scholarly journals Use of fluorescent in-situ hybridisation in salivary gland cytology: A powerful diagnostic tool

Cytopathology ◽  
2017 ◽  
Vol 28 (4) ◽  
pp. 312-320 ◽  
Author(s):  
S. M. Evrard ◽  
J. Meilleroux ◽  
G. Daniel ◽  
C. Basset ◽  
L. Lacoste-Collin ◽  
...  
Keyword(s):  
Salivary Gland ◽  
Diagnostic Tool ◽  
In Situ Hybridisation ◽  
Fluorescent In Situ Hybridisation ◽  
Powerful Diagnostic Tool

Fluorescent in situ hybridisation: A novel approach to salivary gland tumours

Pathology ◽  
2014 ◽  
Vol 46 ◽  
pp. S80
Author(s):  
Christina Selinger ◽  
Peter Luk ◽  
Jared Weston ◽  
Jonathan R. Clark ◽  
Sandra O’Toole ◽  
...  
Keyword(s):  
Salivary Gland ◽  
In Situ Hybridisation ◽  
Salivary Gland Tumours ◽  
Fluorescent In Situ Hybridisation ◽  
Novel Approach

Development of polymerase chain reaction and fluorescent in situ hybridisation techniques for the detection of a bacterial strain that degrades the cyanobacterial toxin microcystin LR

2005 ◽  
Vol 56 (8) ◽  
pp. 1127 ◽  
Author(s):  
D. G. Bourne ◽  
R. L. Blakeley ◽  
P. Riddles ◽  
G. J. Jones
Keyword(s):  
Polymerase Chain Reaction ◽  
Environmental Samples ◽  
In Situ Hybridisation ◽  
Cyanobacterial Blooms ◽  
Chain Reaction ◽  
Fluorescent In Situ Hybridisation ◽  
Cyanobacterial Toxin ◽  
Specific Amplification ◽  
Polymerase Chain

Polymerase chain reaction (PCR) and fluorescent in situ hybridisation (FISH) techniques were developed for the detection of a Sphingomonas bacterium (strain MJ-PV), previously demonstrated to degrade the cyanobacterial toxin microcystin LR. A PCR amplification protocol using the primer set Sph-f1008/Sph-r1243 demonstrated specific amplification of the target 16S ribosomal DNA (rDNA) of strain MJ-PV. A 16S ribosomal RNA (rRNA) targeted probe, Sph-r1264, labelled with a rhodamine fluorescent dye was successfully used in whole-cell FISH for the detection of MJ-PV in seeded controls. DNA primers and a PCR protocol were developed for the specific amplification of a gene, mlrA, which codes for the enzyme MlrA, responsible for hydrolysis of the cyanobacterial toxin microcystin LR. A survey using 16S rDNA and mlrA primers on extracted DNA from environmental samples of a lake that suffers regular toxic cyanobacterial blooms demonstrated no amplified products indicative of the presence of MJ-PV or mlrA. Although not detecting the MJ-PV strain in the tested environmental samples, these developed methods are useful to study the distribution of strain MJ-PV demonstrated to degrade mycrocystin LR in seeded bioremediation trails, as well as the distribution and the regulation of mlrA shown to be involved in mycrocystin LR degradation.

scholarly journals Unusual finding in the karyotype of a neonate with glandular hypospadias with chordee

2019 ◽  
Vol 12 (3) ◽  
pp. e228429
Author(s):  
Viraraghavan Vadakkencherry Ramaswamy ◽  
Gajanan Venkat Rao ◽  
Nori Suryanarayana ◽  
Sanghamitra Gummadapu
Keyword(s):  
Respiratory Distress ◽  
Y Chromosome ◽  
Clinical Finding ◽  
In Situ Hybridisation ◽  
Good Prognosis ◽  
Fluorescent In Situ Hybridisation ◽  
Parental Concerns ◽  
Unusual Finding

A 37-week, 2700 g vaginally delivered baby was admitted for respiratory distress which was attributed to transient tachypnoea of newborn. A clinical finding of glandular hypospadias with ventral chordee was detected. The penis was normal in size, and gonads were palpable bilaterally in the scrotal sac. The parents were informed of the good prognosis associated with this milder variety of hypospadias. In view of parental concerns, a fluorescent in situ hybridisation (FISH) for X and Y chromosome was performed. Surprisingly, FISH revealed the presence of 46, XY in 90% of cells and 46, XX in 10% of the remainder cells suggesting a diagnosis of chimerism.

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