D H Wreschner|G Rechavi - JoVE Visualize

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Acta Haematologica|January 1, 1997

Ubiquitous expression of a cloned murine thymopoietin cDNAL Theodor, J Shoham, R Berger, et al.

Leukemia|July 30, 2002

Chimerism testing and detection of minimal residual disease after allogeneic hematopoietic transplantation using the bioView (Duet) combined morphological and cytogenetical analysisA Shimoni, A Nagler, C Kaplinsky, et al.

Leukemia|October 14, 2006

Gene expression profiles of AML derived stem cells; similarity to hematopoietic stem cellsH Gal, N Amariglio, L Trakhtenbrot, et al.

Medical and Pediatric Oncology|February 1, 1997

Central nervous system involvement at diagnosis in a case of pediatric CD30+ anaplastic large cell lymphomaC Kaplinsky, A Toren, Y Neumann, et al.

Bone Marrow Transplantation|April 1, 1999

Successful human umbilical cord blood stem cell transplantation without conditioning in severe combined immune deficiencyA Toren, A Nagler, N Amariglio, et al.

Journal of Cell Science|October 10, 2001

Nuclear membrane protein LAP2beta mediates transcriptional repression alone and together with its binding partner GCL (germ-cell-less)E Nili, G S Cojocaru, Y Kalma, et al.

Transplantation|October 25, 2000

Amplification of immunological functions by subcutaneous injection of intermediate-high dose interleukin-2 for 2 years after autologous stem cell transplantation in children with stage IV neuroblastomaA Toren, A Nagler, G Rozenfeld-Granot, et al.

Clinical Genetics|July 4, 2015

SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosumG Heimer, D Marek-Yagel, E Eyal, et al.

Lung Cancer (Amsterdam, Netherlands)|January 30, 2007

Chromosomal aberrations and gene expression profiles in non-small cell lung cancerE Dehan, A Ben-Dor, W Liao, et al.

Journal of Medical Genetics|July 22, 2005

The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardationL Basel-Vanagaite, R Attia, M Yahav, et al.

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Showing results (171-180 of 183) with videos related to

Sort By:

Pageof 19

Acta Haematologica|January 1, 1997

Ubiquitous expression of a cloned murine thymopoietin cDNAL Theodor, J Shoham, R Berger, et al.

Leukemia|July 30, 2002

Chimerism testing and detection of minimal residual disease after allogeneic hematopoietic transplantation using the bioView (Duet) combined morphological and cytogenetical analysisA Shimoni, A Nagler, C Kaplinsky, et al.

Leukemia|October 14, 2006

Gene expression profiles of AML derived stem cells; similarity to hematopoietic stem cellsH Gal, N Amariglio, L Trakhtenbrot, et al.

Medical and Pediatric Oncology|February 1, 1997

Central nervous system involvement at diagnosis in a case of pediatric CD30+ anaplastic large cell lymphomaC Kaplinsky, A Toren, Y Neumann, et al.

Bone Marrow Transplantation|April 1, 1999

Successful human umbilical cord blood stem cell transplantation without conditioning in severe combined immune deficiencyA Toren, A Nagler, N Amariglio, et al.

Journal of Cell Science|October 10, 2001

Nuclear membrane protein LAP2beta mediates transcriptional repression alone and together with its binding partner GCL (germ-cell-less)E Nili, G S Cojocaru, Y Kalma, et al.

Transplantation|October 25, 2000

Amplification of immunological functions by subcutaneous injection of intermediate-high dose interleukin-2 for 2 years after autologous stem cell transplantation in children with stage IV neuroblastomaA Toren, A Nagler, G Rozenfeld-Granot, et al.

Clinical Genetics|July 4, 2015

SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosumG Heimer, D Marek-Yagel, E Eyal, et al.

Lung Cancer (Amsterdam, Netherlands)|January 30, 2007

Chromosomal aberrations and gene expression profiles in non-small cell lung cancerE Dehan, A Ben-Dor, W Liao, et al.

Journal of Medical Genetics|July 22, 2005

The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardationL Basel-Vanagaite, R Attia, M Yahav, et al.

Pageof 19