Literature DB >> 10981148

What can knockout mice contribute to an understanding of hypertension?

L P Audoly1, T H Le, T M Coffman.   

Abstract

The generation of knockout mice using homologous recombination in embryonic stem cells is a powerful tool for physiologic investigations. This experimental approach has provided unique insights into the study of hypertension. Studies using knockout mice have shed new light on blood pressure regulatory mechanisms, molecular mechanisms of end-organ injury, and genetic mechanisms for hypertension. With the development of more accessible approaches for carrying out sophisticated manipulation of the mouse genome, there will be continuing utility of this technique for future studies of hypertension.

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Year:  2000        PMID: 10981148     DOI: 10.1007/s11906-000-0081-4

Source DB:  PubMed          Journal:  Curr Hypertens Rep        ISSN: 1522-6417            Impact factor:   5.369


  45 in total

Review 1.  Renin-angiotensin system: biochemistry and mechanisms of action.

Authors:  M J Peach
Journal:  Physiol Rev       Date:  1977-04       Impact factor: 37.312

2.  Renal proximal tubular AT2 receptor: signaling and transport.

Authors:  D Haithcock; H Jiao; X L Cui; U Hopfer; J G Douglas
Journal:  J Am Soc Nephrol       Date:  1999-01       Impact factor: 10.121

3.  Pressure-overload hypertrophy is unabated in mice devoid of AT1A receptors.

Authors:  M Hamawaki; T M Coffman; A Lashus; M Koide; M R Zile; M I Oliverio; G DeFreyte; G Cooper; B A Carabello
Journal:  Am J Physiol       Date:  1998-03

4.  Pressure overload induces cardiac hypertrophy in angiotensin II type 1A receptor knockout mice.

Authors:  K Harada; I Komuro; I Shiojima; D Hayashi; S Kudoh; T Mizuno; K Kijima; H Matsubara; T Sugaya; K Murakami; Y Yazaki
Journal:  Circulation       Date:  1998-05-19       Impact factor: 29.690

5.  Sustained hypersensitivity to angiotensin II and its mechanism in mice lacking the subtype-2 (AT2) angiotensin receptor.

Authors:  H M Siragy; T Inagami; T Ichiki; R M Carey
Journal:  Proc Natl Acad Sci U S A       Date:  1999-05-25       Impact factor: 11.205

6.  Communication between myocytes and fibroblasts in cardiac remodeling in angiotensin chimeric mice.

Authors:  T Matsusaka; H Katori; T Inagami; A Fogo; I Ichikawa
Journal:  J Clin Invest       Date:  1999-05-15       Impact factor: 14.808

7.  Increased renal vasodilator prostanoids prevent hypertension in mice lacking the angiotensin subtype-2 receptor.

Authors:  H M Siragy; T Senbonmatsu; T Ichiki; T Inagami; R M Carey
Journal:  J Clin Invest       Date:  1999-07       Impact factor: 14.808

8.  Identification of two subtypes in the rat type I angiotensin II receptor.

Authors:  N Iwai; T Inagami
Journal:  FEBS Lett       Date:  1992-02-24       Impact factor: 4.124

9.  Mice lacking angiotensin-converting enzyme have low blood pressure, renal pathology, and reduced male fertility.

Authors:  C R Esther; T E Howard; E M Marino; J M Goddard; M R Capecchi; K E Bernstein
Journal:  Lab Invest       Date:  1996-05       Impact factor: 5.662

10.  Angiotensin-converting enzyme gene polymorphism is associated with myocardial infarction but not with development of coronary stenosis.

Authors:  E Ludwig; P S Corneli; J L Anderson; H W Marshall; J M Lalouel; R H Ward
Journal:  Circulation       Date:  1995-04-15       Impact factor: 29.690

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  1 in total

Review 1.  Dopamine receptor-coupling defect in hypertension.

Authors:  Pedro A Jose; Gilbert M Eisner; Robin A Felder
Journal:  Curr Hypertens Rep       Date:  2002-06       Impact factor: 5.369

  1 in total

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