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Protein-serine-threonine kinases/genetics
 
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 TitleAuthors / EditorsDate
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 Activity-dependent regulation of genes implicated in X-linked non-specific mental retardation Boda, Bernadett; Mas, Christophe; Muller, Dominique 2002
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 Search for the second Peutz-Jeghers syndrome locus: exclusion of the STK13, PRKCG, KLK10, and PSCD2 genes on chromosome 19 and the STK11IP gene on chromosome 2 Buchet-Poyau, K.; Mehenni, H.; Radhakrishna, U.; Antonarakis, Stylianos 2002
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 ATM gene alterations in childhood acute lymphoblastic leukemias Gumy Pause, Fabienne; Wacker, Pierre; Maillet, Philippe; Betts, David; Sappino, Pascal 2003
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 ATM gene and lymphoid malignancies Gumy Pause, Fabienne; Wacker, Pierre; Sappino, Pascal 2004
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 ATM alterations in childhood non-Hodgkin lymphoma Gumy Pause, Fabienne; Wacker, Pierre; Maillet, Philippe; Betts, David R; Sappino, Pascal 2006
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 ATM promoter analysis in childhood lymphoid malignancies: a brief communication Gumy Pause, Fabienne; Wacker, Pierre; Maillet, Philippe; Betts, David R; Sappino, Pascal 2006
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 ATM variants and predisposition to childhood T-lineage acute lymphoblastic leukaemia Gumy Pause, Fabienne; Wacker, Pierre; Maillet, Philippe; Betts, D R; Sappino, Pascal 2006
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 Molecular and clinical characteristics in 46 families affected with Peutz-Jeghers syndrome Mehenni, Hamid; Resta, Nicoletta; Guanti, Ginevra; Mota-Vieira, Louisa; ... Picard, Didier 2007
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 PR-Set7-dependent lysine methylation ensures genome replication and stability through S phase Tardat, Mathieu; Murr, Rabih; Herceg, Zdenko; Sardet, Claude; Julien, Eric 2007
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 Evolutionary appearance of mononucleotide repeats in the coding sequences of four genes in primates Giacobino, Ariane; Chaillet, John Richard 2007
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 Detection of ATM gene deletion/duplication by multiplex ligation-dependant probe amplification in childhood lymphoid malignancies: a report from the Children's Oncology Group Gumy Pause, Fabienne; Ozsahin, Ayse Hulya; Khoshbeen-Boudal, Mary; Betts, David R.; ... Sappino, Pascal 2008
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 Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's disease Lesage, S; Condroyer, C; Lannuzel, A; Lohmann, E; ... Brice, A 2009
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 Low disease risk in relatives of north african lrrk2 Parkinson disease patients Troiano, A R; Elbaz, A; Lohmann, E; Belarbi, S; ... Brice, A 2010
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 Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans Lesage, Suzanne; Patin, Etienne; Condroyer, Christel; Leutenegger, Anne-Louise; ... Brice, Alexis 2010
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 Mutations in the glucocerebrosidase gene confer a risk for Parkinson disease in North Africa Lesage, S; Condroyer, C; Hecham, N; Anheim, M; ... Brice, A 2011
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 Perturbations in ataxia telangiectasia mutant signaling pathways after drug-induced acute liver failure and their reversal during rescue of animals by cell therapy Bandi, Sriram; Joseph, Brigid; Berishvili Berney, Ekaterine; Singhania, Rohit; ... Gupta, Sanjeev 2011
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 Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study Ross, Owen A 2011
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 Imaging findings in a child with Loeys-Dietz syndrome Dhouib, Amira; Beghetti, Maurice; Didier, Dominique 2012
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 Precision medicine for monogenic diabetes: from a survey to the development of a next-generation diagnostic panel Kherra, Sakina; Blouin, Jean-Louis; Santoni, Federico; Schwitzgebel Luscher, Valérie 2017