From molecule to men: molecular basis of congenital cardiovascular disorders
Gespeichert in:
| Weitere beteiligte Personen: | , , |
|---|---|
| Format: | Buch |
| Sprache: | Englisch |
| Veröffentlicht: |
Darmstadt [u.a.]
Steinkopff [u.a.]
2000
New York Springer |
| Schlagwörter: | |
| Links: | http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=008661154&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |
| Umfang: | X, 246 S. Ill., graph. Darst. |
| ISBN: | 3798511683 |
Internformat
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| 245 | 1 | 0 | |a From molecule to men |b molecular basis of congenital cardiovascular disorders |c M. Zehender, G. Breithardt, H. Just, editors |
| 264 | 1 | |a Darmstadt [u.a.] |b Steinkopff [u.a.] |c 2000 | |
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Datensatz im Suchindex
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| adam_text | Contents
Foreword , V
Molecular Basis of Congenital Cardiovascular Disorders
Genetics of dilated cardiomyopathy
Thierfelder, L • . 1
Registry of families with inherited dilated cardiomyopathy for molecular
analyses
Franz, W. M., O. J. Miiller, E. Griinig, M. Cremer, H. A. Katus • , 7
Distinct phenotype patterns of Ca2+ handling proteins in end stage failing
human hearts
Pieske, B., W. Schillinger, S. Dieterich, L. S. Maier, G. Hasenfuss, J. Prestle .. ¦ . 19
Apoptosis in the overloaded myocardium: potential stimuli and modifying
signals
Schumann, H., H. Heinrich, B. Bartling, D. Darmer, J. Holtz , 33
Analysis of inherited causes of hypertrophic cardiomyopathy as part of
clinical practice
Vosberg, H. R, J. Moolman, C. Dohlemann, P. McKeown, S. Reith , 69
Molecular genetics of arrhythmogenic right ventricular cardiomyopathy
Rampazzo, A., A. Nava, M. Miorin, N. Tiso, G. Thieme, G. A. Danieli • , 77
Cardiomyopathy: Genetics in muscular dystrophies
Rocco, C, S. Miocic, L. Mestroni ¦ 81
Molecular impact of ion channel mutations for the pathogenesis of long QT
(LQT) syndromes
Schulze Bahr, E., H. Wedekind, W. Haverkamp, M. Borggrefe, G. Breithardt,
H. Funke 85
Acquired abnormal QT prolongation and torsade de pointes clinical
significance of genetic information from congenital long QT syndrome
Haverkamp, W., G. Monnig, L. Eckhardt, P. Kirchhof, H. Wedekind,
E. Schulze Bahr, H. Funke, M. Borggrefe, G. Breithardt 99
Molecular genetic approaches to human hypertension
Luft, EC 113
Renin angiotensin system and coronary artery disease Interaction of
angiotensin II with pro inflammatory cytokines in human stable and unstah|e
coronary plaques
Schieffer, B., H. Drexler . 127
Genetics of Lipoprotein(a)
Kraft, H. G 143
The molecular mechanisms of inherited hy percholesterolemia
Marz, W., M. S. Nauck, E. Fisher, M. M. Hoffmann, H. Wieland 151
Insulin resistance: A pathogenic link between cardiovascular risk factors
and atherosclerosis
Muller Wieland, D., J. Kotzka, B. Knebel, J. Briining, W. Krone 171
Genetic control of hemostatic factors in relation to atherosclerosis
Schuttrumpf, J., H. H. Watzke 179
Increased platelet aggregability associated with platelet GPIIIa PIA2
polymorphism: the Framingham Offspring Study
Feng D., K. Lindpainter, M. G. Larson, V. S. Rao, C. J. O Donnel. I. Lipinska,
C. Schmitz, P. A. Sutherland, H. Silbershatz, R. B. D Agostino, J. E. Muller,
R. H. Myers, D. Levy, G. H. Tofler 189
Genetic aspects of chronobiologic rhythms in cardiovascular disease
Lemmer, B 201
Is capillary sprouting enough?
Buschmann, I., W. Schaper 215
Angiogenesis and gene therapy
Schratzberger, P., J. M. Isner 221
Genetic engineering for human bypass vein grafts
Mann, M. J 233
Molecular cardiology and physician
Taylor, S. H 243
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| genre_facet | Konferenzschrift 1998 Gargellen |
| id | DE-604.BV012736984 |
| illustrated | Illustrated |
| indexdate | 2024-12-20T10:35:26Z |
| institution | BVB |
| isbn | 3798511683 |
| language | English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-008661154 |
| oclc_num | 231855619 |
| open_access_boolean | |
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| owner_facet | DE-355 DE-BY-UBR DE-12 DE-11 |
| physical | X, 246 S. Ill., graph. Darst. |
| publishDate | 2000 |
| publishDateSearch | 2000 |
| publishDateSort | 2000 |
| publisher | Steinkopff [u.a.] Springer |
| record_format | marc |
| spellingShingle | From molecule to men molecular basis of congenital cardiovascular disorders Herzkrankheit (DE-588)4024663-2 gnd Erbkrankheit (DE-588)4015106-2 gnd Molekularbiologie (DE-588)4039983-7 gnd Molekularpathologie (DE-588)4170396-0 gnd Angeborene Krankheit (DE-588)4331107-6 gnd |
| subject_GND | (DE-588)4024663-2 (DE-588)4015106-2 (DE-588)4039983-7 (DE-588)4170396-0 (DE-588)4331107-6 (DE-588)1071861417 |
| title | From molecule to men molecular basis of congenital cardiovascular disorders |
| title_auth | From molecule to men molecular basis of congenital cardiovascular disorders |
| title_exact_search | From molecule to men molecular basis of congenital cardiovascular disorders |
| title_full | From molecule to men molecular basis of congenital cardiovascular disorders M. Zehender, G. Breithardt, H. Just, editors |
| title_fullStr | From molecule to men molecular basis of congenital cardiovascular disorders M. Zehender, G. Breithardt, H. Just, editors |
| title_full_unstemmed | From molecule to men molecular basis of congenital cardiovascular disorders M. Zehender, G. Breithardt, H. Just, editors |
| title_short | From molecule to men |
| title_sort | from molecule to men molecular basis of congenital cardiovascular disorders |
| title_sub | molecular basis of congenital cardiovascular disorders |
| topic | Herzkrankheit (DE-588)4024663-2 gnd Erbkrankheit (DE-588)4015106-2 gnd Molekularbiologie (DE-588)4039983-7 gnd Molekularpathologie (DE-588)4170396-0 gnd Angeborene Krankheit (DE-588)4331107-6 gnd |
| topic_facet | Herzkrankheit Erbkrankheit Molekularbiologie Molekularpathologie Angeborene Krankheit Konferenzschrift 1998 Gargellen |
| url | http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=008661154&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |
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