74 results filtered with: Fluorescent Dyes
- Digital Images
- Online
Turner's stndrome, centromere & cosmid probe
Wessex Reg. Genetics Centre
- Digital Images
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Human HeLa cancer cells, mitosis
Paul Andrews/Univ. Dundee
- Digital Images
- Online
Amyloid deposition in Type II diabetes pancreas islets
Anne Clark, University of Oxford
- Digital Images
- Online
Pressure palsy, deletion c'some 17, cosmid
Wessex Reg. Genetics Centre
- Digital Images
- Online
Section through neural tube of chick embryo, confocal
Arwen Wilcock/Univ. Dundee
- Digital Images
- Online
Human HeLa cancer cells, prometaphase
Paul Andrews/Univ. Dundee
- Digital Images
- Online
Translocation shown using centromere probes
Wessex Reg. Genetics Centre
- Digital Images
- Online
Familial aniridia deletion shown by cosmid
Wessex Reg. Genetics Centre
- Digital Images
- Online
Human HeLa cancer cell, tripolar mitosis
Paul Andrews/Univ. Dundee
- Digital Images
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Prader Willi & Angelman's syndromes - probes
Wessex Reg. Genetics Centre
- Digital Images
- Online
Duchenne muscular dystrophy deletion, FISH
Wessex Reg. Genetics Centre
- Digital Images
- Online
Translocation - use of cosmid probe
Wessex Reg. Genetics Centre
- Digital Images
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Human HeLa cancer cells, cytokinesis
Paul Andrews/Univ. Dundee
- Digital Images
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DNA sequencing using cosmids for c'some 9
Dr Rosemary Ekong, UCL- Books
Ueber die Wirkung fluorescirender Stoffe auf Infusorien / von Oscar Raab.
Raab, Oscar.Date: 1900
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Human HeLa cancer cell chromosome rosettes
Paul Andrews/Univ. Dundee
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Xenopus cancer kidney cells, interphase
Paul Andrews/Univ. Dundee
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Human HeLa cancer cells, stages of mitosis
William J Moore/Univ. Dundee- Books
Fluorescent protein tracing / edited by R.C. Nairn.
Date: 1969
- Digital Images
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Aniridia + deletion, FISH probes
Wessex Reg. Genetics Centre
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Human cancer cell
Elena Knatko/Univ. Dundee
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Translocation shown up by cosmid probe
Wessex Reg. Genetics Centre
- Digital Images
- Online
Human HeLa cancer cell in prometaphase of mitosis
William J Moore/Univ. Dundee
- Digital Images
- Online
Duchenne muscular dystrophy control, FISH
Wessex Reg. Genetics Centre
- Digital Images
- Online
Duchenne muscular dystrophy - normal female, chromosomes have been highlighted by a fluorescent probe for exon 45/47 (note the double yellow band). This disorder is caused by a recessive gene on the X chromosome, so is normally shown only by males, who lack a second X chromosome. The condition starts with difficulty in walking and climbing stairs in early childhood, usually resulting in confinement to a wheelchair by the age of 10, with death from respiratory infection or cardiac failure by about the age of 20.
Wessex Reg. Genetics Centre