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	题名	作者	年代	出处	被引量
1	Cerebral folate deficiency and CNS inflammatory markers in Alpers disease 显示文摘	HASSELMANN O BLAU N RAMAEKERS V T	2010	MolGenet Metab2010，99，1：	1
2	A novel mutation withinthe miR 96 gene causes non-syndromic inherited hearing loss in anItalian family by altering pre-miRNA processing 显示文摘	Solda G Hobusto M Primignani P	2012	Hum MolGenet2012，21，3：	1
3	The role of N-acetylglucosaminyltransferase III and V in the post-tran-scriptional modifications of E-cadherin 显示文摘	Pinho SS Reis CA Paredes J	2009	Hum MolGenet2009，18，14：	1
4	Over-expression of NYGGF4 (PID1) inhibits glucose transport in skeletal myotubes by blocking the IRS1/PI3K/AKT insulin pathway 显示文摘	Wu WL Gan WH Tong ML	2011	MolGenet Metab2011，102，3：	1
5	Single base polymorphism in the human tumour necrosis factor alpha (TNF alpha)gene detectable by Ncol restriction of PCR product显示文摘	Wilson AG di Giovine FS Blakemore AI	1992	Hum MolGenet1992，1，5：	1
6	Exosomes and microvesicles: extracellular vesicles for genetic information transfer and gene tberapy显示文摘	Lee Y El Andaloussi S Wood MJ	2012	Hum MolGenet2012，21，1：	1
7	ApoE isoform- specific regulation of regeneration in the peripheral nervous system显示文摘	Comley LH Fuller HR Wishart TM	2011	Hum MolGenet2011，20，12：	1
8	A genomic rearrangement resulting in a tandem duplication is associated with split hand-split foot malformation 3 (SHFM3) at 10q24显示文摘	de Mollerat XJ	2003	Hum MolGenet2003，12，：	1
9	A haplotype of the CYP4F2 gene associated with myocardial infraction in Japanese men 显示文摘	Fu ZY Nakayama T Sato N	2009	MolGenet Metab2009，96，3：	1
10	Characterization of fattyacid oxidation in human muscle mitochondria and myoblasts 显示文摘	Djouadi F Bonnefont JP Munnich A	2003	MolGenet Metab2003，78，：	1
11	Fine mapping of t he association with obesity a t the F TO lo cus in A frican-derived po pulations显示文摘	Hassanein M T Lyon H N Nguyen T T :j:	2010	Hum MolGenet2010，19，14：	1
12	Genetic dissection of myocilin glaucoma 显示文摘	Gong G Kosoko-Lasaki	2004	Hum MolGenet2004，13，1：	1
13	The Rb/E2F pathway and cancer显示文摘	NEVIANS J R	2001	Hum MolGenet2001，10，：	1
14	Comprehensive genetic analysis of the platelet activa- ting {actor acetylhydrolase (PLA2GT) gene and cardi- ovascular disease in case-control and family datasets显示文摘	SUTTON B S CROSSLIN D R SHAH S H	2008	Hum MolGenet2008，17，：	1
15	Trehalose reducesaggregate formation and delays pathology in a transgenic mousemodel of oculopharyngeal muscular dystrophy 显示文摘	Davies JE Sarkar S Rubinsztein DC	2006	Hum MolGenet2006，15，1：	1
16	Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome2p显示文摘	Fontaine B Bruyn RP	1994	Hum MolGenet1994，3，：	1
17	Somatic mosaieism in patients with Angelman syndrome and an imprintingdefect显示文摘	Nazlican H Zesehnigk M Claussen U	2004	Hum MolGenet2004，13，：	1
18	A set of differentially expressed miRNAs, including miR-30a-5p, act as posttranscriptional inhibitors of BDNF in prefrontal cortex显示文摘	MELLIOS N HUANG H S GRIGORENKO A etal	2008	Hum MolGenet2008，17，19：	1
19	Synergy between the genes for butyrylcholinesterase K variant and apolipoprotein E4 in late-onset comtirmed Alzheimer's disease显示文摘	Johnston C Smith AD	1997	Hum Molgenet1997，6，：	1
20	Gene expression in early ischemic renal injury: clues towards pathogenesis, biomarker discovery, and novel therapeutics 显示文摘	DEVARAJAN P MISHRA J SUPAVEKIN S	2003	MolGenet Metah2003，80，4：	1

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