Topics: MedicineNotes: Abstract Previously it was shown that minK protein expression in uterus is regulated by estrogen. In the present study, we were interested in putative direct effects of estrogen on minK protein induced K+ currents (IminK) in Xenopus oocytes. Superfusion with 17-β-estradiol (1 μM) resulted in an inhibition of minK-induced currents, but had no appreciable effects on the delayed rectifier and inward rectifier K+ channels Kv1.1 and Kir2.1, respectively. The inhibition of IminK by 17-β-estradiol was concentration-dependent, with an IC50 of approximately 0.5 μM. In the presence of 17-β-estradiol, the conductance-voltage relationship was shifted to more depolarized potentials. IminK inhibition occurred also in the presence of the estrogen-receptor antagonist tamoxifen, suggesting that a mechanism independent of estrogen receptors is involved. The synthetic estrogen diethylstilbestrol (DES) also inhibited IminK but with a lower affinity (IC50 of 4.5 μM), while cortisol and progesterone had only weak effects on IminK. In summary, the results indicate that estrogens directly inhibit IminK.Type of Medium: Electronic ResourceURL: -
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ISSN: 1432-0711Source: Springer Online Journal Archives 1860-2000Topics: MedicineType of Medium: Electronic ResourceURL: -
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ISSN: 1433-0393Keywords: Key words Uterine blood flow • Fetal growth • Growth restriction • Experimental IUGR ; Schlüsselwörter Uterine Durchblutung • Fetales Wachstum • Wachstumsrestriktion • Experimentelle IUWRSource: Springer Online Journal Archives 1860-2000Topics: MedicineDescription / Table of Contents: Zusammenfassung Eine adäquate uteroplazentare Perfusion während der gesamten Gestationsperiode ist eine Voraussetzung plazentaren und fetalen Wachstums bei Mensch und Tier. Grundlage der adäquaten uteroplazentaren Perfusion im Gestationsverlauf ist ein stetiger, physiologischer Anstieg der uterinen Durchblutung mit zunehmendem Gestationsalter. Das kardiovaskuläre System der Mutter erfährt während der Schwangerschaft grundlegende Veränderungen, um den Feten mit nutritiven Substanzen und mit Sauerstoff zu versorgen. Ein Anpassungsvorgang an die Gravidität besteht in der Erhöhung des Herzminutenvolumens, insbesondere durch Vermehrung des Plasmavolumens. Ebenso nimmt die Herzfrequenz der Schwangeren im Verlauf der Schwangerschaft gegenüber dem nicht schwangeren Zustand zu. Der Widerstand in der uterinen Strombahn sinkt, so daß sich die Uterusperfusion gegenüber dem nicht schwangeren Zustand dramatisch erhöht und unter physiologischen Bedingungen eine ausreichende Versorgung von Plazenta und Fet gewährleistet ist. Findet die Anpassung uteroplazentarer Perfusion nicht im benötigten Umfang statt, so drohen kompensatorische Wachstumsrestriktion und fetale Mangelversorgung bis hin zur intrauterinen Asphyxie.Notes: Summary An adequate increase of uterine blood flow throughout gestation is essential for uterine, placental and fetal growth. Maternal cardiovascular adaptation has to provide the uterine perfusion that is necessary to meet the requirements of the developing and growing fetus by providing transport of nutrients and oxygen to the placenta and the fetus. Thus uterine blood flow is inextricably linked to fetal growth and survival. Reductions of uterine blood flow can occur under acute or chronic conditions or in a combination of both. Chronic reductions of uterine blood flow can be observed in pregnancy induced hyertension (PIH), diabetes mellitus in pregnancy and intrauterine growth restriction (IUGR). Chronic restrictions in uterine blood flow will elicit a placental and fetal response in the form of growth adaptation to the reduced supply of oxygen and nutrients to the conceptus. If compensatory growth restriction reaches its limits intrauterine fetal distress can ensue.Type of Medium: Electronic ResourceURL: -
19Staff View
ISSN: 1433-0393Source: Springer Online Journal Archives 1860-2000Topics: MedicineType of Medium: Electronic ResourceURL: -
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ISSN: 1433-0393Source: Springer Online Journal Archives 1860-2000Topics: MedicineType of Medium: Electronic ResourceURL: