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Journal of Medical Genetics
|
June 15, 2010
Clinical characterisation of 29 neurofibromatosis type-1 patients with molecularly ascertained 1.4 Mb type-1 NF1 deletions
V-F Mautner, L Kluwe, R E Friedrich, et al.
Science Advances
|
June 1, 2023
Lineage-specific accelerated sequences underlying primate evolution
Xupeng Bi, Long Zhou, Jin-Jin Zhang, et al.
Leukemia
|
October 19, 2011
Short telomeres result in chromosomal instability in hematopoietic cells and precede malignant evolution in human aplastic anemia
R T Calado, J N Cooper, H M Padilla-Nash, et al.
Human Genetics
|
February 24, 2001
Human type I hair keratin pseudogene phihHaA has functional orthologs in the chimpanzee and gorilla: evidence for recent inactivation of the human gene after the Pan-Homo divergence
H Winter, L Langbein, M Krawczak, et al.
Human Mutation
|
February 1, 2011
Mosaic type-1 NF1 microdeletions as a cause of both generalized and segmental neurofibromatosis type-1 (NF1)
Ludwine Messiaen, Julia Vogt, Kathrin Bengesser, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
February 5, 2013
Growth and activation of natural killer cells ex vivo from children with neuroblastoma for adoptive cell therapy
Yin Liu, Hong-Wei Wu, Michael A Sheard, et al.
Plos One
|
February 11, 2020
Very rapid cloning, expression and identifying specificity of T-cell receptors for T-cell engineering
Shan Zong, Tiejuan Mi, Leo G Flores, et al.
Plos One
|
December 20, 2018
The sequencing and interpretation of the genome obtained from a Serbian individual
Wazim Mohammed Ismail, Kymberleigh A Pagel, Vikas Pejaver, et al.
The Journal of Extra-Corporeal Technology
|
September 12, 2015
Hemolysis-Associated Nitric Oxide Dysregulation during Extracorporeal Membrane Oxygenation
Jason P Sulkowski, Jennifer N Cooper, Erik G Pearson, et al.
Journal of Clinical Pathology
|
November 29, 2005
Postmortem diagnosis of chronic granulomatous disease: how worthwhile is it?
R Lakshman, S Bruce, D A Spencer, et al.
Page
of 122
Search research articles
Search
Showing results (771-780 of 1,219) with videos related to
Sort By:
Page
of 122
Journal of Medical Genetics
|
June 15, 2010
Clinical characterisation of 29 neurofibromatosis type-1 patients with molecularly ascertained 1.4 Mb type-1 NF1 deletions
V-F Mautner, L Kluwe, R E Friedrich, et al.
Science Advances
|
June 1, 2023
Lineage-specific accelerated sequences underlying primate evolution
Xupeng Bi, Long Zhou, Jin-Jin Zhang, et al.
Leukemia
|
October 19, 2011
Short telomeres result in chromosomal instability in hematopoietic cells and precede malignant evolution in human aplastic anemia
R T Calado, J N Cooper, H M Padilla-Nash, et al.
Human Genetics
|
February 24, 2001
Human type I hair keratin pseudogene phihHaA has functional orthologs in the chimpanzee and gorilla: evidence for recent inactivation of the human gene after the Pan-Homo divergence
H Winter, L Langbein, M Krawczak, et al.
Human Mutation
|
February 1, 2011
Mosaic type-1 NF1 microdeletions as a cause of both generalized and segmental neurofibromatosis type-1 (NF1)
Ludwine Messiaen, Julia Vogt, Kathrin Bengesser, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
February 5, 2013
Growth and activation of natural killer cells ex vivo from children with neuroblastoma for adoptive cell therapy
Yin Liu, Hong-Wei Wu, Michael A Sheard, et al.
Plos One
|
February 11, 2020
Very rapid cloning, expression and identifying specificity of T-cell receptors for T-cell engineering
Shan Zong, Tiejuan Mi, Leo G Flores, et al.
Plos One
|
December 20, 2018
The sequencing and interpretation of the genome obtained from a Serbian individual
Wazim Mohammed Ismail, Kymberleigh A Pagel, Vikas Pejaver, et al.
The Journal of Extra-Corporeal Technology
|
September 12, 2015
Hemolysis-Associated Nitric Oxide Dysregulation during Extracorporeal Membrane Oxygenation
Jason P Sulkowski, Jennifer N Cooper, Erik G Pearson, et al.
Journal of Clinical Pathology
|
November 29, 2005
Postmortem diagnosis of chronic granulomatous disease: how worthwhile is it?
R Lakshman, S Bruce, D A Spencer, et al.
Page
of 122