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The Journal of Investigative Dermatology
|
August 14, 2020
Distribution and Functional Consequences of Somatic MAP2K1 Variants in Affected Skin Associated with Bone Lesions in Melorheostosis
Smita Jha, Aleksandra Ivovic, Heeseog Kang, et al.
Oncotarget
|
May 10, 2014
Anti-vascular endothelial growth factor therapy-induced glioma invasion is associated with accumulation of Tie2-expressing monocytes
Konrad Gabrusiewicz, Dan Liu, Nahir Cortes-Santiago, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease
|
May 6, 2019
COL1A1 C-propeptide mutations cause ER mislocalization of procollagen and impair C-terminal procollagen processing
Aileen M Barnes, Aarthi Ashok, Elena N Makareeva, et al.
Blood
|
November 11, 2010
Targeting neuropilin-1 in human leukemia and lymphoma
Katja Karjalainen, Diana E Jaalouk, Carlos E Bueso-Ramos, et al.
Bone
|
September 1, 2019
Bruck syndrome 2 variant lacking congenital contractures and involving a novel compound heterozygous PLOD2 mutation
Steven Mumm, Gary S Gottesman, Deborah Wenkert, et al.
Human Mutation
|
May 29, 2013
Kuskokwim syndrome, a recessive congenital contracture disorder, extends the phenotype of FKBP10 mutations
Aileen M Barnes, Geraldine Duncan, Maryann Weis, et al.
BMC Genomics
|
July 7, 2007
Transcriptome profiling of the small intestinal epithelium in germfree versus conventional piglets
Shankar R Chowdhury, Dale E King, Benjamin P Willing, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 8, 2016
Non-Lethal Type VIII Osteogenesis Imperfecta Has Elevated Bone Matrix Mineralization
Nadja Fratzl-Zelman, Aileen M Barnes, MaryAnn Weis, et al.
Plos One
|
December 7, 2013
Human omental-derived adipose stem cells increase ovarian cancer proliferation, migration, and chemoresistance
Aleksandra Nowicka, Frank C Marini, Travis N Solley, et al.
Nature Communications
|
April 13, 2018
Somatic activating mutations in MAP2K1 cause melorheostosis
Heeseog Kang, Smita Jha, Zuoming Deng, et al.
Page
of 86
Search research articles
Search
Showing results (511-520 of 852) with videos related to
Sort By:
Page
of 86
The Journal of Investigative Dermatology
|
August 14, 2020
Distribution and Functional Consequences of Somatic MAP2K1 Variants in Affected Skin Associated with Bone Lesions in Melorheostosis
Smita Jha, Aleksandra Ivovic, Heeseog Kang, et al.
Oncotarget
|
May 10, 2014
Anti-vascular endothelial growth factor therapy-induced glioma invasion is associated with accumulation of Tie2-expressing monocytes
Konrad Gabrusiewicz, Dan Liu, Nahir Cortes-Santiago, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease
|
May 6, 2019
COL1A1 C-propeptide mutations cause ER mislocalization of procollagen and impair C-terminal procollagen processing
Aileen M Barnes, Aarthi Ashok, Elena N Makareeva, et al.
Blood
|
November 11, 2010
Targeting neuropilin-1 in human leukemia and lymphoma
Katja Karjalainen, Diana E Jaalouk, Carlos E Bueso-Ramos, et al.
Bone
|
September 1, 2019
Bruck syndrome 2 variant lacking congenital contractures and involving a novel compound heterozygous PLOD2 mutation
Steven Mumm, Gary S Gottesman, Deborah Wenkert, et al.
Human Mutation
|
May 29, 2013
Kuskokwim syndrome, a recessive congenital contracture disorder, extends the phenotype of FKBP10 mutations
Aileen M Barnes, Geraldine Duncan, Maryann Weis, et al.
BMC Genomics
|
July 7, 2007
Transcriptome profiling of the small intestinal epithelium in germfree versus conventional piglets
Shankar R Chowdhury, Dale E King, Benjamin P Willing, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 8, 2016
Non-Lethal Type VIII Osteogenesis Imperfecta Has Elevated Bone Matrix Mineralization
Nadja Fratzl-Zelman, Aileen M Barnes, MaryAnn Weis, et al.
Plos One
|
December 7, 2013
Human omental-derived adipose stem cells increase ovarian cancer proliferation, migration, and chemoresistance
Aleksandra Nowicka, Frank C Marini, Travis N Solley, et al.
Nature Communications
|
April 13, 2018
Somatic activating mutations in MAP2K1 cause melorheostosis
Heeseog Kang, Smita Jha, Zuoming Deng, et al.
Page
of 86