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Bone Marrow Transplantation|August 7, 2012
Long-term survival in patients with metastatic breast cancer receiving intensified chemotherapy and stem cell rescue: data from the Italian registryM Martino, A Ballestrero, A Zambelli, et al.Journal of Pharmaceutical and Biomedical Analysis|September 5, 2015
Comparison of electrospray ionization and atmospheric pressure photoionization liquid chromatography mass spectrometry methods for analysis of ergot alkaloids from endophyte-infected sleepygrass (Achnatherum robustum)Alan K Jarmusch, Ashleigh M Musso, Tatsiana Shymanovich, et al.Journal of Affective Disorders|July 10, 2012
GTP cyclohydrolase 1 gene haplotypes as predictors of SSRI response in Japanese patients with major depressive disorderTaro Kishi, Hiroshi Ichinose, Reiji Yoshimura, et al.Neuron|March 16, 2023
Subcellular mRNA localization and local translation of Arhgap11a in radial glial progenitors regulates cortical developmentLouis-Jan Pilaz, Jing Liu, Kaumudi Joshi, et al.Frontiers in Genetics|June 21, 2018
Complexity of the 5' Untranslated Region of EIF4A3, a Critical Factor for Craniofacial and Neural DevelopmentGabriella S P Hsia, Camila M Musso, Lucas Alvizi, et al.Molecular Neurobiology|November 13, 2017
Down Syndrome iPSC-Derived Astrocytes Impair Neuronal Synaptogenesis and the mTOR Pathway In VitroBruno H S Araujo, Carolini Kaid, Janaina S De Souza, et al.Bone Marrow Transplantation|November 12, 2014
Onset and outcome of pregnancy after autologous haematopoietic SCT (AHSCT) for autoimmune diseases: a retrospective study of the EBMT autoimmune diseases working party (ADWP)E Snarski, J A Snowden, M C Oliveira, et al.Biorxiv : the Preprint Server for Biology|April 22, 2024
A human-specific enhancer fine-tunes radial glia potency and corticogenesisJing Liu, Federica Mosti, Hanzhi T Zhao, et al.Clinical Genetics|June 29, 2016
Impact of rare variants in ARHGAP29 to the etiology of oral clefts: role of loss-of-function vs missense variantsC P Savastano, L A Brito, Á C Faria, et al.Human Molecular Genetics|March 24, 2017
EIF4A3 deficient human iPSCs and mouse models demonstrate neural crest defects that underlie Richieri-Costa-Pereira syndromeEmily E Miller, Gerson S Kobayashi, Camila M Musso, et al.Pageof 12