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Articles cités 67

Date

Titre

Auteur·ices

2020-12-23

Molecular dynamics with coupling to an external bath

Daniel Jacobson
2013-07-11

Gain-of-function mutations in RIT1 cause Noonan syndrome, a RAS/MAPK pathway syndrome
2013

The RASopathies
2013-01-26

Noonan syndrome

Marco Tartaglia, Bruce D. Gelb, Judith Allanson
2013-07-07

Exome sequencing identifies secondary mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemia.

Kenichi Yoshida, Yusuke Okuno
2013-03-18

Autoimmunity and persistent RAS-mutated clones long after the spontaneous regression of JMML

Masataka Sugimoto
2012-10-11

Diverging gain-of-function mechanisms of two novel KRAS mutations associated with Noonan and cardio-facio-cutaneous syndromes

Lothar Gremer, Martin Zenker
2012-07-02

Genes2FANs: connecting genes through functional association networks

Avi Ma'ayan
2012-01-01

Biochemical assays to characterize Rho GTPases
2011-06

The Ras-ERK and PI3K-mTOR pathways: cross-talk and compensation
2011-10-13

RAS oncogenes: weaving a tumorigenic web

Dafna Bar-Sagi, Elda Grabocka
2011-03-01

Recent advances in the pathogenesis and treatment of juvenile myelomonocytic leukaemia
2011-04-15

Cancer in Noonan, Costello, cardiofaciocutaneous and LEOPARD syndromes

Suthee Rapisuwon, Henrik Hasle, Philip S. Rosenberg
2011-02-01

Noonan syndrome and clinically related disorders

Marco Tartaglia, Bruce D. Gelb, Martin Zenker
2011-09-08

Gene mutations in the Ras pathway and the prognostic implication in Korean patients with juvenile myelomonocytic leukemia.

Chang-Seok Ki
2010-05

The molecular pathology of cancer
2010-12-01

Activation of multiple signaling pathways causes developmental defects in mice with a Noonan syndrome–associated Sos1 mutation
2010-10-19

Disorders of dysregulated signal traffic through the RAS-MAPK pathway: phenotypic spectrum and molecular mechanisms

Marco Tartaglia, Bruce D. Gelb
2010-12-09

Germline KRAS mutations cause aberrant biochemical and physical properties leading to developmental disorders

Lothar Gremer, Alfred Wittinghofer, Martin Zenker
2010-10-19

Genetic typing of CBL, ASXL1, RUNX1, TET2 and JAK2 in juvenile myelomonocytic leukaemia reveals a genetic profile distinct from chronic myelomonocytic leukaemia.

Michaela Fontenay, Claude Preudhomme, Aline Renneville, André Baruchel, Olivier Kosmider, Bruno Cassinat, Sophie Kaltenbach, Yves Bertrand, Christine Chomienne
2009-09

Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair

Bruno Dallapiccola, Giuseppe Zampino, Wendy Schackwitz, Anna Sarkozy, Viviana Cordeddu, Kerstin Kutsche, Marco Tartaglia, Francesca Lepri, Elisabetta Flex, Laura Mazzanti, Elia Di Schiavi, Avi Ma'ayan, Bruce D. Gelb, Martin Zenker, Anna Lipzen, Len A. Pennacchio
2009-07-22

Detection of two novel mutations and relatively high incidence of H-RAS mutations in Vietnamese oral cancer
2009-06-01

In vitro GEF and GAP assays.
2009-04-01

EGFR and K-ras mutations along the spectrum of pulmonary epithelial tumors of the lung and elaboration of a combined clinicopathologic and molecular scoring system to predict clinical responsiveness to EGFR inhibitors.

Alessandro Sgambato, Antonio Rossi
2008-05-27

Leopard syndrome

Bruno Dallapiccola, Anna Sarkozy
2008-11-13

Noonan syndrome/leukemia-associated gain-of-function mutations in SHP-2 phosphatase (PTPN11) enhance cell migration and angiogenesis
2008-06-12

Juvenile myelomonocytic leukemia and chronic myelomonocytic leukemia

Peter D. Emanuel
2008-06-01

Mapping the nucleotide and isoform-dependent structural and dynamical features of Ras proteins

J. Andrew McCammon
2008-03-27

Diverse driving forces underlie the invariant occurrence of the T42A, E139D, I282V and T468M SHP2 amino acid substitutions causing Noonan and LEOPARD syndromes

Marco Tartaglia, Paola Torreri, Alessandro Grottesi, Gianfranco Bocchinfuso, Lorenzo Stella, Luisa Castagnoli, Bruce D. Gelb, Gianni Cesareni
2008-03-01

Paediatric myelodysplastic syndromes and juvenile myelomonocytic leukaemia: molecular classification and treatment options
2008-01-01

Genotype-phenotype correlation in cases of juvenile myelomonocytic leukemia with clonal RAS mutations

Henrik Hasle, Marco Zecca
2007-12-01

Shp2 knockdown and Noonan/LEOPARD mutant Shp2-induced gastrulation defects

Daphne van Geemen

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