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25篇 您的检索式：作者名="Hamdan FF"

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	题名	作者	年代	出处	被引量
1	Cloning of the chaperonin t-complex polypeptide 1 gene from Schistosoma mansoni and studies of its expression levels under heat shock and oxidative stress 显示文摘	Campos EG Hamdan FF	2000	Parasitol Res2000，86，：	1
2	Cloning and characterization of a novel form of tyrosine hydroxylase from the human parasite, Schistosoma mansoni显示文摘	Hamdan FF Ribeiro P	1998	J Neurochem1998，71，4：	1
3	Characterization of a stable form of tryptophan hydroxylase from the human parasite Schistosoma mansoni显示文摘	Hamdan FF Ribeiro P	1999	J Biol Chem1999，274，21：	1
4	Systematic resequeneing of X-ehromosome synaptie genes in autism spectrum disorder and schizophrenia显示文摘	Piton A Gauthier J Hamdan FF	2011	Mol Psychiatry2011，16，8：	1
5	Mutations inC50RFg2 Cause Joubert Syndrome in the French Canadian Population显示文摘	Srour M Schwartzentruber J Hamdan FF	2012	Am J Hum Genet2012，90，4：	1
6	Intellectual disability without epilepsy associated with STXBP1 disruption显示文摘	Hamdan FF Gauthier J Dobrzeniecka S	2011	Eur J Hum Genet2011，19，5：	1
7	Mutations in TMEM231 cause Joubert syndrome in French Canadians 显示文摘	Srour M Hamdan FF Schwartzentruber JA	2012	J Med Genet2012，49，10：	1
8	De novo STXBP1 muta- tions in mental retardation and nonsyndromic epilepsy 显示文摘	Hamdan FF Piton A Gauthier J	2009	Ann Neurol2009，65，6：	1
9	De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment 显示文摘	Hamdan FF Daoud H Rochefort D	2010	Am J Hum Genet2010，87，5：	1
10	A novel Schistosoma mansoni G protein-coupled receptor is responsive to histamine 显示文摘	Hamdan FF Abramovitz M Mousa A	2002	Mol Biochem Parasitol2002，119，：	1
11	De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy 显示文摘	Hamdan FF Piton A Gauthier J	2009	Ann Neurol2009，65，6：	1
12	De novo muta tions in FOXP1 in cases with intellectual disability,autism, and language impairment显示文摘	Hamdan FF Daoud H Rochefort D	2010	Am J Hum Genet2010，87，5：	1
13	Codon optimization improves hetemlogous expression of a Sehistosoma mansoni cDNA in HEK293 cells 显示文摘	Hamdan FF Mousa A Ribeim P	2002	Parasitol Res2002，88，6：	1
14	Laparoscopic versus open distal pancreatectomy: a clinical and cost-effective- ness study显示文摘	Abu HM Hamdan M Di FF	2012	Surg Endosc2012，26，6：	1
15	Mutations in SYNGAPI in autosomal nonsyndromic mental retardation显示文摘	Hamdan FF Gauthier J Spiegelman D	2009	N Eng J Med2009，306，6：	1
16	Conformational changes that occur during M3 muscarinic acetylcholine receptor activation probed by the use of an in situ disulfide cross-linking strategy显示文摘	Hamdan FF Bloodworth LM	2002	J Biol Chem2002，277，：	1
17	Codon optimization improves heterologous expression of a Schistosoma mansoni cDNA in HEK293 cells显示文摘	Hamdan FF Mousa A Ribeiro P	2002	Parasitol Res2002，88，6：	1
18	Mutations in SYN- GAP1 cause intellectual disability, autism, and a specific form of epilepsy by inducing haploinsufficiency 显示文摘	Berryer MH Hamdan FF Klitten LL	2013	Hum Mutat2013，34，2：	1
19	Codon optimization improves heterologous expression of a Schiztosoma mansoni cDNA in HEK293 cells显示文摘	Hamdan FF Mousa A Ribeiro P	2002	Parasitol2002，88，6：	1
20	De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy显示文摘	Hamdan FF Piton A Gauthier J	2009	Ann Neurol2009，65，6：	1

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