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	41.	Learning and memory in children with Noonan syndrome. [electronic resource] by Pierpont, Elizabeth I Tworog-Dube, Erica Roberts, Amy E Producer: 20140326 In: American journal of medical genetics. Part A vol. 161A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	42.	A novel SOS1 mutation in Costello/CFC syndrome affects signaling in both RAS and PI3K pathways. [electronic resource] by Tumurkhuu, Munkhtuya Saitoh, Makiko Takita, Junko Mizuno, Yoko Mizuguchi, Masashi Producer: 20130923 In: Journal of receptor and signal transduction research vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	43.	SOS1 mutations are rare in human malignancies: implications for Noonan Syndrome patients. [electronic resource] by Swanson, Kenneth D Winter, Jordan M Reis, Marcelo Bentires-Alj, Mohamed Greulich, Heidi Grewal, Rupinder Hruban, Ralph H Yeo, Charles J Yassin, Yosuf Iartchouk, Oleg Montgomery, Kate Whitman, Susan P Caligiuri, Michael A Loh, Mignon L Gilliland, D Gary Look, A Thomas Kucherlapati, Raju Kern, Scott E Meyerson, Matthew Neel, Benjamin G Producer: 20080505 In: Genes, chromosomes & cancer vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	44.	Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome. [electronic resource] by Tartaglia, Marco Pennacchio, Len A Zhao, Chen Yadav, Kamlesh K Fodale, Valentina Sarkozy, Anna Pandit, Bhaswati Oishi, Kimihiko Martinelli, Simone Schackwitz, Wendy Ustaszewska, Anna Martin, Joel Bristow, James Carta, Claudio Lepri, Francesca Neri, Cinzia Vasta, Isabella Gibson, Kate Curry, Cynthia J Siguero, Juan Pedro López Digilio, Maria Cristina Zampino, Giuseppe Dallapiccola, Bruno Bar-Sagi, Dafna Gelb, Bruce D Producer: 20070221 In: Nature genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	45.	High-Affinity Interactions of the nSH3/cSH3 Domains of Grb2 with the C-Terminal Proline-Rich Domain of SOS1. [electronic resource] by Liao, Tsung-Jen Jang, Hyunbum Nussinov, Ruth Fushman, David Producer: 20201109 In: Journal of the American Chemical Society vol. 142 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	46.	Noonan-like/multiple giant cell lesion syndrome in two adult patients with SOS1 gene mutations. [electronic resource] by Slezak, Ryszard Luczak, Klaudiusz Kalscheuer, Vera Neumann, Thomas E Sasiadek, Maria M Producer: 20100901 In: Clinical dysmorphology vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	47.	Discovery of Aminopiperidine Indoles That Activate the Guanine Nucleotide Exchange Factor SOS1 and Modulate RAS Signaling. [electronic resource] by Abbott, Jason R Hodges, Timothy R Daniels, R Nathan Patel, Pratiq A Kennedy, J Phillip Howes, Jennifer E Akan, Denis T Burns, Michael C Sai, Jiqing Sobolik, Tammy Beesetty, Yugandhar Lee, Taekyu Rossanese, Olivia W Phan, Jason Waterson, Alex G Fesik, Stephen W Producer: 20190624 In: Journal of medicinal chemistry vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	48.	Ulerythema ophryogenes, a rarely reported cutaneous manifestation of noonan syndrome: case report and review of the literature. [electronic resource] by Li, Kayi Ann Thomas, Mary Haber, Richard M Producer: 20130730 In: Journal of cutaneous medicine and surgery vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	49.	Mutation analysis of Son of Sevenless in juvenile myelomonocytic leukemia. [electronic resource] by Kratz, C P Niemeyer, C M Thomas, C Bauhuber, S Matejas, V Bergsträsser, E Flotho, C Flores, N J Haas, O Hasle, H van den Heuvel-Eibrink, M M Kucherlapati, R S Lang, P Roberts, A E Starý, J Strahm, B Swanson, K D Trebo, M Zecca, M Neel, B Locatelli, F Loh, M L Zenker, M Producer: 20070604 In: Leukemia vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	50.	Decreased expression of FGFR1, SOS1, RAF1 genes in cryptorchidism. [electronic resource] by Hadziselimovic, N O de Geyter, Ch Demougin, P Oakeley, E J Hadziselimovic, Faruk Producer: 20100729 In: Urologia internationalis vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	51.	Mutation-Specific Mechanisms of Hyperactivation of Noonan Syndrome SOS Molecules Detected with Single-molecule Imaging in Living Cells. [electronic resource] by Nakamura, Yuki Umeki, Nobuhisa Abe, Mitsuhiro Sako, Yasushi Producer: 20190716 In: Scientific reports vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	52.	A simple improvement in expression cloning. [electronic resource] by Takemoto, Y Furuta, M Sato, M Hashimoto, Y Producer: 19970725 In: DNA and cell biology vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	53.	Multiple spinal nerve enlargement and SOS1 mutation: Further evidence of overlap between neurofibromatosis type 1 and Noonan phenotype. [electronic resource] by Santoro, C Giugliano, T Melone, M A B Cirillo, M Schettino, C Bernardo, P Cirillo, G Perrotta, S Piluso, G Producer: 20180806 In: Clinical genetics vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	54.	A novel locus for autosomal dominant hereditary gingival fibromatosis, GINGF3, maps to chromosome 2p22.3-p23.3. [electronic resource] by Ye, X Shi, L Cheng, Y Peng, Q Huang, S Liu, J Huang, M Peng, B Bian, Z Producer: 20051021 In: Clinical genetics vol. 68 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	55.	Notch and Ras promote sequential steps of excretory tube development in C. elegans. [electronic resource] by Abdus-Saboor, Ishmail Mancuso, Vincent P Murray, John I Palozola, Katherine Norris, Carolyn Hall, David H Howell, Kelly Huang, Kai Sundaram, Meera V Producer: 20111014 In: Development (Cambridge, England) vol. 138 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	56.	Light Chain 3 associates with a Sos1 guanine nucleotide exchange factor: its significance in the Sos1-mediated Rac1 signaling leading to membrane ruffling. [electronic resource] by Furuta, Shuichi Miura, Koichi Copeland, Terry Shang, Wei Hao Oshima, Aki Kamata, Tohru Producer: 20021024 In: Oncogene vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	57.	Mechanism of SOS PR-domain autoinhibition revealed by single-molecule assays on native protein from lysate. [electronic resource] by Lee, Young Kwang Low-Nam, Shalini T Chung, Jean K Hansen, Scott D Lam, Hiu Yue Monatrice Alvarez, Steven Groves, Jay T Producer: 20181126 In: Nature communications vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	58.	Childhood Rhabdomyosarcoma in Association With a RASopathy Clinical Phenotype and Mosaic Germline SOS1 Duplication. [electronic resource] by Salem, Baheyeldin Hofherr, Sean Turner, Joyce Doros, Leslie Smpokou, Patroula Producer: 20170829 In: Journal of pediatric hematology/oncology vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	59.	Hereditary gingival fibromatosis: characteristics and novel putative pathogenic mechanisms. [electronic resource] by Häkkinen, L Csiszar, A Producer: 20070223 In: Journal of dental research vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	60.	FOXI2: a possible gene contributing to ectodermal dysplasia. [electronic resource] by Kurban, Mazen Zeineddine, Savo Bou Hamie, Lamiaa Safi, Remi Abbas, Ossama Kibbi, Abdul Ghani Bitar, Fadi Nemer, Georges Producer: 20180816 In: European journal of dermatology : EJD vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 311 results.