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C Papapetrou

Explore the profile of C Papapetrou including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 8
Citations 117
Followers 0
Related Specialties
Genetics
General Medicine
Biochemistry
Top 10 Co-Authors
Y H Edwards
S A Lynch
K Morrison
J Burn
P Scambler
W Reardon
L Spitz
M Barrow
I Frohn
C Meijers
Published In
Am J Hum Genet
Lancet
Genomics
Hum Mol Genet
Ann Hum Genet
Affiliations
Soon will be listed here.
Recent Articles
1.
Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene
Hagan D, Ross A, Strachan T, Lynch S, Wang Y, Scambler P, et al.
Am J Hum Genet . 2000 Apr; 66(5):1504-15. PMID: 10749657
The HLXB9 homeobox gene was recently identified as a locus for autosomal dominant Currarino syndrome, also known as hereditary sacral agenesis (HSA). This gene specifies a 403-amino acid protein containing...
2.
Mutations of UFD1L are not responsible for the majority of cases of DiGeorge Syndrome/velocardiofacial syndrome without deletions within chromosome 22q11
Wadey R, McKie J, Papapetrou C, Sutherland H, Lohman F, Osinga J, et al.
Am J Hum Genet . 1999 Jun; 65(1):247-9. PMID: 10364538
No abstract available.
3.
A genetic study of the human T gene and its exclusion as a major candidate gene for sacral agenesis with anorectal atresia
Papapetrou C, Drummond F, Reardon W, Winter R, Spitz L, Edwards Y
J Med Genet . 1999 Apr; 36(3):208-13. PMID: 10204846
Sacral agenesis is a heterogeneous group of congenital anomalies in which most cases are sporadic but rare familial forms also occur. Although one gene has been mapped to chromosome 7q36...
4.
Susceptibility to spina bifida; an association study of five candidate genes
Morrison K, Papapetrou C, Hol F, Mariman E, Lynch S, Burn J, et al.
Ann Hum Genet . 1999 Mar; 62(Pt 5):379-96. PMID: 10088035
Clues regarding candidate genes which influence susceptibility to spina bifida and anencephaly come from the identification of folate-associated risk factors and from studies of mouse mutants showing neural tube anomalies....
5.
The human TBX6 gene: cloning and assignment to chromosome 16p11.2
Papapetrou C, Putt W, Fox M, Edwards Y
Genomics . 1999 Feb; 55(2):238-41. PMID: 9933572
Tbx6 is a member of the T-box family of proteins, which share a region of homology corresponding to the DNA-binding domain of the transcription factor T. Previous expression studies and...
6.
The T transcription factor functions as a dimer and exhibits a common human polymorphism Gly-177-Asp in the conserved DNA-binding domain
Papapetrou C, Edwards Y, Sowden J
FEBS Lett . 1997 Jun; 409(2):201-6. PMID: 9202145
T is a transcription factor which activates transcription by binding to repeated arrangements of the dodecamer 5'-AGGTGTGAAATT-3'. Using in vitro synthesised T protein, we have demonstrated that T binds to...
7.
Methylenetetrahydrofolate reductase and neural tube defects
Papapetrou C, Lynch S, Burn J, Edwards Y
Lancet . 1996 Jul; 348(9019):58. PMID: 8691945
No abstract available.
8.
Genetic mapping of the human homologue (T) of mouse T(Brachyury) and a search for allele association between human T and spina bifida
Morrison K, Papapetrou C, Attwood J, Hol F, Lynch S, Sampath A, et al.
Hum Mol Genet . 1996 May; 5(5):669-74. PMID: 8733136
We describe a genetic analysis of the human homologue (T) of the mouse T (Brachyury) gene; human T was recently cloned in our laboratory. The protein product of the T...