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Items: 40

1.

Prevalence of arterial hypertension in the Krasnoyarsk Krai (Siberia, Russia).

Artyukhov IP, Grinshtein YI, Petrova MM, Shabalin VV, Ruf RR.

BMC Cardiovasc Disord. 2017 May 26;17(1):138. doi: 10.1186/s12872-017-0559-5.

2.

Phosphorylation of collapsin response mediator protein-2 disrupts neuronal maturation in a model of adult neurogenesis: Implications for neurodegenerative disorders.

Crews L, Ruf R, Patrick C, Dumaop W, Trejo-Morales M, Achim CL, Rockenstein E, Masliah E.

Mol Neurodegener. 2011 Sep 24;6:67. doi: 10.1186/1750-1326-6-67.

3.

Comparative genome sequencing of an isogenic pair of USA800 clinical methicillin-resistant Staphylococcus aureus isolates obtained before and after daptomycin treatment failure.

Boyle-Vavra S, Jones M, Gourley BL, Holmes M, Ruf R, Balsam AR, Boulware DR, Kline S, Jawahir S, Devries A, Peterson SN, Daum RS.

Antimicrob Agents Chemother. 2011 May;55(5):2018-25. doi: 10.1128/AAC.01593-10. Epub 2011 Feb 22.

4.

Protein (19)F NMR in Escherichia coli.

Li C, Wang GF, Wang Y, Creager-Allen R, Lutz EA, Scronce H, Slade KM, Ruf RA, Mehl RA, Pielak GJ.

J Am Chem Soc. 2010 Jan 13;132(1):321-7. doi: 10.1021/ja907966n.

5.

19F NMR studies of alpha-synuclein conformation and fibrillation.

Li C, Lutz EA, Slade KM, Ruf RA, Wang GF, Pielak GJ.

Biochemistry. 2009 Sep 15;48(36):8578-84. doi: 10.1021/bi900872p.

6.

Alpha-Synuclein conformation affects its tyrosine-dependent oxidative aggregation.

Ruf RA, Lutz EA, Zigoneanu IG, Pielak GJ.

Biochemistry. 2008 Dec 23;47(51):13604-9. doi: 10.1021/bi801884z.

7.

The CAIRP (CAndesartan for In-stent Restenosis Prevention) Trial--a multicenter study of AT1-receptor blocker therapy in coronary stenting.

Krämer J, Ruf RG, Schmidt S, Axthelm C, Strasser R, Janssen G, Thieme T, Kusch A, Waigand J, Dietz R, Gross CM.

J Invasive Cardiol. 2008 May;20(5):205-10.

8.

Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9.

Mucha B, Ozaltin F, Hinkes BG, Hasselbacher K, Ruf RG, Schultheiss M, Hangan D, Hoskins BE, Everding AS, Bogdanovic R, Seeman T, Hoppe B, Hildebrandt F; Members of the APN Study Group.

Pediatr Res. 2006 Feb;59(2):325-31.

PMID:
16439601
9.

Lactate in a laubenpieper.

Derer W, Elitok S, Claus T, Schütt H, Ruf R, Kettritz R, Luft FC, Pilz B.

Nephrol Dial Transplant. 2005 Dec;20(12):2851-4. Epub 2005 Oct 12.

PMID:
16221720
10.

Mapping a new suggestive gene locus for autosomal dominant nephrolithiasis to chromosome 9q33.2-q34.2 by total genome search for linkage.

Wolf MT, Zalewski I, Martin FC, Ruf R, Müller D, Hennies HC, Schwarz S, Panther F, Attanasio M, Acosta HG, Imm A, Lucke B, Utsch B, Otto E, Nurnberg P, Nieto VG, Hildebrandt F.

Nephrol Dial Transplant. 2005 May;20(5):909-14. Epub 2005 Mar 1.

PMID:
15741201
11.

No evidence for genotype/phenotype correlation in NPHS1 and NPHS2 mutations.

Schultheiss M, Ruf RG, Mucha BE, Wiggins R, Fuchshuber A, Lichtenberger A, Hildebrandt F.

Pediatr Nephrol. 2004 Dec;19(12):1340-8.

12.

Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome.

Ruf RG, Schultheiss M, Lichtenberger A, Karle SM, Zalewski I, Mucha B, Everding AS, Neuhaus T, Patzer L, Plank C, Haas JP, Ozaltin F, Imm A, Fuchshuber A, Bakkaloglu A, Hildebrandt F; APN Study Group.

Kidney Int. 2004 Aug;66(2):564-70.

13.

SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes.

Ruf RG, Xu PX, Silvius D, Otto EA, Beekmann F, Muerb UT, Kumar S, Neuhaus TJ, Kemper MJ, Raymond RM Jr, Brophy PD, Berkman J, Gattas M, Hyland V, Ruf EM, Schwartz C, Chang EH, Smith RJ, Stratakis CA, Weil D, Petit C, Hildebrandt F.

Proc Natl Acad Sci U S A. 2004 May 25;101(21):8090-5. Epub 2004 May 12.

14.

NPHS2 mutation associated with recurrence of proteinuria after transplantation.

Billing H, Müller D, Ruf R, Lichtenberger A, Hildebrandt F, August C, Querfeld U, Haffner D.

Pediatr Nephrol. 2004 May;19(5):561-4. Epub 2004 Mar 10.

15.

Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome.

Ruf RG, Lichtenberger A, Karle SM, Haas JP, Anacleto FE, Schultheiss M, Zalewski I, Imm A, Ruf EM, Mucha B, Bagga A, Neuhaus T, Fuchshuber A, Bakkaloglu A, Hildebrandt F; Arbeitsgemeinschaft Für Pädiatrische Nephrologie Study Group.

J Am Soc Nephrol. 2004 Mar;15(3):722-32.

16.

Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination.

Otto EA, Schermer B, Obara T, O'Toole JF, Hiller KS, Mueller AM, Ruf RG, Hoefele J, Beekmann F, Landau D, Foreman JW, Goodship JA, Strachan T, Kispert A, Wolf MT, Gagnadoux MF, Nivet H, Antignac C, Walz G, Drummond IA, Benzing T, Hildebrandt F.

Nat Genet. 2003 Aug;34(4):413-20.

17.

A gene locus for branchio-otic syndrome maps to chromosome 14q21.3-q24.3.

Ruf RG, Berkman J, Wolf MT, Nurnberg P, Gattas M, Ruf EM, Hyland V, Kromberg J, Glass I, Macmillan J, Otto E, Nurnberg G, Lucke B, Hennies HC, Hildebrandt F.

J Med Genet. 2003 Jul;40(7):515-9. No abstract available.

18.

Identification of the first gene locus (SSNS1) for steroid-sensitive nephrotic syndrome on chromosome 2p.

Ruf RG, Fuchshuber A, Karle SM, Lemainque A, Huck K, Wienker T, Otto E, Hildebrandt F.

J Am Soc Nephrol. 2003 Jul;14(7):1897-900.

19.

A gene locus for steroid-resistant nephrotic syndrome with deafness maps to chromosome 14q24.2.

Ruf RG, Wolf MT, Hennies HC, Lucke B, Zinn C, Varnholt V, Lichtenberger A, Pasch A, Imm A, Briese S, Lennert T, Fuchshuber A, Nurnberg P, Hildebrandt F.

J Am Soc Nephrol. 2003 Jun;14(6):1519-22.

20.

Heme oxygenase-1 attenuates ischemia/reperfusion-induced apoptosis and improves survival in rat renal allografts.

Wagner M, Cadetg P, Ruf R, Mazzucchelli L, Ferrari P, Redaelli CA.

Kidney Int. 2003 Apr;63(4):1564-73.

21.

Confirmation of the ATP6B1 gene as responsible for distal renal tubular acidosis.

Ruf R, Rensing C, Topaloglu R, Guay-Woodford L, Klein C, Vollmer M, Otto E, Beekmann F, Haller M, Wiedensohler A, Leumann E, Antignac C, Rizzoni G, Filler G, Brandis M, Weber JL, Hildebrandt F.

Pediatr Nephrol. 2003 Feb;18(2):105-9. Epub 2002 Dec 18.

PMID:
12579397
22.

A gene mutated in nephronophthisis and retinitis pigmentosa encodes a novel protein, nephroretinin, conserved in evolution.

Otto E, Hoefele J, Ruf R, Mueller AM, Hiller KS, Wolf MT, Schuermann MJ, Becker A, Birkenhäger R, Sudbrak R, Hennies HC, Nürnberg P, Hildebrandt F.

Am J Hum Genet. 2002 Nov;71(5):1161-7. Epub 2002 Aug 29.

23.

C2-C8 hydrocarbon measurement and quality control procedures at the Global Atmosphere Watch Observatory Hohenpeissenberg.

Plass-Dülmer C, Michl K, Ruf R, Berresheim H.

J Chromatogr A. 2002 Apr 12;953(1-2):175-97.

PMID:
12058932
24.

Molecular cloning of the critical region for glomerulopathy with fibronectin deposits (GFND) and evaluation of candidate genes.

Vollmer M, Kremer M, Ruf R, Miot S, Nothwang HG, Wirth J, Otto E, Krapf R, Hildebrandt F.

Genomics. 2000 Sep 1;68(2):127-35.

PMID:
10964510
25.

Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome.

Konrad M, Vollmer M, Lemmink HH, van den Heuvel LP, Jeck N, Vargas-Poussou R, Lakings A, Ruf R, Deschênes G, Antignac C, Guay-Woodford L, Knoers NV, Seyberth HW, Feldmann D, Hildebrandt F.

J Am Soc Nephrol. 2000 Aug;11(8):1449-59.

26.

A Bartter's syndrome mutation of ROMK1 exerts dominant negative effects on K(+) conductance.

Kunzelmann K, Hübner M, Vollmer M, Ruf R, Hildebrandt F, Greger R, Schreiber R.

Cell Physiol Biochem. 2000;10(3):117-24.

27.

The gene for human fibronectin glomerulopathy maps to 1q32, in the region of the regulation of complement activation gene cluster.

Vollmer M, Jung M, Rüschendorf F, Ruf R, Wienker T, Reis A, Krapf R, Hildebrandt F.

Am J Hum Genet. 1998 Dec;63(6):1724-31.

28.

[Strategy and results of advanced tumors in emergency situations].

Ruf C, Kohlberger E, Ruf RH, Farthmann EH.

Langenbecks Arch Chir Suppl Kongressbd. 1996;113:183-5. German.

PMID:
9101825
29.

Restricted electron motion in a one-dimensional organic conductor: Pulsed-gradient spin-echo ESR in (fluoroanthene)2PF6.

Kaplan N, Dormann E, Ruf R, Coy A, Callaghan PT.

Phys Rev B Condens Matter. 1995 Dec 15;52(23):16385-16394. No abstract available.

PMID:
9981036
30.

Restricted diffusion of the conduction electrons in quasi-one-dimensional organic conductors.

Ruf R, Kaplan N, Dormann E.

Phys Rev Lett. 1995 Mar 13;74(11):2122-2125. No abstract available.

PMID:
10057847
31.

Magneto-optical properties of CrO2.

Brändle H, Weller D, Parkin SS, Scott JC, Fumagalli P, Reim W, Gambino RJ, Ruf R, Güntherodt G.

Phys Rev B Condens Matter. 1992 Dec 1;46(21):13889-13895. No abstract available.

PMID:
10003453
32.

Observation of vacuum tunneling of spin-polarized electrons with the scanning tunneling microscope.

Wiesendanger R, Güntherodt H, Güntherodt G, Gambino RJ, Ruf R.

Phys Rev Lett. 1990 Jul 9;65(2):247-250. No abstract available.

PMID:
10042590
33.

CrO2-a new half-metallic ferromagnet?

Kämper KP, p Schmitt W, Güntherodt G, Gambino RJ, Ruf R.

Phys Rev Lett. 1987 Dec 14;59(24):2788-2791. No abstract available.

PMID:
10035648
34.

[Mandibular bone tumors. Diagnostic difficulties].

Leyder P, Ruf R, Texier J, Laufer J.

Rev Stomatol Chir Maxillofac. 1984;85(4):320-4. French.

PMID:
6593798
35.

[Cervico-facial suppuration of oro-dental origin due to Eikenella corrodens].

Ruf R, Ruf C, Felten A, Ortenberg M, Laufer J.

Rev Stomatol Chir Maxillofac. 1984;85(4):284-6. French.

PMID:
6387877
36.

[Thrombopenia as the presenting symptom of acute disseminated lupus erythematosus: Moschcowitz's disease].

Bourrier P, Cousteau C, Gounant C, Grodner F, Ruf R, Szpirglas H, Texier J, Laufer J.

Rev Stomatol Chir Maxillofac. 1983;84(4):196-8. French.

PMID:
6579593
37.

[Malignant non-Hodgkin's lymphoma].

Bourrier P, Grodner F, Ruf R, Texier J, Cottencin R, Cousteau C, Deslandre A, Gounant C, Szpirglas H, Laufer J.

Rev Stomatol Chir Maxillofac. 1983;84(4):190-5. French.

PMID:
6579592
38.

[Fractures].

Ruf R.

Soins. 1982 Apr;27(7):23. French. No abstract available.

PMID:
6919264
39.

[Anomalies of mineralization of the temporal styloid process (author's transl)].

Laufer J, Ruf R.

Rev Stomatol Chir Maxillofac. 1981;82(5):318-24. Review. French.

PMID:
7027429
40.

Treatment of chronic amoebic dysentery infection with terramycin.

RUF R.

Can Med Assoc J. 1955 Jan 15;72(2):132-3. No abstract available.

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