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Hemoglobin

Showing results (431-440 of 3,216) with videos related to

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Hemoglobin|December 19, 2018
The Chaperones Involved in Hemoglobin Synthesis Take the Spotlight: Analysis of AHSP in the Argentinean Population and Review of the LiteratureKaren G Scheps, Viviana Varela, Héctor M Targovnik
Hemoglobin|January 5, 2020
Association between Different Polymorphic Markers and β-Thalassemia Intermedia in Central IranZahra Sajadpour, Zeinab Amini-Farsani, Majid Motovali-Bashi, et al.
Hemoglobin|January 25, 2020
An Unusual Compound Heterozygosity for Hb O-Arab (<i>HBB</i>: c.364G>A) and Hb D-Los Angeles (<i>HBB</i>: c.364G>C)Adriaan J van Gammeren, Leonie Pelkmans, Corné C W van Endschot, et al.
Hemoglobin|October 29, 2019
A Kindred with a β-Globin Base Substitution [β89(F5)Ser→Arg (AG<i>T</i>>AG<i>G</i>); <i>HBB</i>: c.270T>G] Resulting in Hemoglobin VanderbiltWilliam Shomali, Rondeep Brar, Subramanyeswara R Arekapudi, et al.
Hemoglobin|January 1, 1992
The IVS-I-110 (G-->T) and codon 39 (C-->T) beta-thalassemia mutations in association with alpha-thal-2 (-3.7 Kb) and Hb Hasharon [alpha 47(CE5)Asp-->His] in a Brazilian patientF F Costa, M S Figueredo, M F Sonati, et al.
Hemoglobin|January 1, 1992
Hemoglobinopathies in Yugoslavia: an updateG D Efremov
Hemoglobin|January 1, 1992
Mild Hb Constant Spring-Hb H disease with beta zero-thalassemia traitX J Wen, S Liang
Hemoglobin|January 1, 1992
Hemoglobinopathies in SardiniaB Masala
Hemoglobin|June 1, 2005
Molecular and clinical features of Hb H disease in northern ThailandPimlak Charoenkwan, Rawee Taweephon, Rattika Sae-Tung, et al.
Hemoglobin|June 1, 2005
ATR-16 due to a de novo complex rearrangement of chromosome 16Marta S Gallego, Gabriela Zelaya, Aurora S Feliu, et al.
Pageof 322

Showing results (431-440 of 3,216) with videos related to

Sort By:
Pageof 322
Hemoglobin|December 19, 2018
The Chaperones Involved in Hemoglobin Synthesis Take the Spotlight: Analysis of AHSP in the Argentinean Population and Review of the LiteratureKaren G Scheps, Viviana Varela, Héctor M Targovnik
Hemoglobin|January 5, 2020
Association between Different Polymorphic Markers and β-Thalassemia Intermedia in Central IranZahra Sajadpour, Zeinab Amini-Farsani, Majid Motovali-Bashi, et al.
Hemoglobin|January 25, 2020
An Unusual Compound Heterozygosity for Hb O-Arab (<i>HBB</i>: c.364G>A) and Hb D-Los Angeles (<i>HBB</i>: c.364G>C)Adriaan J van Gammeren, Leonie Pelkmans, Corné C W van Endschot, et al.
Hemoglobin|October 29, 2019
A Kindred with a β-Globin Base Substitution [β89(F5)Ser→Arg (AG<i>T</i>>AG<i>G</i>); <i>HBB</i>: c.270T>G] Resulting in Hemoglobin VanderbiltWilliam Shomali, Rondeep Brar, Subramanyeswara R Arekapudi, et al.
Hemoglobin|January 1, 1992
The IVS-I-110 (G-->T) and codon 39 (C-->T) beta-thalassemia mutations in association with alpha-thal-2 (-3.7 Kb) and Hb Hasharon [alpha 47(CE5)Asp-->His] in a Brazilian patientF F Costa, M S Figueredo, M F Sonati, et al.
Hemoglobin|January 1, 1992
Hemoglobinopathies in Yugoslavia: an updateG D Efremov
Hemoglobin|January 1, 1992
Mild Hb Constant Spring-Hb H disease with beta zero-thalassemia traitX J Wen, S Liang
Hemoglobin|January 1, 1992
Hemoglobinopathies in SardiniaB Masala
Hemoglobin|June 1, 2005
Molecular and clinical features of Hb H disease in northern ThailandPimlak Charoenkwan, Rawee Taweephon, Rattika Sae-Tung, et al.
Hemoglobin|June 1, 2005
ATR-16 due to a de novo complex rearrangement of chromosome 16Marta S Gallego, Gabriela Zelaya, Aurora S Feliu, et al.
Pageof 322