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Cystinuria subtype and the risk of nephrolithiasis.
Goodyer P, Saadi I, Ong P, Elkas G, Rozen R. Goodyer P, et al. Among authors: saadi i. Kidney Int. 1998 Jul;54(1):56-61. doi: 10.1046/j.1523-1755.1998.00957.x. Kidney Int. 1998. PMID: 9648063 Free article.
THPO-MPL pathway and bone marrow failure.
Dasouki M, Saadi I, Ahmed SO. Dasouki M, et al. Among authors: saadi i. Hematol Oncol Stem Cell Ther. 2015 Mar;8(1):6-9. doi: 10.1016/j.hemonc.2014.11.005. Epub 2014 Nov 29. Hematol Oncol Stem Cell Ther. 2015. PMID: 25482588 Free article.
Mutations in SPECC1L, encoding sperm antigen with calponin homology and coiled-coil domains 1-like, are found in some cases of autosomal dominant Opitz G/BBB syndrome.
Kruszka P, Li D, Harr MH, Wilson NR, Swarr D, McCormick EM, Chiavacci RM, Li M, Martinez AF, Hart RA, McDonald-McGinn DM, Deardorff MA, Falk MJ, Allanson JE, Hudson C, Johnson JP, Saadi I, Hakonarson H, Muenke M, Zackai EH. Kruszka P, et al. Among authors: saadi i. J Med Genet. 2015 Feb;52(2):104-10. doi: 10.1136/jmedgenet-2014-102677. Epub 2014 Nov 20. J Med Genet. 2015. PMID: 25412741 Free PMC article.
SPECC1L regulates palate development downstream of IRF6.
Hall EG, Wenger LW, Wilson NR, Undurty-Akella SS, Standley J, Augustine-Akpan EA, Kousa YA, Acevedo DS, Goering JP, Pitstick L, Natsume N, Paroya SM, Busch TD, Ito M, Mori A, Imura H, Schultz-Rogers LE, Klee EW, Babovic-Vuksanovic D, Kroc SA, Adeyemo WL, Eshete MA, Bjork BC, Suzuki S, Murray JC, Schutte BC, Butali A, Saadi I. Hall EG, et al. Among authors: saadi i. Hum Mol Genet. 2020 Mar 27;29(5):845-858. doi: 10.1093/hmg/ddaa002. Hum Mol Genet. 2020. PMID: 31943082 Free PMC article.
69 results