Kulvinder Kaur

VACTERL/caudal regression/Currarino syndrome-like malformations in mice with mutation in the proprotein convertase Pcsk5 (2008)

Szumska, Dorota, Pieles, Guido, Essalmani, Rachid, Bilski, Michal, Mesnard, Daniel, Kaur, Kulvinder, ...

We have identified an ethylnitrosourea (ENU)-induced recessive mouse mutation (Vcc) with a pleiotropic phenotype that includes cardiac, tracheoesophageal, anorectal, anteroposterior patterning...

Matrix-Assisted Laser Desorption/Ionisation, Time-of-Flight Mass Spectrometry in Genomics Research (2006)

Jiannis Ragoussis, Gareth P. Elvidge, Kulvinder Kaur, Stefano Colella

The beginning of this millennium has seen dramatic advances in genomic research. Milestones such as the complete sequencing of the human genome and of many other species were achieved and...

Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen

Bogani, Debora, Willoughby, Catherine, Davies, Jennifer, Kaur, Kulvinder, Mirza, Ghazala, Paudyal, Anju, ...

Monosomy of the human chromosome 6p terminal region results in a variety of congenital malformations that include brain, craniofacial, and organogenesis abnormalities. To examine the genetic basis of...

Matrix-Assisted Laser Desorption/Ionisation, Time-of-Flight Mass Spectrometry in Genomics Research

Ragoussis, Jiannis, Elvidge, Gareth P, Kaur, Kulvinder, Colella, Stefano

The beginning of this millennium has seen dramatic advances in genomic research. Milestones such as the complete sequencing of the human genome and of many other species were achieved and...

Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen

Bogani, Debora, Willoughby, Catherine, Davies, Jennifer, Kaur, Kulvinder, Mirza, Ghazala, Paudyal, Anju, ...

Monosomy of the human chromosome 6p terminal region results in a variety of congenital malformations that include brain, craniofacial, and organogenesis abnormalities. To examine the genetic basis of...

Matrix-Assisted Laser Desorption/Ionisation, Time-of-Flight Mass Spectrometry in Genomics Research

Ragoussis, Jiannis, Elvidge, Gareth P, Kaur, Kulvinder, Colella, Stefano

The beginning of this millennium has seen dramatic advances in genomic research. Milestones such as the complete sequencing of the human genome and of many other species were achieved and...

VACTERL/caudal regression/Currarino syndrome-like malformations in mice with mutation in the proprotein convertase Pcsk5

Szumska, Dorota, Pieles, Guido, Essalmani, Rachid, Bilski, Michal, Mesnard, Daniel, Kaur, Kulvinder, ...

We have identified an ethylnitrosourea (ENU)-induced recessive mouse mutation (Vcc) with a pleiotropic phenotype that includes cardiac, tracheoesophageal, anorectal, anteroposterior patterning...