Fleck E - Search Results

1

Genetic variants in the promoter (g983G>T) and coding region (A92T) of the human cardiotrophin-1 gene (CTF1) in patients with dilated cardiomyopathy.

Erdmann J, Hassfeld S, Kallisch H, Fleck E, Regitz-Zagrose V. Erdmann J, et al. Among authors: fleck e. Hum Mutat. 2000 Nov;16(5):448. doi: 10.1002/1098-1004(200011)16:5<448::AID-HUMU19>3.0.CO;2-D. Hum Mutat. 2000. PMID: 11058912 No abstract available.

2

Cloning and characterization of the 5'-flanking region of the human cardiotrophin-1 gene.

Erdmann J, Hassfeld S, Kallisch H, Fleck E, Regitz-Zagrosek V. Erdmann J, et al. Among authors: fleck e. Biochem Biophys Res Commun. 1998 Mar 17;244(2):494-7. doi: 10.1006/bbrc.1998.8311. Biochem Biophys Res Commun. 1998. PMID: 9514957

3

Novel intronic polymorphism (+1675G/A) in the human angiotensin II subtype 2 receptor gene.

Erdmann J, Guse M, Kallisch H, Fleck E, Regitz-Zagrosek V. Erdmann J, et al. Among authors: fleck e. Hum Mutat. 2000 May;15(5):487. doi: 10.1002/(SICI)1098-1004(200005)15:5<487::AID-HUMU29>3.0.CO;2-D. Hum Mutat. 2000. PMID: 10790229 No abstract available.

4

Five novel genetic variants in the promoter and coding region of the alpha B-crystallin gene (CRYAB): -652G>A, -650C>G, -249G>C, S41Y, P51L.

Hahner A, Erdmann J, Kallisch H, Fleck E, Regitz-Zagrosek V. Hahner A, et al. Among authors: fleck e. Hum Mutat. 2000 Oct;16(4):374. doi: 10.1002/1098-1004(200010)16:4<374::AID-HUMU17>3.0.CO;2-Z. Hum Mutat. 2000. PMID: 11013455 No abstract available.

5

Identification of genetic variants (g789C>T and G111S) in the human HSPB2 gene.

Hahner A, Erdmann J, Kallisch H, Fleck E, Regitz-Zagrosek V. Hahner A, et al. Among authors: fleck e. Hum Mutat. 2001;17(1):81. doi: 10.1002/1098-1004(2001)17:1<81::AID-HUMU29>3.0.CO;2-7. Hum Mutat. 2001. PMID: 11139265 No abstract available.

6

Screening the human bradykinin B2 receptor gene in patients with cardiovascular diseases: identification of a functional mutation in the promoter and a new coding variant (T21M).

Erdmann J, Hegemann N, Weidemann A, Kallisch H, Hummel M, Hetzer R, Fleck E, Regitz-Zagrosek V. Erdmann J, et al. Among authors: fleck e. Am J Med Genet. 1998 Dec 28;80(5):521-5. Am J Med Genet. 1998. PMID: 9880221

7

Characterization of polymorphisms in the promoter of the human angiotensin II subtype 1 (AT1) receptor gene.

Erdmann J, Riedel K, Rohde K, Folgmann I, Wienker T, Fleck E, Regitz-Zagrosek V. Erdmann J, et al. Among authors: fleck e. Ann Hum Genet. 1999 Jul;63(Pt 4):369-74. doi: 10.1046/j.1469-1809.1999.6340369.x. Ann Hum Genet. 1999. PMID: 10738546

8

Novel mutation in the alpha-tropomyosin gene and transition from hypertrophic to hypocontractile dilated cardiomyopathy.

Regitz-Zagrosek V, Erdmann J, Wellnhofer E, Raible J, Fleck E. Regitz-Zagrosek V, et al. Among authors: fleck e. Circulation. 2000 Oct 24;102(17):E112-6. doi: 10.1161/01.cir.102.17.e112. Circulation. 2000. PMID: 11044437 No abstract available.

9

Spectrum of clinical phenotypes and gene variants in cardiac myosin-binding protein C mutation carriers with hypertrophic cardiomyopathy.

Erdmann J, Raible J, Maki-Abadi J, Hummel M, Hammann J, Wollnik B, Frantz E, Fleck E, Hetzer R, Regitz-Zagrosek V. Erdmann J, et al. Among authors: fleck e. J Am Coll Cardiol. 2001 Aug;38(2):322-30. doi: 10.1016/s0735-1097(01)01387-0. J Am Coll Cardiol. 2001. PMID: 11499719 Free article.

10

Genetic polymorphisms of the angiotensin II type 1 (AT1) receptor gene.

Rolfs A, Weber-Rolfs I, Regitz-Zagrosek V, Kallisch H, Riedel K, Fleck E. Rolfs A, et al. Among authors: fleck e. Eur Heart J. 1994 Dec;15 Suppl D:108-12. doi: 10.1093/eurheartj/15.suppl_d.108. Eur Heart J. 1994. PMID: 7713099

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