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S Wayne

Showing results (341-350 of 400) with videos related to

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Journal of Medicinal Chemistry|June 1, 2010
Synthesis and characterization of in vitro and in vivo profiles of hydroxybupropion analogues: aids to smoking cessationRonald J Lukas, Ana Z Muresan, M Imad Damaj, et al.
The Pediatric Infectious Disease Journal|February 19, 2008
Triad of severe abdominal pain, inappropriate antidiuretic hormone secretion, and disseminated varicella-zoster virus infection preceding cutaneous manifestations after hematopoietic stem cell transplantation: utility of PCR for early recognition and therapyRachel Rau, Courtney D Fitzhugh, Kristin Baird, et al.
Pediatric Blood & Cancer|July 21, 2016
Treatment-related adverse events associated with a modified UK ALLR3 induction chemotherapy backbone for childhood relapsed/refractory acute lymphoblastic leukemiaWeili Sun, Etan Orgel, Jemily Malvar, et al.
Nature Reviews. Clinical Oncology|February 26, 2021
Immunogenicity of CAR T cells in cancer therapyDimitrios L Wagner, Enrico Fritsche, Michael A Pulsipher, et al.
Blood|October 7, 2017
Phase 1 study of the anti-CD22 immunotoxin moxetumomab pasudotox for childhood acute lymphoblastic leukemiaAlan S Wayne, Nirali N Shah, Deepa Bhojwani, et al.
Human Genetics|September 12, 2000
Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairmentK Verhoeven, T Fagerheim, S Prasad, et al.
American Journal of Hematology|April 5, 2012
Myelodysplastic syndrome after allogeneic hematopoietic stem cell transplantation: diagnostic and therapeutic challengesNirali N Shah, Ulrike Bacher, Terry Fry, et al.
The Journal of Allergy and Clinical Immunology|December 14, 2011
Multicentric dermatofibrosarcoma protuberans in patients with adenosine deaminase-deficient severe combined immune deficiencyChimene Kesserwan, Robert Sokolic, Edward W Cowen, et al.
Human Molecular Genetics|June 1, 1996
A gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA10, maps to chromosome 6M E O'Neill, J Marietta, D Nishimura, et al.
American Journal of Medical Genetics|September 5, 1997
New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19pA Chen, S Wayne, A Bell, et al.
Pageof 40

Showing results (341-350 of 400) with videos related to

Sort By:
Pageof 40
Journal of Medicinal Chemistry|June 1, 2010
Synthesis and characterization of in vitro and in vivo profiles of hydroxybupropion analogues: aids to smoking cessationRonald J Lukas, Ana Z Muresan, M Imad Damaj, et al.
The Pediatric Infectious Disease Journal|February 19, 2008
Triad of severe abdominal pain, inappropriate antidiuretic hormone secretion, and disseminated varicella-zoster virus infection preceding cutaneous manifestations after hematopoietic stem cell transplantation: utility of PCR for early recognition and therapyRachel Rau, Courtney D Fitzhugh, Kristin Baird, et al.
Pediatric Blood & Cancer|July 21, 2016
Treatment-related adverse events associated with a modified UK ALLR3 induction chemotherapy backbone for childhood relapsed/refractory acute lymphoblastic leukemiaWeili Sun, Etan Orgel, Jemily Malvar, et al.
Nature Reviews. Clinical Oncology|February 26, 2021
Immunogenicity of CAR T cells in cancer therapyDimitrios L Wagner, Enrico Fritsche, Michael A Pulsipher, et al.
Blood|October 7, 2017
Phase 1 study of the anti-CD22 immunotoxin moxetumomab pasudotox for childhood acute lymphoblastic leukemiaAlan S Wayne, Nirali N Shah, Deepa Bhojwani, et al.
Human Genetics|September 12, 2000
Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairmentK Verhoeven, T Fagerheim, S Prasad, et al.
American Journal of Hematology|April 5, 2012
Myelodysplastic syndrome after allogeneic hematopoietic stem cell transplantation: diagnostic and therapeutic challengesNirali N Shah, Ulrike Bacher, Terry Fry, et al.
The Journal of Allergy and Clinical Immunology|December 14, 2011
Multicentric dermatofibrosarcoma protuberans in patients with adenosine deaminase-deficient severe combined immune deficiencyChimene Kesserwan, Robert Sokolic, Edward W Cowen, et al.
Human Molecular Genetics|June 1, 1996
A gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA10, maps to chromosome 6M E O'Neill, J Marietta, D Nishimura, et al.
American Journal of Medical Genetics|September 5, 1997
New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19pA Chen, S Wayne, A Bell, et al.
Pageof 40