R Mullenbach
Overview
Explore the profile of R Mullenbach including associated specialties, affiliations and a list of published articles.
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20
Citations
284
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Recent Articles
1.
Zimmer V, Krawczyk M, Mahler M, Weber S, Mullenbach R, Lammert F
Clin Exp Obstet Gynecol
. 2012 Jun;
39(1):32-5.
PMID: 22675952
Obstetric cholestasis (OC) is a cholestatic disorder with a prominent genetic background including variation in diverse hepatobiliary lipid transporters, such as ABCB4 (phospholipids) and ABCB11 (bile salts). Given a marked...
2.
Holzmann K, Mullenbach R, Blin N
Int J Oncol
. 2011 May;
3(2):261-4.
PMID: 21573357
DNA methylation appears to play an important role in both physiological and experimentally modified gene expression. Alterations in DNA methylation have been described in animal tumour models, in transformed cells...
3.
Mullenbach R, Bennett A, Tetlow N, Patel N, Hamilton G, Cheng F, et al.
Gut
. 2005 May;
54(6):829-34.
PMID: 15888793
Background: Intrahepatic cholestasis of pregnancy (ICP) affects approximately 0.7% of pregnancies in the UK and is associated with prematurity, fetal distress, and intrauterine death. Homozygous mutations in the ATP8B1 gene...
4.
Mullenbach R, Linton K, Wiltshire S, Weerasekera N, Chambers J, Elias E, et al.
J Med Genet
. 2003 May;
40(5):e70.
PMID: 12746424
No abstract available.
5.
Bertoni F, Mullenbach R, Broggini M, Roggero E, Cavalli F, Cotter F, et al.
Leuk Lymphoma
. 2000 Aug;
38(5-6):605-10.
PMID: 10953982
DNA amplification by polymerase chain reaction (PCR) with primers designed on the widely distributed Alu sequences allows the production of specific inter-Alu DNA-fingerprints. Amplification of tumour and matched normal DNA...
6.
Jones C, Mullenbach R, Grossfeld P, Auer R, Favier R, Chien K, et al.
Hum Mol Genet
. 2000 Apr;
9(8):1201-8.
PMID: 10767345
Folate-sensitive fragile sites are associated with the expansion and hypermethylation of CCG-repeats. The fragile site in 11q23.3, FRA11B, has been shown to cause chromosome deletions in vivo, its expression being...
7.
Liu Y, Corcoran M, Rasool O, Ivanova G, Ibbotson R, Grander D, et al.
Oncogene
. 1997 Dec;
15(20):2463-73.
PMID: 9395242
Previous studies have indicated the presence of a putative tumor suppressor gene on chromosome 13q14, commonly deleted in patients with B-cell chronic lymphocytic leukemia (B-CLL). We have previously defined a...
8.
Merscher S, Bekri S, de Leeuw B, Pedeutour F, Grosgeorge J, Shows T, et al.
Genomics
. 1997 Feb;
39(3):340-7.
PMID: 9119371
The distal part of 11q13, which contains several genes relevant to human diseases, has been poorly mapped as part of genome-wide mapping efforts. In the prospect of drawing a fine-scale...
9.
Blin N, Scholz M, Wissinger B, Mullenbach R, Pusch C
Mamm Genome
. 1997 Jan;
8(11):859-62.
PMID: 9337403
No abstract available.
10.
Pusch C, Mullenbach R, Gott P, Schmitt H, Wang Z, Roe B, et al.
Gene
. 1996 Dec;
183(1-2):29-33.
PMID: 8996083
Fifty cosmids from the ICRF, London, and Lawrence Livermore Laboratory, California, human chromosome 22 cosmid libraries were isolated, regionally assigned and tested for their ability to detect repeats or single...