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E Vielhaber

Explore the profile of E Vielhaber including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 11
Citations 259
Followers 0
Related Specialties
Genetics
Molecular Biology
Biochemistry
Top 10 Co-Authors
S S Sommer
R P Ketterling
C D Bottema
D M Virshup
D J Schaid
A Rivers
H S Yoon
M A Koerper
B Gostout
D P Jacobson
Published In
Hum Genet
Hum Mol Genet
Am J Hum Genet
Hum Mutat
Mol Cell Biol
Affiliations
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Recent Articles
1.
Casein kinase I: from obscurity to center stage
Vielhaber E, Virshup D
IUBMB Life . 2001 Jul; 51(2):73-8. PMID: 11463166
The casein kinase I (CKI) family of protein kinases is a group of highly related, ubiquitously expressed serine/threonine kinases found in all eukaryotic organisms from protozoa to man. Recent advances...
2.
Nuclear entry of the circadian regulator mPER1 is controlled by mammalian casein kinase I epsilon
Vielhaber E, Eide E, Rivers A, Gao Z, Virshup D
Mol Cell Biol . 2000 Jun; 20(13):4888-99. PMID: 10848614
The molecular oscillator that keeps circadian time is generated by a negative feedback loop. Nuclear entry of circadian regulatory proteins that inhibit transcription from E-box-containing promoters appears to be a...
3.
Germline origins in the human F9 gene: frequent G:C-->A:T mosaicism and increased mutations with advanced maternal age
Ketterling R, Vielhaber E, Li X, Drost J, Schaid D, Kasper C, et al.
Hum Genet . 2000 Jan; 105(6):629-40. PMID: 10647899
The factor IX gene (F9) is an advantageous system for analyzing recent spontaneous germline mutation in humans. Herein, the male:female ratio of mutation ("r") in F9 have been estimated by...
4.
Regulation of casein kinase I epsilon and casein kinase I delta by an in vivo futile phosphorylation cycle
Rivers A, Gietzen K, Vielhaber E, Virshup D
J Biol Chem . 1998 Jun; 273(26):15980-4. PMID: 9632646
Casein kinase I delta (CKIdelta) and casein kinase I epsilon (CKIepsilon) have been implicated in the response to DNA damage, but the understanding of how these kinases are regulated remains...
5.
The rates of G:C-->T:A and G:C-->C:G transversions at CpG dinucleotides in the human factor IX gene
Ketterling R, Vielhaber E, Sommer S
Am J Hum Genet . 1994 May; 54(5):831-5. PMID: 8178822
We have identified eight independent transversions at CpG in 290 consecutive families with hemophilia B. These eight transversions account for 16.3% of all independent transversions in our sample, yet the...
6.
Mutation detection, prenatal testing, and delineation of the germline origin in a family with sporadic hemophilia B and no living hemophiliacs
Vielhaber E, Sommer S, Freedenberg D
Am J Med Genet . 1994 Jan; 49(2):257-8. PMID: 8116680
No abstract available.
7.
Identification of mutations in four hemophilia B patients of Turkish origin, including a novel deletion of base 6411
Caglayan S, Vielhaber E, Gursel T, Aktuglu G, Sommer S
Hum Mutat . 1994 Jan; 4(2):163-5. PMID: 7981722
No abstract available.
8.
A mutation in the 3' untranslated region of the factor IX gene in four families with hemophilia B
Vielhaber E, Jacobson D, Ketterling R, Liu J, Sommer S
Hum Mol Genet . 1993 Aug; 2(8):1309-10. PMID: 8401514
No abstract available.
9.
The pattern of spontaneous germ-line mutation: relative rates of mutation at or near CpG dinucleotides in the factor IX gene
Bottema C, Ketterling R, Vielhaber E, Yoon H, Gostout B, Jacobson D, et al.
Hum Genet . 1993 Jun; 91(5):496-503. PMID: 8314564
Mutations at CpG dinucleotides were delineated in the factor IX gene of 38 hemophilia B patients. When transitions at CpG were considered with those previously reported by us and those...
10.
Germline mutations in the factor IX gene: a comparison of the pattern in Caucasians and non-Caucasians
Gostout B, Vielhaber E, Ketterling R, Yoon H, Bottema C, Kasper C, et al.
Hum Mol Genet . 1993 Mar; 2(3):293-8. PMID: 8499919
DNA samples of patients from around the world have been sequenced to precisely define the mutations in the factor IX gene resulting in hemophilia B. This study compares the patterns...