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Hepatology (Baltimore, Md.)|July 29, 2021
Histone Deacetylase Sirtuin 1 Promotes Loss of Primary Cilia in CholangiocarcinomaKishor Pant, Estanislao Peixoto, Seth Richard, et al.
Blood|July 10, 2009
Identification of novel antigens with induced immune response in monoclonal gammopathy of undetermined significanceSimona Blotta, Pierfrancesco Tassone, Rao H Prabhala, et al.
American Journal of Medical Genetics. Part A|August 2, 2005
Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterization of 11 casesManuela Morleo, Tiziano Pramparo, Lucia Perone, et al.
American Journal of Medical Genetics. Part A|July 2, 2003
X-linked Opitz syndrome: novel mutations in the MID1 gene and redefinition of the clinical spectrumFrancesca De Falco, Silvia Cainarca, Grazia Andolfi, et al.
Scientific Reports|April 29, 2017
The centrosomal OFD1 protein interacts with the translation machinery and regulates the synthesis of specific targetsDaniela Iaconis, Maria Monti, Mario Renda, et al.
American Journal of Human Genetics|July 6, 2010
Terminal osseous dysplasia is caused by a single recurrent mutation in the FLNA geneYu Sun, Rowida Almomani, Emmelien Aten, et al.
Clinical and Experimental Medicine|April 10, 2024
A MiR181/Sirtuin1 regulatory circuit modulates drug response in biliary cancersAnna Barbato, Fabiola Piscopo, Massimiliano Salati, et al.
International Journal of Molecular Sciences|March 6, 2021
Integrated Genomics Identifies miR-181/TFAM Pathway as a Critical Driver of Drug Resistance in MelanomaAnna Barbato, Antonella Iuliano, Mariagrazia Volpe, et al.
EMBO Molecular Medicine|October 4, 2022
miR-181a/b downregulation: a mutation-independent therapeutic approach for inherited retinal diseasesSabrina Carrella, Martina Di Guida, Simona Brillante, et al.
European Journal of Human Genetics : EJHG|August 13, 2002
Refinement of the NHS locus on chromosome Xp22.13 and analysis of five candidate genesAnnick Toutain, Benoît Dessay, Nathalie Ronce, et al.
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