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D Hoyer

Showing results (181-190 of 391) with videos related to

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British Journal of Haematology|December 21, 2004
Peripheral blood CD34 count in myelofibrosis with myeloid metaplasia: a prospective evaluation of prognostic value in 94 patientsBrijesh Arora, Shireen Sirhan, James D Hoyer, et al.
Pediatrics|August 3, 2004
Hyperbilirubinemia among African American, glucose-6-phosphate dehydrogenase-deficient neonatesMichael Kaplan, Marguerite Herschel, Cathy Hammerman, et al.
Conference Proceedings : ... Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual Conference|February 3, 2007
Evaluation of different rhythms by hidden Markov models in heart rate variability of hypertrophic cardiomyopathy patientsM Vallverdú, M Palacios, D Hoyer, et al.
Pneumologie (Stuttgart, Germany)|April 1, 1997
[Deterministic-chaotic and spectral-functional analysis of heart rate and respiratory movements]U Zwiener, D Hoyer, R Bauer, et al.
Hemoglobin|July 3, 2014
β-Thalassemia major resulting from compound heterozygosity for HBB: c.92+2T>C [formerly known as IVS-I-2 (T>C)] and a novel β(0)-thalassemia frameshift mutation: HBB: c.209delG; p.Gly70Valfs*20Michelle L Kluge, James D Hoyer, Kenneth C Swanson, et al.
Journal of Neurochemistry|April 2, 1998
Distinct changes in peptide YY binding to, and mRNA levels of, Y1 and Y2 receptors in the rat hippocampus associated with kindling epileptogenesisM Gobbi, M Gariboldi, C Piwko, et al.
Neuroscience Letters|May 16, 1988
Visualization of a novel serotonin recognition site (5-HT1D) in the human brain by autoradiographyC Waeber, M M Dietl, D Hoyer, et al.
British Journal of Haematology|August 25, 1999
Isolated isochromosome 17q: a distinct type of mixed myeloproliferative disorder/myelodysplastic syndrome with an aggressive clinical courseR F McClure, G W Dewald, J D Hoyer, et al.
European Journal of Pharmacology|August 31, 2001
Lack of evidence for cross-competition between vasoactive intestinal peptide and somatostatin at their respective receptorsJ P Hannon, D Langenegger, B Waser, et al.
Hemoglobin|January 22, 2011
Hb Nebraska [β86(F2)Ala→Ile (HBB:c.259G>A;260C>T)]: a unique high oxygen affinity hemoglobin variant with a double nucleotide substitution within the same codonJames D Hoyer, Patricia C Wendt, William J Hogan, et al.
Pageof 40

Showing results (181-190 of 391) with videos related to

Sort By:
Pageof 40
British Journal of Haematology|December 21, 2004
Peripheral blood CD34 count in myelofibrosis with myeloid metaplasia: a prospective evaluation of prognostic value in 94 patientsBrijesh Arora, Shireen Sirhan, James D Hoyer, et al.
Pediatrics|August 3, 2004
Hyperbilirubinemia among African American, glucose-6-phosphate dehydrogenase-deficient neonatesMichael Kaplan, Marguerite Herschel, Cathy Hammerman, et al.
Conference Proceedings : ... Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual Conference|February 3, 2007
Evaluation of different rhythms by hidden Markov models in heart rate variability of hypertrophic cardiomyopathy patientsM Vallverdú, M Palacios, D Hoyer, et al.
Pneumologie (Stuttgart, Germany)|April 1, 1997
[Deterministic-chaotic and spectral-functional analysis of heart rate and respiratory movements]U Zwiener, D Hoyer, R Bauer, et al.
Hemoglobin|July 3, 2014
β-Thalassemia major resulting from compound heterozygosity for HBB: c.92+2T>C [formerly known as IVS-I-2 (T>C)] and a novel β(0)-thalassemia frameshift mutation: HBB: c.209delG; p.Gly70Valfs*20Michelle L Kluge, James D Hoyer, Kenneth C Swanson, et al.
Journal of Neurochemistry|April 2, 1998
Distinct changes in peptide YY binding to, and mRNA levels of, Y1 and Y2 receptors in the rat hippocampus associated with kindling epileptogenesisM Gobbi, M Gariboldi, C Piwko, et al.
Neuroscience Letters|May 16, 1988
Visualization of a novel serotonin recognition site (5-HT1D) in the human brain by autoradiographyC Waeber, M M Dietl, D Hoyer, et al.
British Journal of Haematology|August 25, 1999
Isolated isochromosome 17q: a distinct type of mixed myeloproliferative disorder/myelodysplastic syndrome with an aggressive clinical courseR F McClure, G W Dewald, J D Hoyer, et al.
European Journal of Pharmacology|August 31, 2001
Lack of evidence for cross-competition between vasoactive intestinal peptide and somatostatin at their respective receptorsJ P Hannon, D Langenegger, B Waser, et al.
Hemoglobin|January 22, 2011
Hb Nebraska [β86(F2)Ala→Ile (HBB:c.259G>A;260C>T)]: a unique high oxygen affinity hemoglobin variant with a double nucleotide substitution within the same codonJames D Hoyer, Patricia C Wendt, William J Hogan, et al.
Pageof 40