Finckh U - Search Results

1

NPC1: Complete genomic sequence, mutation analysis, and characterization of haplotypes.

Bauer P, Knoblich R, Bauer C, Finckh U, Hufen A, Kropp J, Braun S, Kustermann-Kuhn B, Schmidt D, Harzer K, Rolfs A. Bauer P, et al. Among authors: finckh u. Hum Mutat. 2002 Jan;19(1):30-8. doi: 10.1002/humu.10016. Hum Mutat. 2002. PMID: 11754101

2

Simple PCR amplification of the entire glucocerebrosidase gene (GBA) coding region for diagnostic sequence analysis.

Finckh U, Seeman P, von Widdern OC, Rolfs A. Finckh U, et al. DNA Seq. 1998;8(6):349-56. doi: 10.3109/10425179809020896. DNA Seq. 1998. PMID: 10728820

3

Dopamine D2 receptor gene (DRD2) haplotypes in Caucasians.

Finckh U, Giraldo-Velasquez M, Pelz J, Otto G, Sander T, Schmidt LG, Rommelspacher H, Rolfs A. Finckh U, et al. Gene. 1996 Nov 14;179(2):251-5. doi: 10.1016/s0378-1119(96)00369-1. Gene. 1996. PMID: 8972908

4

Two new missense mutations in a non-Jewish Caucasian family with type 3 Gaucher disease.

Seeman PJ, Finckh U, Höppner J, Lakner V, Liebisch I, Grau G, Rolfs A. Seeman PJ, et al. Among authors: finckh u. Neurology. 1996 Apr;46(4):1102-7. doi: 10.1212/wnl.46.4.1102. Neurology. 1996. PMID: 8780099

5

Allele-specific PCR for simultaneous amplification of both alleles of a deletion polymorphism in intron 6 of the human dopamine 2 receptor gene (DRD2).

Finckh U, Rommelspacher H, Schmidt LG, Rolfs A. Finckh U, et al. DNA Seq. 1996;6(2):87-94. doi: 10.3109/10425179609010195. DNA Seq. 1996. PMID: 8907305

6

Absence of angiotensin II type 1 receptor gene mutations in human adrenal tumors.

Sachse R, Shao XJ, Rico A, Finckh U, Rolfs A, Reincke M, Hensen J. Sachse R, et al. Among authors: finckh u. Eur J Endocrinol. 1997 Sep;137(3):262-6. doi: 10.1530/eje.0.1370262. Eur J Endocrinol. 1997. PMID: 9330590

7

Amplification of Mycobacterium tuberculosis from peripheral blood.

Rolfs A, Beige J, Finckh U, Köhler B, Schaberg T, Lokies J, Lode H. Rolfs A, et al. Among authors: finckh u. J Clin Microbiol. 1995 Dec;33(12):3312-4. doi: 10.1128/jcm.33.12.3312-3314.1995. J Clin Microbiol. 1995. PMID: 8586724 Free PMC article. Clinical Trial.

8

Allelic association of a dopamine transporter gene polymorphism in alcohol dependence with withdrawal seizures or delirium.

Sander T, Harms H, Podschus J, Finckh U, Nickel B, Rolfs A, Rommelspacher H, Schmidt LG. Sander T, et al. Among authors: finckh u. Biol Psychiatry. 1997 Feb 1;41(3):299-304. doi: 10.1016/s0006-3223(96)00044-3. Biol Psychiatry. 1997. PMID: 9024952 Clinical Trial.

9

No association of the structural dopamine D2 receptor (DRD2) variant 311Cys with alcoholism.

Finckh U, von Widdern O, Giraldo-Velasquez M, Podschus J, Dufeu P, Sander T, Harms H, Schmidt LG, Rommelspacher H, Rolfs A. Finckh U, et al. Alcohol Clin Exp Res. 1996 May;20(3):528-32. doi: 10.1111/j.1530-0277.1996.tb01087.x. Alcohol Clin Exp Res. 1996. PMID: 8727249

10

Novel CCM1, CCM2, and CCM3 mutations in patients with cerebral cavernous malformations: in-frame deletion in CCM2 prevents formation of a CCM1/CCM2/CCM3 protein complex.

Stahl S, Gaetzner S, Voss K, Brackertz B, Schleider E, Sürücü O, Kunze E, Netzer C, Korenke C, Finckh U, Habek M, Poljakovic Z, Elbracht M, Rudnik-Schöneborn S, Bertalanffy H, Sure U, Felbor U. Stahl S, et al. Among authors: finckh u. Hum Mutat. 2008 May;29(5):709-17. doi: 10.1002/humu.20712. Hum Mutat. 2008. PMID: 18300272

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

66 results

Search Page