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Nature Genetics|January 10, 2017
SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndromeNatalie D Shaw, Harrison Brand, Zachary A Kupchinsky, et al.Euphytica: Netherlands Journal of Plant Breeding|June 13, 2019
Correction to: Strategic crossing of biomass and harvest index-source and sink-achieves genetic gains in wheatMatthew P Reynolds, Alistair J D Pask, William J E Hoppitt, et al.Human Molecular Genetics|January 10, 2014
Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritanceFrank J Kaiser, Morad Ansari, Diana Braunholz, et al.Nature Genetics|April 8, 2026
Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changesRocio Rius, Alexander J M Blakes, Yuyang Chen, et al.Physical Review Letters|March 25, 2014
First results from the LUX dark matter experiment at the Sanford underground research facilityD S Akerib, H M Araújo, X Bai, et al.Physical Review Letters|February 28, 2025
Nuclear Recoil Calibration at Sub-keV Energies in LUX and Its Impact on Dark Matter Search SensitivityD S Akerib, S Alsum, H M Araújo, et al.Science (New York, N.Y.)|December 23, 2021
Dietary fiber and probiotics influence the gut microbiome and melanoma immunotherapy responseChristine N Spencer, Jennifer L McQuade, Vancheswaran Gopalakrishnan, et al.World Journal of Emergency Surgery : WJES|May 11, 2023
The unrestricted global effort to complete the COOL trialAndrew W Kirkpatrick, Federico Coccolini, Matti Tolonen, et al.Physical Review Letters|July 12, 2017
Limits on Spin-Dependent WIMP-Nucleon Cross Section Obtained from the Complete LUX ExposureD S Akerib, S Alsum, H M Araújo, et al.Physical Review Letters|April 24, 2019
Results of a Search for Sub-GeV Dark Matter Using 2013 LUX DataD S Akerib, S Alsum, H M Araújo, et al.Pageof 212