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Annals of Oncology : Official Journal of the European Society for Medical Oncology|October 19, 2017
SELECT-2: a phase II, double-blind, randomized, placebo-controlled study to assess the efficacy of selumetinib plus docetaxel as a second-line treatment of patients with advanced or metastatic non-small-cell lung cancerJ-C Soria, A Fülöp, C Maciel, et al.Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|August 17, 2004
Craniopagus: the Suriname-Amsterdam conjunctionW J R van Ouwerkerk, R van den Berg, C E Allison, et al.The New Phytologist|February 23, 2018
Lost in diversity: the interactions between soil-borne fungi, biodiversity and plant productivityLiesje Mommer, T E Anne Cotton, Jos M Raaijmakers, et al.Cephalalgia : an International Journal of Headache|April 10, 2016
Cerebellar function and ischemic brain lesions in migraine patients from the general populationHille Koppen, Henk-Jan Boele, Inge H Palm-Meinders, et al.Journal of Child and Adolescent Psychopharmacology|December 29, 2009
Differential effects of atomoxetine on executive functioning and lexical decision in attention-deficit/hyperactivity disorder and reading disorderChristien G W de Jong, Séverine Van De Voorde, Herbert Roeyers, et al.Nature|November 19, 2020
A network of transcriptional repressors modulates auxin responsesJekaterina Truskina, Jingyi Han, Elina Chrysanthou, et al.Blood|October 24, 2002
High EVI1 expression predicts poor survival in acute myeloid leukemia: a study of 319 de novo AML patientsSahar Barjesteh van Waalwijk van Doorn-Khosrovani, Claudia Erpelinck, Wim L J van Putten, et al.Neuron|August 2, 2005
Deletion of FMR1 in Purkinje cells enhances parallel fiber LTD, enlarges spines, and attenuates cerebellar eyelid conditioning in Fragile X syndromeS K E Koekkoek, K Yamaguchi, B A Milojkovic, et al.JACC. Advances|January 16, 2025
Etiology and Phenotypes of Cardiomyopathy in Southern Africa: The IMHOTEP Multicenter Pilot StudySarah M Kraus, Jacqui Cirota, Shahiemah Pandie, et al.American Journal of Human Genetics|July 9, 2016
Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis PigmentosaAndrea Angius, Paolo Uva, Insa Buers, et al.Pageof 47