OpenURL Connection Search

Select item for more details and to access through your institution.

Effect of skin color on optical properties and the implications for medical optical technologies: a review.
Published in:
Journal of Biomedical Optics, 2024, v. 29, n. 1, p. 1, doi. 10.1117/1.JBO.29.1.010901
By:
- Setchfield, Kerry;
- Gorman, Alistair;
- Simpson, A. Hamish R. W.;
- Somekh, Michael G.;
- Wright, Amanda J.
Publication type:
Article
Development of hydrogel-based standards and phantoms for non-linear imaging at depth.
Published in:
Journal of Biomedical Optics, 2023, v. 28, n. 12, p. 126007, doi. 10.1117/1.JBO.28.12.126007
By:
- Haseeb, Fizza;
- Bourdakos, Konstantinos N.;
- Forsyth, Ewan;
- Setchfield, Kerry;
- Gorman, Alistair;
- Venkateswaran, Seshasailam;
- Wright, Amanda J.;
- Mahajan, Sumeet;
- Bradley, Mark
Publication type:
Article
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.
Published in:
Nature Genetics, 2013, v. 45, n. 7, p. 822, doi. 10.1038/ng.2637
By:
- Cordell, Heather J;
- Bentham, Jamie;
- Topf, Ana;
- Zelenika, Diana;
- Heath, Simon;
- Mamasoula, Chrysovalanto;
- Cosgrove, Catherine;
- Blue, Gillian;
- Granados-Riveron, Javier;
- Setchfield, Kerry;
- Thornborough, Chris;
- Breckpot, Jeroen;
- Soemedi, Rachel;
- Martin, Ruairidh;
- Rahman, Thahira J;
- Hall, Darroch;
- van Engelen, Klaartje;
- Moorman, Antoon F M;
- Zwinderman, Aelko H;
- Barnett, Phil
Publication type:
Article
Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls.
Published in:
Human Molecular Genetics, 2012, v. 21, n. 7, p. 1513, doi. 10.1093/hmg/ddr589
By:
- Soemedi, Rachel;
- Topf, Ana;
- Wilson, Ian J.;
- Darlay, Rebecca;
- Rahman, Thahira;
- Glen, Elise;
- Hall, Darroch;
- Huang, Ni;
- Bentham, Jamie;
- Bhattacharya, Shoumo;
- Cosgrove, Catherine;
- Brook, J. David;
- Granados-Riveron, Javier;
- Setchfield, Kerry;
- Bu'Lock, Frances;
- Thornborough, Chris;
- Devriendt, Koenraad;
- Breckpot, Jeroen;
- Hofbeck, Michael;
- Lathrop, Mark
Publication type:
Article
Combined Mutation Screening of NKX2-5, GATA4, and TBX5 in Congenital Heart Disease: Multiple Heterozygosity and Novel Mutations.
Published in:
Congenital Heart Disease, 2012, v. 7, n. 2, p. 151, doi. 10.1111/j.1747-0803.2011.00573.x
By:
- Granados-Riveron, Javier T.;
- Pope, Mark;
- Bu'Lock, Frances A.;
- Thornborough, Christopher;
- Eason, Jacqueline;
- Setchfield, Kerry;
- Ketley, Ami;
- Kirk, Edwin P.;
- Fatkin, Diane;
- Feneley, Michael P.;
- Harvey, Richard P.;
- Brook, J. David
Publication type:
Article
Label-free Brillouin endo-microscopy for the quantitative 3D imaging of sub-micrometre biology.
Published in:
Communications Biology, 2024, v. 7, n. 1, p. 1, doi. 10.1038/s42003-024-06126-4
By:
- La Cavera III, Salvatore;
- Chauhan, Veeren M.;
- Hardiman, William;
- Yao, Mengting;
- Fuentes-Domínguez, Rafael;
- Setchfield, Kerry;
- Abayzeed, Sidahmed A.;
- Pérez-Cota, Fernando;
- Smith, Richard J.;
- Clark, Matt
Publication type:
Article

Found: 6

Effect of skin color on optical properties and the implications for medical optical technologies: a review.

Development of hydrogel-based standards and phantoms for non-linear imaging at depth.

Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.

Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls.

Combined Mutation Screening of NKX2-5, GATA4, and TBX5 in Congenital Heart Disease: Multiple Heterozygosity and Novel Mutations.

Label-free Brillouin endo-microscopy for the quantitative 3D imaging of sub-micrometre biology.