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Journal of Medicinal Chemistry
|
June 20, 1997
Pyridazinodiazepines as a high-affinity, P2-P3 peptidomimetic class of interleukin-1 beta-converting enzyme inhibitor
R E Dolle, C V Prasad, C P Prouty, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
September 1, 2019
Hybridization capture-based next generation sequencing reliably detects FLT3 mutations and classifies FLT3-internal tandem duplication allelic ratio in acute myeloid leukemia: a comparative study to standard fragment analysis
Rong He, Daniel J Devine, Zheng Jin Tu, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
October 9, 2019
Correction to: Hybridization capture-based next-generation sequencing reliably detects FLT3 mutations and classifies FLT3-internal tandem duplication allelic ratio in acute myeloid leukemia: a comparative study to standard fragment analysis
Rong He, Daniel J Devine, Zheng Jin Tu, et al.
Mayo Clinic Proceedings
|
April 29, 1998
Hemoglobin Old Dominion/Burton-upon-Trent, beta 143 (H21) His-->Tyr, codon 143 CAC-->TAC--a variant with altered oxygen affinity that compromises measurement of glycated hemoglobin in diabetes mellitus: structure, function, and DNA sequence
G E Elder, T R Lappin, A B Horne, et al.
American Journal of Hematology
|
October 26, 2018
Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiency
Paola Bianchi, Elisa Fermo, Bertil Glader, et al.
American Journal of Clinical Pathology
|
May 12, 2021
Pathologic Spectrum and Molecular Landscape of Myeloid Disorders Harboring SF3B1 Mutations
Elise R Venable, Dong Chen, Constance P Chen, et al.
The Journal of Molecular Diagnostics : JMD
|
November 29, 2021
Improved Characterization of Complex β-Globin Gene Cluster Structural Variants Using Long-Read Sequencing
Aruna Rangan, Molly S Hein, William G Jenkinson, et al.
Blood Cancer Journal
|
January 26, 2022
Molecular markers demonstrate diagnostic and prognostic value in the evaluation of myelodysplastic syndromes in cytopenia patients
Rong He, Jonathan Chiou, Allison Chiou, et al.
Nature Genetics
|
March 23, 2011
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach
Belinda Giardine, Joseph Borg, Douglas R Higgs, et al.
HGG Advances
|
February 24, 2022
First genome-wide association study of esophageal atresia identifies three genetic risk loci at <i>CTNNA3</i>, <i>FOXF1</i>/<i>FOXC2</i>/<i>FOXL1</i>, and <i>HNF1B</i>
Jan Gehlen, Ann-Sophie Giel, Ricarda Köllges, et al.
Page
of 40
Search research articles
Search
Showing results (381-390 of 391) with videos related to
Sort By:
Page
of 40
Journal of Medicinal Chemistry
|
June 20, 1997
Pyridazinodiazepines as a high-affinity, P2-P3 peptidomimetic class of interleukin-1 beta-converting enzyme inhibitor
R E Dolle, C V Prasad, C P Prouty, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
September 1, 2019
Hybridization capture-based next generation sequencing reliably detects FLT3 mutations and classifies FLT3-internal tandem duplication allelic ratio in acute myeloid leukemia: a comparative study to standard fragment analysis
Rong He, Daniel J Devine, Zheng Jin Tu, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
October 9, 2019
Correction to: Hybridization capture-based next-generation sequencing reliably detects FLT3 mutations and classifies FLT3-internal tandem duplication allelic ratio in acute myeloid leukemia: a comparative study to standard fragment analysis
Rong He, Daniel J Devine, Zheng Jin Tu, et al.
Mayo Clinic Proceedings
|
April 29, 1998
Hemoglobin Old Dominion/Burton-upon-Trent, beta 143 (H21) His-->Tyr, codon 143 CAC-->TAC--a variant with altered oxygen affinity that compromises measurement of glycated hemoglobin in diabetes mellitus: structure, function, and DNA sequence
G E Elder, T R Lappin, A B Horne, et al.
American Journal of Hematology
|
October 26, 2018
Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiency
Paola Bianchi, Elisa Fermo, Bertil Glader, et al.
American Journal of Clinical Pathology
|
May 12, 2021
Pathologic Spectrum and Molecular Landscape of Myeloid Disorders Harboring SF3B1 Mutations
Elise R Venable, Dong Chen, Constance P Chen, et al.
The Journal of Molecular Diagnostics : JMD
|
November 29, 2021
Improved Characterization of Complex β-Globin Gene Cluster Structural Variants Using Long-Read Sequencing
Aruna Rangan, Molly S Hein, William G Jenkinson, et al.
Blood Cancer Journal
|
January 26, 2022
Molecular markers demonstrate diagnostic and prognostic value in the evaluation of myelodysplastic syndromes in cytopenia patients
Rong He, Jonathan Chiou, Allison Chiou, et al.
Nature Genetics
|
March 23, 2011
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach
Belinda Giardine, Joseph Borg, Douglas R Higgs, et al.
HGG Advances
|
February 24, 2022
First genome-wide association study of esophageal atresia identifies three genetic risk loci at <i>CTNNA3</i>, <i>FOXF1</i>/<i>FOXC2</i>/<i>FOXL1</i>, and <i>HNF1B</i>
Jan Gehlen, Ann-Sophie Giel, Ricarda Köllges, et al.
Page
of 40