|
|
|
题名
|
作者
|
年代
|
出处
|
被引量
|
| 1 | Crown profile models based on branch attributes in coastal Douglas-fir显示文摘 | RANDY L R DOUGLAS A M | 1997 | For Ecol and Manage1997，96，： | 1 |
| 2 | Bioaccumu- lation of chlorinated pesticides and PCBs in the tropi- cal freshwater ftsb Hoplias malabaricus: Histopathologi- cal, physiological, and immunological findings 显示文摘 | Miranda A L Roche H Randi M A F | 2008 | En- vironment International2008，34，7： | 1 |
| 3 | Aspirin in pregnant pa- tients with essential thrombocythemia: a retrospective analysis of 129 pregnancies显示文摘 | Passamonti F Rumi E Randi M L | 2010 | J Thromb Haemost2010，8，2： | 1 |
| 4 | N-acyl-L-homoserine lactones: a class of bacterial quorum-sensing signals alter post-embryonic root de- velopment in Arabidopsis thaliana 显示文摘 | Randy O C Mignel M T Jose L B | 2008 | Plant Cell Environ2008，31，： | 1 |
| 5 | Search for all self-avoiding paths for molecular graphs显示文摘 | Randi(c) M Brissey G M Spencer R E Wilkins C L | | 0，，： | 1 |
| 6 | Interfacial polymerization of polyaniline nanofibers grafted to Au surfaces显示文摘 | DUSTYN D S RANDY M V RUSSEL A L | 2004 | Chem Mater2004，16，9： | 1 |
| 7 | Carbon monoxide partial pressure effects on the metabolic process of syngas fermentation 显示文摘 | Kendall M H Randy S L | 2010 | Bio- chem Eng J2010，48，2： | 1 |
| 8 | The occasional venous thromboses seen in patients with severe(homozygous)F Ⅻ deficiency are probably due to associated risk factors:a study of prevalence in 21 patients and review of the literature显示文摘 | Girolami A Randi M L Gavasso S | 2004 | J Thromb Thrombolysis2004，17，2： | 1 |
| 9 | The energy partition of underwater sparks显示文摘 | Randy M Roberts Jeffrey A Cook Robert L Rogers | 1996 | J Acoust Soc Am1996，99，6： | 1 |
| 10 | Activation of a Renin-angiotensin System in Ischemic Cardiac Sympathetic Nerve Endings and its Association with Norepinephrine Release显示文摘 | Roberto L Randi B S Christina J M | 2002 | Internati Immunopharmacol2002，2，： | 1 |
| 11 | Duodenal-jejunal exclusion improves glucose tolerance in the diabetic,GotoKakizaki rat by a GLP-1 receptor-mediated mechanism显示文摘 | Tammy L Kindel Stephanie M Yoder Randy J | 2009 | J Gastrointest Surg2009，13，10： | 1 |
| 12 | Antiplatelet glycoprotein autoantibodies in patients with autoimmune diseases with and without thrombocytopenia 显示文摘 | Cordiano I Salvan F Randi M L | 1996 | J Clinical Immunology1996，16，6： | 1 |
| 13 | Attempt to improve the diagnosis of immune thrombocytopenia by combined use of two different platelet autoantibo-dies assays (PAIgG and MACE)显示文摘 | FABRIS F SCANDELLARI R RANDI M L | 2002 | Haematologica2002，87，： | 1 |
| 14 | Genome sequence of the palaeopolyp|oid soybean 显示文摘 | Jeremy S Steven B C Jessica S Ma J X Therese M William N David L H Qijian S Jay J T Cheng J L Xu D Uffe H Gregory D M Yeisoo Y Tetsuya S Taishi U Madan K B Devinder S Babu V Erika L Myron P David G Shu S Q David G Kerrie B Montona F Brian A Du J C Tian Z Zhu L Navdeep G Trupti J Marc L Anand S Zhang X C Kazuo S Henry T N Rod A Perry C James S Jane G Dan R Gary S Randy C S Scott A J | 2010 | Nature2010，463，： | 1 |
| 15 | Crown profile models based on branch attributes in coastal Douglas-fir显示文摘 | RANDY L R DOUGLAS A M | 1997 | For Ecol Manage1997，96，： | 1 |
| 16 | Intranuclear inclusions in a fragile X mosaic male显示文摘Lack of the fragile X mental retardation protein leads to Fragile X syndrome(FXS)while increased levels of FMR1 mRNA,as those observed in premutation carriers can lead to Fragile X-associated tremor ataxia syndrome(FXTAS).Until recently,FXTAS had been observed only in carriers of an FMR1 premutation(55–200 CGG repeats);however the disorder has now been described in individuals carriers of an intermediate allele(45–54 CGG repeats)as well as in a subject with a full mutation with mosaicism.Here,we report on molecular and clinical data of a male FMR1 mosaic individual with full and premutation alleles.Molecular analysis of FMR1 and FMRP expression in this subject is consistent with a FXS phenotype.We observed reduced expression of FMRP in both peripheral blood and brain leading to the FXS diagnosis.In addition,a dramatic 90%depletion of both FMR1 mRNA and FMRP levels was observed in the blood,as normally observed in FXS cases,and an even greater depletion in the brain.A clinical report of this patient,at age 71,described neurodegenerative signs of parkinsonism that were likely,in retrospect,part of a FXTAS scenario as post-mortem examination shows the presence of intranuclear inclusions,the hallmark pathology of FXTAS.The findings presented in this study indicate co-morbidity for both FXS and FXTAS in this individual carrying both full and premutation FMR1 alleles.In addition,based on symptoms and pathological and molecular evidence,this report suggests the need to redefine the diagnostic criteria of FXTAS. | Dalyir I Pretto Michael R Hunsaker Christopher L Cunningham Claudia M Greco Randi J Hagerman Stephen C Noctor Deborah A Hall Paul J Hagerman Flora Tassone | 2013 | Translational Neurodegeneration2013，2，1： | 0 |
您所在的机构暂未开通此部分的功能，请联系管理员