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Chembiochem : a European Journal of Chemical Biology
|
August 12, 2014
Chemical interrogation of the malaria kinome
Emily R Derbyshire, Vanessa Zuzarte-Luís, Andreia D Magalhães, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 16, 2020
A nanobody targeting the LIN28:let-7 interaction fragment of TUT4 blocks uridylation of let-7
Chunxiao Yu, Longfei Wang, R Grant Rowe, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 7, 2006
Activity of dual SRC-ABL inhibitors highlights the role of BCR/ABL kinase dynamics in drug resistance
Mohammad Azam, Valentina Nardi, William C Shakespeare, et al.
The Journal of Allergy and Clinical Immunology
|
July 5, 2021
Mechanisms underlying genetic susceptibility to multisystem inflammatory syndrome in children (MIS-C)
Janet Chou, Craig D Platt, Saddiq Habiballah, et al.
Cell Reports
|
April 22, 2022
Structural and functional impact by SARS-CoV-2 Omicron spike mutations
Jun Zhang, Yongfei Cai, Christy L Lavine, et al.
Nature
|
September 21, 2018
mRNA circularization by METTL3-eIF3h enhances translation and promotes oncogenesis
Junho Choe, Shuibin Lin, Wencai Zhang, et al.
Haematologica
|
October 16, 2025
Increased percentages of circulating T follicular helper cells associate with disease subtype and activity in pediatric immune cytopenias
Emily M Harris, Aleksandra Bourdine, Logan Magin, et al.
NPJ Genomic Medicine
|
July 14, 2020
Children's rare disease cohorts: an integrative research and clinical genomics initiative
Shira Rockowitz, Nicholas LeCompte, Mary Carmack, et al.
American Journal of Hematology
|
October 22, 2021
Congenital X-linked neutropenia with myelodysplasia and somatic tetraploidy due to a germline mutation in SEPT6
Raffaele Renella, Katelyn Gagne, Ellen Beauchamp, et al.
HGG Advances
|
September 13, 2021
A data-driven architecture using natural language processing to improve phenotyping efficiency and accelerate genetic diagnoses of rare disorders
Jignesh R Parikh, Casie A Genetti, Asli Aykanat, et al.
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of 8
Search research articles
Search
Showing results (51-60 of 73) with videos related to
Sort By:
Page
of 8
Chembiochem : a European Journal of Chemical Biology
|
August 12, 2014
Chemical interrogation of the malaria kinome
Emily R Derbyshire, Vanessa Zuzarte-Luís, Andreia D Magalhães, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 16, 2020
A nanobody targeting the LIN28:let-7 interaction fragment of TUT4 blocks uridylation of let-7
Chunxiao Yu, Longfei Wang, R Grant Rowe, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 7, 2006
Activity of dual SRC-ABL inhibitors highlights the role of BCR/ABL kinase dynamics in drug resistance
Mohammad Azam, Valentina Nardi, William C Shakespeare, et al.
The Journal of Allergy and Clinical Immunology
|
July 5, 2021
Mechanisms underlying genetic susceptibility to multisystem inflammatory syndrome in children (MIS-C)
Janet Chou, Craig D Platt, Saddiq Habiballah, et al.
Cell Reports
|
April 22, 2022
Structural and functional impact by SARS-CoV-2 Omicron spike mutations
Jun Zhang, Yongfei Cai, Christy L Lavine, et al.
Nature
|
September 21, 2018
mRNA circularization by METTL3-eIF3h enhances translation and promotes oncogenesis
Junho Choe, Shuibin Lin, Wencai Zhang, et al.
Haematologica
|
October 16, 2025
Increased percentages of circulating T follicular helper cells associate with disease subtype and activity in pediatric immune cytopenias
Emily M Harris, Aleksandra Bourdine, Logan Magin, et al.
NPJ Genomic Medicine
|
July 14, 2020
Children's rare disease cohorts: an integrative research and clinical genomics initiative
Shira Rockowitz, Nicholas LeCompte, Mary Carmack, et al.
American Journal of Hematology
|
October 22, 2021
Congenital X-linked neutropenia with myelodysplasia and somatic tetraploidy due to a germline mutation in SEPT6
Raffaele Renella, Katelyn Gagne, Ellen Beauchamp, et al.
HGG Advances
|
September 13, 2021
A data-driven architecture using natural language processing to improve phenotyping efficiency and accelerate genetic diagnoses of rare disorders
Jignesh R Parikh, Casie A Genetti, Asli Aykanat, et al.
Page
of 8