V P COLLINS - JoVE Visualize

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Genomics|November 1, 1991

A map of 22 loci on human chromosome 22J P Dumanski, E Carlbom, V P Collins, et al.

Human Molecular Genetics|August 1, 1994

Characterization of a new member of the human beta-adaptin gene family from chromosome 22q12, a candidate meningioma geneM Peyrard, I Fransson, Y G Xie, et al.

Oncogene|October 16, 2007

1p36 is a preferential target of chromosome 1 deletions in astrocytic tumours and homozygously deleted in a subset of glioblastomasK Ichimura, A P Vogazianou, L Liu, et al.

Leukemia|December 1, 1995

KBM-7, a human myeloid leukemia cell line with double Philadelphia chromosomes lacking normal c-ABL and BCR transcriptsB S Andersson, V P Collins, R Kurzrock, et al.

Neurology|September 1, 1993

Presymptomatic diagnosis for neurofibromatosis 2 with chromosome 22 markersM H Ruttledge, S A Narod, J P Dumanski, et al.

The American Journal of Pathology|January 1, 1989

Neuroblastic differentiation potential of the human retinoblastoma cell lines Y-79 and WERI-Rb1 maintained in an organ culture system. An immunohistochemical, electron microscopic, and biochemical studyM M Herman, E Perentes, C D Katsetos, et al.

Journal of Neurochemistry|October 1, 1990

Determination of gangliosides in six human primary medulloblastomasJ Gottfries, P Fredman, J E Månsson, et al.

American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|July 16, 2003

Treatment of graft-versus-host disease after liver transplantation with basiliximab followed by bowel resectionS Sudhindran, A Taylor, L Delriviere, et al.

Oncogene|December 18, 2007

Array painting reveals a high frequency of balanced translocations in breast cancer cell lines that break in cancer-relevant genesK D Howarth, K A Blood, B L Ng, et al.

Brain Pathology (Zurich, Switzerland)|April 18, 1998

Frequent inactivation of CDKN2A and rare mutation of TP53 in PCNSLJ M Cobbers, M Wolter, J Reifenberger, et al.

Pageof 21

Showing results (191-200 of 201) with videos related to

Sort By:

Pageof 21

Genomics|November 1, 1991

A map of 22 loci on human chromosome 22J P Dumanski, E Carlbom, V P Collins, et al.

Human Molecular Genetics|August 1, 1994

Characterization of a new member of the human beta-adaptin gene family from chromosome 22q12, a candidate meningioma geneM Peyrard, I Fransson, Y G Xie, et al.

Oncogene|October 16, 2007

1p36 is a preferential target of chromosome 1 deletions in astrocytic tumours and homozygously deleted in a subset of glioblastomasK Ichimura, A P Vogazianou, L Liu, et al.

Leukemia|December 1, 1995

KBM-7, a human myeloid leukemia cell line with double Philadelphia chromosomes lacking normal c-ABL and BCR transcriptsB S Andersson, V P Collins, R Kurzrock, et al.

Neurology|September 1, 1993

Presymptomatic diagnosis for neurofibromatosis 2 with chromosome 22 markersM H Ruttledge, S A Narod, J P Dumanski, et al.

The American Journal of Pathology|January 1, 1989

Journal of Neurochemistry|October 1, 1990

Determination of gangliosides in six human primary medulloblastomasJ Gottfries, P Fredman, J E Månsson, et al.

American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|July 16, 2003

Treatment of graft-versus-host disease after liver transplantation with basiliximab followed by bowel resectionS Sudhindran, A Taylor, L Delriviere, et al.

Oncogene|December 18, 2007

Array painting reveals a high frequency of balanced translocations in breast cancer cell lines that break in cancer-relevant genesK D Howarth, K A Blood, B L Ng, et al.

Brain Pathology (Zurich, Switzerland)|April 18, 1998

Frequent inactivation of CDKN2A and rare mutation of TP53 in PCNSLJ M Cobbers, M Wolter, J Reifenberger, et al.

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