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Investigation of the 2f(1)-f(2) and 2f(2)-f(1) distortion product otoacoustic emissions using a computational

Investigation of the anomalously low B(E2; 4(1)(+) -> 2(1)(+))/B(E2; 2(1)(+) -> 0(1)(+)) ratio in Ce-

REPRESENTATION OF 1/2 (F-n - 1)(Fn+1 - 1) AND 1/2 (F-n - 1)(Fn+2 - 1)

Examining the Factors that Contribute to Non-Monotonic Growth of the 2f(1) - f(2) Otoacoustic Emission

Analysis of Level Dependence of 2f(1) - f(2) Component of Otoacoustic Emissions Using Nonlinear 2D Cochlear

B-d,s(0) -> f(1)f(1 )decays with f(1) (1285) - f(1) (1420) mixing in the perturbative QCD approach

Calcitriol Suppresses HIF-1 and HIF-2 Transcriptional Activity by Reducing HIF-1/2 alpha Protein Levels

Hadronic weak decay B-b(1/2(+)) -> B(1/2(+),3/2(+)) + V

On a Generalization of Kummer's Second-Type F-1(1) and F-2(2)

F (1) F (2)-selective NMR spectroscopy

NF-kappa B1 p50 stabilizes HIF-1 alpha protein through suppression of ATG7-dependent autophagy

One Ce, Two Ce, Three Ce, Four? An Intermetallic Homologous Series to Explore: A(n+1)B(n)X(3n+1)

A collective description of the unusually low ratio B-4/2 = B(E2; 4(1)(+) -> 2(1)(+))/B(E2; 2(1)(+) -> 0(1)(+))

Genus 2 Lefschetz fibrations with b(2)(+)=1 and c(1)(2)=1, 2

Upregulation of COX4-2 via HIF-1 alpha in Mitochondrial COX4-1 Deficiency

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