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Journal of Molecular Medicine (Berlin, Germany)
|
September 18, 2021
The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotype
Luisa Averdunk, Heinrich Sticht, Harald Surowy, et al.
Neuro-Oncology
|
September 1, 2016
Long-term survival in AIDS-related primary central nervous system lymphoma
Neel K Gupta, Amber Nolan, Antonio Omuro, et al.
Cell Host & Microbe
|
May 15, 2015
The Toxoplasma Dense Granule Proteins GRA17 and GRA23 Mediate the Movement of Small Molecules between the Host and the Parasitophorous Vacuole
Daniel A Gold, Aaron D Kaplan, Agnieszka Lis, et al.
Cell
|
August 13, 2013
From structure to systems: high-resolution, quantitative genetic analysis of RNA polymerase II
Hannes Braberg, Huiyan Jin, Erica A Moehle, et al.
American Journal of Hematology
|
March 15, 2020
Bortezomib consolidation or maintenance following immunochemotherapy and autologous stem cell transplantation for mantle cell lymphoma: CALGB/Alliance 50403
Lawrence D Kaplan, Matthew J Maurer, Wendy Stock, et al.
Genome Biology
|
June 4, 2020
Universal promoter scanning by Pol II during transcription initiation in Saccharomyces cerevisiae
Chenxi Qiu, Huiyan Jin, Irina Vvedenskaya, et al.
Blood
|
December 22, 2009
Rituximab plus concurrent infusional EPOCH chemotherapy is highly effective in HIV-associated B-cell non-Hodgkin lymphoma
Joseph A Sparano, Jeannette Y Lee, Lawrence D Kaplan, et al.
Science Signaling
|
December 9, 2025
The scavenger receptor MARCO is a ligand for the immune inhibitory receptor LAIR-1 and regulates its function in cis
Akashdip Singh, Saskia V Vijver, Hajar Aglmous-Talibi, et al.
European Journal of Human Genetics : EJHG
|
February 17, 2021
Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3-a subgroup of K<sup>+</sup> channelopathies
Karen W Gripp, Sarah F Smithson, Ingrid J Scurr, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 22, 2020
Expanding the clinical and genetic spectrum of CAD deficiency: an epileptic encephalopathy treatable with uridine supplementation
Daisy Rymen, Martijn Lindhout, Maria Spanou, et al.
Page
of 87
Search research articles
Search
Showing results (811-820 of 861) with videos related to
Sort By:
Page
of 87
Journal of Molecular Medicine (Berlin, Germany)
|
September 18, 2021
The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotype
Luisa Averdunk, Heinrich Sticht, Harald Surowy, et al.
Neuro-Oncology
|
September 1, 2016
Long-term survival in AIDS-related primary central nervous system lymphoma
Neel K Gupta, Amber Nolan, Antonio Omuro, et al.
Cell Host & Microbe
|
May 15, 2015
The Toxoplasma Dense Granule Proteins GRA17 and GRA23 Mediate the Movement of Small Molecules between the Host and the Parasitophorous Vacuole
Daniel A Gold, Aaron D Kaplan, Agnieszka Lis, et al.
Cell
|
August 13, 2013
From structure to systems: high-resolution, quantitative genetic analysis of RNA polymerase II
Hannes Braberg, Huiyan Jin, Erica A Moehle, et al.
American Journal of Hematology
|
March 15, 2020
Bortezomib consolidation or maintenance following immunochemotherapy and autologous stem cell transplantation for mantle cell lymphoma: CALGB/Alliance 50403
Lawrence D Kaplan, Matthew J Maurer, Wendy Stock, et al.
Genome Biology
|
June 4, 2020
Universal promoter scanning by Pol II during transcription initiation in Saccharomyces cerevisiae
Chenxi Qiu, Huiyan Jin, Irina Vvedenskaya, et al.
Blood
|
December 22, 2009
Rituximab plus concurrent infusional EPOCH chemotherapy is highly effective in HIV-associated B-cell non-Hodgkin lymphoma
Joseph A Sparano, Jeannette Y Lee, Lawrence D Kaplan, et al.
Science Signaling
|
December 9, 2025
The scavenger receptor MARCO is a ligand for the immune inhibitory receptor LAIR-1 and regulates its function in cis
Akashdip Singh, Saskia V Vijver, Hajar Aglmous-Talibi, et al.
European Journal of Human Genetics : EJHG
|
February 17, 2021
Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3-a subgroup of K<sup>+</sup> channelopathies
Karen W Gripp, Sarah F Smithson, Ingrid J Scurr, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 22, 2020
Expanding the clinical and genetic spectrum of CAD deficiency: an epileptic encephalopathy treatable with uridine supplementation
Daisy Rymen, Martijn Lindhout, Maria Spanou, et al.
Page
of 87