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162 Possible Causes for 25 30, 90S, S, of, preribosome, subcomplex

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  • Familial Infantile Bilateral Striatal Necrosis

    Bernad R, Engelsma D, Sanderson H, Pickersgill H, Fornerod M (2006) Nup214-Nup88 nucleoporin subcomplex is required for CRM1-mediated 60 S preribosomal nuclear export.[journals.plos.org] Review with no image -- 10/ 7/ 6/ 10 CAD/ 70 Yuan/ 1110 Yen Review with an image -- 25/ 18/ 15/ 25 CAD/ 150 Yuan/ 2500 Yen 1st to review with an image -- 50/ 35/ 30/ 50 CAD[novusbio.com] Journal Brain Dev 27:527-30 (2005) DOI: 10.1016/j.braindev.2004.12.004 Reference PMID: 7668837 Authors Thyagarajan D, Shanske S, Vazquez-Memije M, De Vivo D, DiMauro S Title[genome.jp] Nup62·58·54 subcomplex is a nucleoporin subcomplex in the NPC’s central channel, the molecular structure of which, is not known so far.[ediss.uni-goettingen.de] PRO_0000082128 1 – 226 ATP synthase subunit a Add BLAST 226 Proteomic databases PTM databases Expression i Gene expression databases Bgee i ENSG00000198899 Expressed in 90[uniprot.org] . , Motameny , S. , et al . ( 2013 ). Homozygous missense mutation of NDUFV1 as the cause of infantile bilateral striatal necrosis . Neurogenetics . 14 ( 1 ): 85–7 .[cambridge.org]

    Missing: of
  • Isolated Complex I Deficiency

    Recurrence risk was estimated as 20 to 25%.[neurology.org] ., Zhang, S.[monash.edu] Mitochondria are specialized compartments in cells that create more than 90% of the energy needed by the body.[rarediseases.info.nih.gov] Native PAGE with subsequent immunoblotting for complex V revealed impaired complex V assembly and accumulation of ATPase subcomplexes.[infona.pl] ., 2012, Vol. 212(2) : 90-91.[klinikum.uni-muenster.de] Respiration on Arabidopsis leaves was measured in the dark at 25 C. Plants were dark adapted for at least 30 min prior to the excision of leaf discs (7 mm in diameter).[plantphysiol.org]

    Missing: of preribosome
  • Epithelioid Cell Sarcoma

    In comparison, in the Rhabdoid cell lines harboring anti-BRM shRNA, we only observed 25-30% growth inhibition after BAF47 re-expression (Figure 6D).[doi.org] Ott and Sam S.[doi.org] In conclusion, similar to MRT of infancy, loss of INI1 expression is characteristic of both conventional and proximal-type ES, being detected in 90% of cases.[ncbi.nlm.nih.gov] Fornerod M , van Deursen J , van Baal S , Reynolds A , Davis D , Murti KG , Fransen J and Grosveld G ( 1997b ) The human homologue of yeast CRM1 is in a dynamic subcomplex[doi.org] Keratin 95% Low molecular weight keratin CK8 is positive in 95% High molecular weight keratins rare to 50% CK7 22% and CK20 0-15% INI1 loss in 91% EMA 95% Vimentin 95% CA125 90%[surgpathcriteria.stanford.edu] , 30 The term ‘MERT’ should be applied only to primitive malignant neoplasms showing at least in part rhabdoid morphology, almost always showing SMARCB1 protein loss and[nature.com]

    Missing: of preribosome
  • Azorhizobium Caulinodans

    Sum totals of evolved H 2 (2e – reduction) at 72 hr are 230 30 µmol per 10 9 cells, representing net oxidation of some 25% of total (340 µmol) succinate supplied these cultures[journals.plos.org] […] and S. punctata [ 7 ].[biomedcentral.com] .: #20218] INSDC Sequence TPA: Azorhizobium caulinodans ORS 571 tRNA-Ser-CGA-1-1 gene LK001342 90 438753 * [Ref.: #20218] INSDC Sequence TPA: Azorhizobium caulinodans ORS[bacdive.dsmz.de] .: (1) 45 68 88 17; Fax: (1) 45 68 87 90.[academic.oup.com] As a result, the editorial board of Bergey s Manual Trust, in collaboration with more than 500 of the world s leading authorities in prokaryotic systematics, is in the process[books.google.es] In pairwise primary amino acid sequence alignments, four Hyq proteins (HyqBCEF) and four L O subcomplex NuoHJLM proteins are 60% conserved ( Table 1 ; Figs.[journals.plos.org]

    Missing: of preribosome
  • Diabetes Mellitus

    […] from 5 to 30 years.[doi.org] E , Roby K , Sayer J , Shah S , Smith S , Sutherland S , Thorne H , Timadjer A , Vandenberg K , Willett M , Wincott M , Wise C , Woods J , Yates S , Alexander A , Beebe S[ncbi.nlm.nih.gov] A sensitivity analysis of trials comparing DBP targets 80 mmHg (as suggested in clinical guidelines) versus 90 mmHg showed similar results.[ncbi.nlm.nih.gov] […] localizer of BRCA2 ), which is involved in stability of key nuclear structures including chromatin and the nuclear matrix; NDUFAB1 (NADH dehydrogenase (ubiquinone) 1, alpha/beta subcomplex[doi.org] RESULTS: The search yielded 25 prospective cohort studies (N 1.2 million participants) that reported 45 844 incident cases of diabetes during a study follow-up period ranging[ncbi.nlm.nih.gov] […] year earlier, obesity with body mass index 32.2 kg/m2, waist circumference of 113 cm, diffuse goiter with neck circumference 40 cm, and hypertension with blood pressure 140/90[ncbi.nlm.nih.gov]

    Missing: of preribosome
  • Schizophrenia

    Parasitol Res . 1998 ; 84 : 2530 . DOI PubMed Halonen SK , Lyman WD , Chiu FC . Growth and development of Toxoplasma gondii in human neurons and astrocytes.[wwwnc.cdc.gov] Favrod , J , Rexhaj , S , Bardy , S , Ferrari , P , Hayoz , C , Moritz , S , Conus , P , Bonsack , C ( 2014 ).[doi.org] Studies included in the meta-analysis observed a cohort of schizophrenic patients for at least 2 years, with at least 90% follow-up, and reported suicides.[ncbi.nlm.nih.gov] J Bioenerg Biomembr 31:129–135 PubMed CrossRef Google Scholar Zickermann V, Zwicker K, Tocilescu MA, Kerscher S, Brandt U (2007) Characterization of a subcomplex of mitochondrial[dx.doi.org] Of the 90 participants 59 were male and 31 were female. The participants were broadly similar in the two studies.[doi.org] […] outcomes in three studies.[30] [35] [38] Eight studies were at high risk of bias because participants or staff were not blind,[23] [25] [28][29][30] [35] [37] [38] which was[doi.org]

    Missing: of preribosome
  • Anaplastic Large Cell Lymphoma

    Gene Name NPM1 (nucleophosmin) Location 5q35.1 Protein Nuclear localisation; RNA binding nucleolar phosphoprotein involved in preribosomal assembly.[atlasgeneticsoncology.org] ; however, a relatively high relapse rate was observed (25-30% ).[ncbi.nlm.nih.gov] […] expression in S-ALCL.[jhoonline.biomedcentral.com] The response rate is high at 80-90%; however, once the disease progresses in patients on BV, survival outcome is very poor, with a median overall survival of less than two[ncbi.nlm.nih.gov] Results The overall response rates for patients with ALCL treated at doses of 165 (ALCL165) and 280 (ALCL280) mg/m 2 were 83% and 90%, respectively.[ncbi.nlm.nih.gov] CD30 LPDs comprise approximately 25%-30% of primary cutaneous lymphomas and as a group represent the second most common clonal T-cell neoplasm of the skin behind mycosis fungoides[ncbi.nlm.nih.gov]

    Missing: of subcomplex
  • Werner Syndrome

    Nucleic Acids Res. 19 , 969 (1991). 30 Aram, H. & Fatourechi, V. Cutis 14 , 215–218 (1974). 31 Cerimele, D. et al. Hum. Genet. 62 , 2530 (1982). 32 Samantray, S.[dx.doi.org] Defective production of WRN protein was confirmed by Western blotting, although the three representative mutations in Japanese patients, mutations 1, 4 and 6, which include over 90%[ncbi.nlm.nih.gov] Our results indicate that WRN interacts directly or is very closely associated in either a single multiprotein complex or in independent subcomplexes with RAD51, RAD54 and[doi.org] [New York: Penguin, 1984], 25). 30. Ibid., 47-48. 31. Burke K.[books.google.ro] RESULTS: The existing diagnostic criteria were reviewed, and signs with 90% incidence were listed as cardinal signs.[ncbi.nlm.nih.gov] […] only eight (8.4%) of 95 non-Werner's syndrome FL cell cultures demonstrated VTM: seven with low-grade VTM (approximately 5% of 300 metaphases), and one with VTM affecting 90[ncbi.nlm.nih.gov]

    Missing: of preribosome
  • Gorlin Syndrome

    -30.[sjeldnediagnoser.no] G, van Sluis P, Volckmann R, Koster J, Versteeg R, Schmidt S, Wolf S, Lawerenz C, Bartholomae CC, von Kalle C, Unterberg A, Herold-Mende C, Hofer S, Kulozik AE, von Deimling[ncbi.nlm.nih.gov] […] testing, by Sanger sequencing and multiplex ligation-dependent probe amplification (MLPA) to confirm a clinical diagnosis of Gorlin syndrome, identifies a mutation in 60-90[ncbi.nlm.nih.gov] The asterisk marks degradation products of MBP–Orc1. ( C ) Subunit interactions within the human Orc2-Orc3–Orc6 subcomplex.[elifesciences.org] In 90% of the patients, nevoid basal cell carcinoma syndrome is associated with recurring odontogenic keratocysts.[moh-it.pure.elsevier.com] 27 , 29 , 30 , 34 – 39 ].[pubmedcentral.nih.gov]

    Missing: of preribosome
  • Fanconi Anemia

    -30%, which continues to rise with the patient's age. [ 2 ] Liver adenoma/hepatomas predominantly affect those who have had anaemia treated by androgens.[patient.info] Colocalization of activated FANCD2 and BRCA1 in discrete nuclear foci during S phase. (A) HeLa cells were synchronized at G 1 /S with mimosine and released into S phase.[doi.org] Actuarial risk of death from hematologic causes was 81% (67% to 90%) by 40 years of age.[ncbi.nlm.nih.gov] FANCA and FANCG consistently copurified with FAAP20 ( Fig. 1 A ), suggesting that these three components likely form a stable subcomplex.[pnas.org] Abstract More than 90% of Fanconi anemia (FA) patients experience progressive bone marrow failure during life with a median onset at 8 years of age.[ncbi.nlm.nih.gov] […] to 30% of affected individuals have developed solid tumors, with the incidence increasing as patients become older.[news-medical.net]

    Missing: of preribosome