P Scambler
Overview
Explore the profile of P Scambler including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
58
Citations
2198
Followers
0
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Recent Articles
1.
Lau K, Diaz-Zuccarini V, Scambler P, Burriesci G
J Biomech
. 2011 Jul;
44(13):2409-17.
PMID: 21767842
The effect of functional mitral regurgitation has been investigated in an anatomically sized, fluid-structure interaction mitral valve model, where simulated correction has been performed by applying: (1) edge-to-edge repair with...
2.
Lau K, Diaz V, Scambler P, Burriesci G
Med Eng Phys
. 2010 Aug;
32(9):1057-64.
PMID: 20702128
Modelling and simulation of heart valves is a challenging biomechanical problem due to anatomical variability, pulsatile physiological pressure loads and 3D anisotropic material behaviour. Current valvular models based on the...
3.
Pitera J, Milla P, Scambler P, Adjaye J
Mech Dev
. 2001 Dec;
109(2):377-81.
PMID: 11731253
We describe the cloning of HOXD1 in human unfertilised oocytes and detailed expression analyses during mouse oogenesis and embryogenesis. The cDNA of 1991bp has an open reading frame of 987bp...
4.
Dechairo B, Dimon C, van Heel D, Mackay I, Edwards M, Scambler P, et al.
Eur J Hum Genet
. 2001 Aug;
9(8):627-33.
PMID: 11528509
Inflammatory bowel disease (IBD) is a chronic inflammatory disease of the intestine, commonly diagnosed as either ulcerative colitis (UC) or Crohn's disease (CD). Epidemiological studies have consistently shown that both...
5.
Merscher S, Funke B, Epstein J, HEYER J, Puech A, Lu M, et al.
Cell
. 2001 Mar;
104(4):619-29.
PMID: 11239417
Velo-cardio-facial syndrome (VCFS)/DiGeorge syndrome (DGS) is a human disorder characterized by a number of phenotypic features including cardiovascular defects. Most VCFS/DGS patients are hemizygous for a 1.5-3.0 Mb region of...
6.
Bird L, Scambler P
Clin Genet
. 2000 Aug;
58(1):64-8.
PMID: 10945664
Two patients with chromosome 22q11 deletion and cortical dysgenesis (gyral abnormalities) are reported in this study. One had unilateral clubfoot in addition to multiple features suggestive of the Di George...
7.
Koziell A, Charmandari E, Hindmarsh P, Rees L, Scambler P, Brook C
Clin Endocrinol (Oxf)
. 2000 Apr;
52(4):519-24.
PMID: 10762296
Dysfunction of the Wilms' Tumour gene (WT1), a transcription factor critical for normal development and function of the urogenital tract, can result in both tumourigenesis [corrected] and urogenital abnormalities. The...
8.
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...
9.
Seroussi E, Kedra D, Pan H, Peyrard M, Schwartz C, Scambler P, et al.
Genome Res
. 1999 Oct;
9(9):803-14.
PMID: 10508838
Analysis of 600 kb of sequence encompassing the beta-prime adaptin (BAM22) gene on human chromosome 22 revealed intrachromosomal duplications within 22q12-13 resulting in three active RFPL genes, two RFPL pseudogenes,...
10.
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.