Publications
| 1. | CNOT3 Is a Modifier of PRPF31 Mutations in Retinitis Pigmentosa with Incomplete Penetrance. |
| Venturini G, Rose AM, Shah AZ, Bhattacharya SS, Rivolta C. | |
| PLoS Genet. 2012 Nov;8(11):e1003040. doi: 10.1371/journal.pgen.1003040. Epub 2012 Nov 8. | |
| PMID: 23144630 [PubMed - in process] Free PMC Article | |
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| 2. | FAM161A, associated with retinitis pigmentosa, is a component of the cilia-basal body complex and interacts with proteins involved in ciliopathies. |
| Di Gioia SA, Letteboer SJ, Kostic C, Bandah-Rozenfeld D, Hetterschijt L, Sharon D, Arsenijevic Y, Roepman R, Rivolta C. | |
| Hum Mol Genet. 2012 Dec 1;21(23):5174-84. doi: 10.1093/hmg/dds368. Epub 2012 Sep 1. | |
| PMID: 22940612 [PubMed - in process] Free Article | |
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| 3. | Identification of an RP1 Prevalent Founder Mutation and Related Phenotype in Spanish Patients with Early-Onset Autosomal Recessive Retinitis. |
| Avila-Fernandez A, Corton M, Nishiguchi KM, Muñoz-Sanz N, Benavides-Mori B, Blanco-Kelly F, Riveiro-Alvarez R, Garcia-Sandoval B, Rivolta C, Ayuso C. | |
| Ophthalmology. 2012 Aug 20. [Epub ahead of print] | |
| PMID: 22917891 [PubMed - as supplied by publisher] | |
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| 4. | Genes associated with retinitis pigmentosa and allied diseases are frequently mutated in the general population. |
| Nishiguchi KM, Rivolta C. | |
| PLoS One. 2012;7(7):e41902. Epub 2012 Jul 27. | |
| PMID: 22848652 [PubMed - in process] Free PMC Article | |
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| 5. | Clinicopathologic and molecular analysis of a choroidal pigmented schwannoma in the context of a PTEN hamartoma tumor syndrome. |
| Venturini G, Moulin AP, Deprez M, Uffer S, Bottani A, Zografos L, Rivolta C. | |
| Ophthalmology. 2012 Apr;119(4):857-64. Epub 2012 Jan 26. | |
| PMID: 22281088 [PubMed - indexed for MEDLINE] | |
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| 6. | Genomewide association study using a high-density single nucleotide polymorphism array and case-control design identifies a novel essential hypertension susceptibility locus in the promoter region of endothelial NO synthase. |
| Salvi E, Kutalik Z, Glorioso N, Benaglio P, Frau F, Kuznetsova T, Arima H, Hoggart C, Tichet J, Nikitin YP, Conti C, Seidlerova J, Tikhonoff V, Stolarz-Skrzypek K, Johnson T, Devos N, Zagato L, Guarrera S, Zaninello R, Calabria A, Stancanelli B, Troffa C, Thijs L, Rizzi F, Simonova G, Lupoli S, Argiolas G, Braga D, D'Alessio MC, Ortu MF, Ricceri F, Mercurio M, Descombes P, Marconi M, Chalmers J, Harrap S, Filipovsky J, Bochud M, Iacoviello L, Ellis J, Stanton AV, Laan M, Padmanabhan S, Dominiczak AF, Samani NJ, Melander O, Jeunemaitre X, Manunta P, Shabo A, Vineis P, Cappuccio FP, Caulfield MJ, Matullo G, Rivolta C, Munroe PB, Barlassina C, Staessen JA, Beckmann JS, Cusi D. | |
| Hypertension. 2012 Feb;59(2):248-55. Epub 2011 Dec 19. | |
| PMID: 22184326 [PubMed - indexed for MEDLINE] Free PMC Article | |
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| 7. | Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma. |
| Chambers JC, Zhang W, Sehmi J, Li X, Wass MN, Van der Harst P, Holm H, Sanna S, Kavousi M, Baumeister SE, Coin LJ, Deng G, Gieger C, Heard-Costa NL, Hottenga JJ, Kühnel B, Kumar V, Lagou V, Liang L, Luan J, Vidal PM, Mateo Leach I, O'Reilly PF, Peden JF, Rahmioglu N, Soininen P, Speliotes EK, Yuan X, Thorleifsson G, Alizadeh BZ, Atwood LD, Borecki IB, Brown MJ, Charoen P, Cucca F, Das D, de Geus EJ, Dixon AL, Döring A, Ehret G, Eyjolfsson GI, Farrall M, Forouhi NG, Friedrich N, Goessling W, Gudbjartsson DF, Harris TB, Hartikainen AL, Heath S, Hirschfield GM, Hofman A, Homuth G, Hyppönen E, Janssen HL, Johnson T, Kangas AJ, Kema IP, Kühn JP, Lai S, Lathrop M, Lerch MM, Li Y, Liang TJ, Lin JP, Loos RJ, Martin NG, Moffatt MF, Montgomery GW, Munroe PB, Musunuru K, Nakamura Y, O'Donnell CJ, Olafsson I, Penninx BW, Pouta A, Prins BP, Prokopenko I, Puls R, Ruokonen A, Savolainen MJ, Schlessinger D, Schouten JN, Seedorf U, Sen-Chowdhry S, Siminovitch KA, Smit JH, Spector TD, Tan W, Teslovich TM, Tukiainen T, Uitterlinden AG, Van der Klauw MM, Vasan RS, Wallace C, Wallaschofski H, Wichmann HE, Willemsen G, Würtz P, Xu C, Yerges-Armstrong LM; Alcohol Genome-wide Association (AlcGen) Consortium; Diabetes Genetics Replication and Meta-analyses (DIAGRAM+) Study; Genetic Investigation of Anthropometric Traits (GIANT) Consortium; Global Lipids Genetics Consortium; Genetics of Liver Disease (GOLD) Consortium; International Consortium for Blood Pressure (ICBP-GWAS); Meta-analyses of Glucose and Insulin-Related Traits Consortium (MAGIC), Abecasis GR, Ahmadi KR, Boomsma DI, Caulfield M, Cookson WO, van Duijn CM, Froguel P, Matsuda K, McCarthy MI, Meisinger C, Mooser V, Pietiläinen KH, Schumann G, Snieder H, Sternberg MJ, Stolk RP, Thomas HC, Thorsteinsdottir U, Uda M, Waeber G, Wareham NJ, Waterworth DM, Watkins H, Whitfield JB, Witteman JC, Wolffenbuttel BH, Fox CS, Ala-Korpela M, Stefansson K, Vollenweider P, Völzke H, Schadt EE, Scott J, Järvelin MR, Elliott P, Kooner JS. | |
| Nat Genet. 2011 Oct 16;43(11):1131-8. doi: 10.1038/ng.970. | |
| PMID: 22001757 [PubMed - indexed for MEDLINE] Free PMC Article | |
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| 8. | Next generation sequencing of pooled samples reveals new SNRNP200 mutations associated with retinitis pigmentosa. |
| Benaglio P, McGee TL, Capelli LP, Harper S, Berson EL, Rivolta C. | |
| Hum Mutat. 2011 Jun;32(6):E2246-58. doi: 10.1002/humu.21485. Epub 2011 Feb 24. | |
| PMID: 21618346 [PubMed - indexed for MEDLINE] | |
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| 9. | A missense mutation in PRPF6 causes impairment of pre-mRNA splicing and autosomal-dominant retinitis pigmentosa. |
| Tanackovic G, Ransijn A, Ayuso C, Harper S, Berson EL, Rivolta C. | |
| Am J Hum Genet. 2011 May 13;88(5):643-9. Epub 2011 May 5. | |
| PMID: 21549338 [PubMed - indexed for MEDLINE] Free PMC Article | |
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| 10. | Network-guided analysis of genes with altered somatic copy number and gene expression reveals pathways commonly perturbed in metastatic melanoma. |
| Valsesia A, Rimoldi D, Martinet D, Ibberson M, Benaglio P, Quadroni M, Waridel P, Gaillard M, Pidoux M, Rapin B, Rivolta C, Xenarios I, Simpson AJ, Antonarakis SE, Beckmann JS, Jongeneel CV, Iseli C, Stevenson BJ. | |
| PLoS One. 2011 Apr 8;6(4):e18369. | |
| PMID: 21494657 [PubMed - indexed for MEDLINE] Free PMC Article | |
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| 11. | PRPF mutations are associated with generalized defects in spliceosome formation and pre-mRNA splicing in patients with retinitis pigmentosa. |
| Tanackovic G, Ransijn A, Thibault P, Abou Elela S, Klinck R, Berson EL, Chabot B, Rivolta C. | |
| Hum Mol Genet. 2011 Jun 1;20(11):2116-30. Epub 2011 Mar 5. | |
| PMID: 21378395 [PubMed - indexed for MEDLINE] Free PMC Article | |
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| 12. | Ultra high throughput sequencing in human DNA variation detection: a comparative study on the NDUFA3-PRPF31 region. |
| Benaglio P, Rivolta C. | |
| PLoS One. 2010 Sep 29;5(9). doi:pii: e13071. | |
| PMID: 20927379 [PubMed - indexed for MEDLINE] Free PMC Article | |
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| 13. | Hundreds of variants clustered in genomic loci and biological pathways affect human height. |
| Lango Allen H, Estrada K, Lettre G, Berndt SI, Weedon MN, Rivadeneira F, Willer CJ, Jackson AU, Vedantam S, Raychaudhuri S, Ferreira T, Wood AR, Weyant RJ, Segrè AV, Speliotes EK, Wheeler E, Soranzo N, Park JH, Yang J, Gudbjartsson D, Heard-Costa NL, Randall JC, Qi L, Vernon Smith A, Mägi R, Pastinen T, Liang L, Heid IM, Luan J, Thorleifsson G, Winkler TW, Goddard ME, Sin Lo K, Palmer C, Workalemahu T, Aulchenko YS, Johansson A, Zillikens MC, Feitosa MF, Esko T, Johnson T, Ketkar S, Kraft P, Mangino M, Prokopenko I, Absher D, Albrecht E, Ernst F, Glazer NL, Hayward C, Hottenga JJ, Jacobs KB, Knowles JW, Kutalik Z, Monda KL, Polasek O, Preuss M, Rayner NW, Robertson NR, Steinthorsdottir V, Tyrer JP, Voight BF, Wiklund F, Xu J, Zhao JH, Nyholt DR, Pellikka N, Perola M, Perry JR, Surakka I, Tammesoo ML, Altmaier EL, Amin N, Aspelund T, Bhangale T, Boucher G, Chasman DI, Chen C, Coin L, Cooper MN, Dixon AL, Gibson Q, Grundberg E, Hao K, Juhani Junttila M, Kaplan LM, Kettunen J, König IR, Kwan T, Lawrence RW, Levinson DF, Lorentzon M, McKnight B, Morris AP, Müller M, Suh Ngwa J, Purcell S, Rafelt S, Salem RM, Salvi E, Sanna S, Shi J, Sovio U, Thompson JR, Turchin MC, Vandenput L, Verlaan DJ, Vitart V, White CC, Ziegler A, Almgren P, Balmforth AJ, Campbell H, Citterio L, De Grandi A, Dominiczak A, Duan J, Elliott P, Elosua R, Eriksson JG, Freimer NB, Geus EJ, Glorioso N, Haiqing S, Hartikainen AL, Havulinna AS, Hicks AA, Hui J, Igl W, Illig T, Jula A, Kajantie E, Kilpeläinen TO, Koiranen M, Kolcic I, Koskinen S, Kovacs P, Laitinen J, Liu J, Lokki ML, Marusic A, Maschio A, Meitinger T, Mulas A, Paré G, Parker AN, Peden JF, Petersmann A, Pichler I, Pietiläinen KH, Pouta A, Ridderstråle M, Rotter JI, Sambrook JG, Sanders AR, Schmidt CO, Sinisalo J, Smit JH, Stringham HM, Bragi Walters G, Widen E, Wild SH, Willemsen G, Zagato L, Zgaga L, Zitting P, Alavere H, Farrall M, McArdle WL, Nelis M, Peters MJ, Ripatti S, van Meurs JB, Aben KK, Ardlie KG, Beckmann JS, Beilby JP, Bergman RN, Bergmann S, Collins FS, Cusi D, den Heijer M, Eiriksdottir G, Gejman PV, Hall AS, Hamsten A, Huikuri HV, Iribarren C, Kähönen M, Kaprio J, Kathiresan S, Kiemeney L, Kocher T, Launer LJ, Lehtimäki T, Melander O, Mosley TH Jr, Musk AW, Nieminen MS, O'Donnell CJ, Ohlsson C, Oostra B, Palmer LJ, Raitakari O, Ridker PM, Rioux JD, Rissanen A, Rivolta C, Schunkert H, Shuldiner AR, Siscovick DS, Stumvoll M, Tönjes A, Tuomilehto J, van Ommen GJ, Viikari J, Heath AC, Martin NG, Montgomery GW, Province MA, Kayser M, Arnold AM, Atwood LD, Boerwinkle E, Chanock SJ, Deloukas P, Gieger C, Grönberg H, Hall P, Hattersley AT, Hengstenberg C, Hoffman W, Lathrop GM, Salomaa V, Schreiber S, Uda M, Waterworth D, Wright AF, Assimes TL, Barroso I, Hofman A, Mohlke KL, Boomsma DI, Caulfield MJ, Cupples LA, Erdmann J, Fox CS, Gudnason V, Gyllensten U, Harris TB, Hayes RB, Jarvelin MR, Mooser V, Munroe PB, Ouwehand WH, Penninx BW, Pramstaller PP, Quertermous T, Rudan I, Samani NJ, Spector TD, Völzke H, Watkins H, Wilson JF, Groop LC, Haritunians T, Hu FB, Kaplan RC, Metspalu A, North KE, Schlessinger D, Wareham NJ, Hunter DJ, O'Connell JR, Strachan DP, Wichmann HE, Borecki IB, van Duijn CM, Schadt EE, Thorsteinsdottir U, Peltonen L, Uitterlinden AG, Visscher PM, Chatterjee N, Loos RJ, Boehnke M, McCarthy MI, Ingelsson E, Lindgren CM, Abecasis GR, Stefansson K, Frayling TM, Hirschhorn JN. | |
| Nature. 2010 Oct 14;467(7317):832-8. Epub 2010 Sep 29. | |
| PMID: 20881960 [PubMed - indexed for MEDLINE] Free PMC Article | |
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| 14. | Nonsense mutations in FAM161A cause RP28-associated recessive retinitis pigmentosa. |
| Langmann T, Di Gioia SA, Rau I, Stöhr H, Maksimovic NS, Corbo JC, Renner AB, Zrenner E, Kumaramanickavel G, Karlstetter M, Arsenijevic Y, Weber BH, Gal A, Rivolta C. | |
| Am J Hum Genet. 2010 Sep 10;87(3):376-81. Epub 2010 Aug 12. | |
| PMID: 20705278 [PubMed - indexed for MEDLINE] Free PMC Article | |
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| 15. | Ultra high throughput sequencing excludes MDH1 as candidate gene for RP28-linked retinitis pigmentosa. |
| Rio Frio T, Panek S, Iseli C, Di Gioia SA, Kumar A, Gal A, Rivolta C. | |
| Mol Vis. 2009 Dec 8;15:2627-33. | |
| PMID: 20011630 [PubMed - indexed for MEDLINE] Free PMC Article | |
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| 16. | A single-base substitution within an intronic repetitive element causes dominant retinitis pigmentosa with reduced penetrance. |
| Rio Frio T, McGee TL, Wade NM, Iseli C, Beckmann JS, Berson EL, Rivolta C. | |
| Hum Mutat. 2009 Sep;30(9):1340-7. | |
| PMID: 19618371 [PubMed - indexed for MEDLINE] Free PMC Article | |
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| 17. | Mutation screening of the glutamate cysteine ligase modifier (GCLM) gene in patients with schizophrenia. |
| Butticaz C, Werge T, Beckmann JS, Cuénod M, Do KQ, Rivolta C. | |
| Psychiatr Genet. 2009 Aug;19(4):201-8. | |
| PMID: 19455074 [PubMed - indexed for MEDLINE] | |
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| 18. | PRPF31 alternative splicing and expression in human retina. |
| Tanackovic G, Rivolta C. | |
| Ophthalmic Genet. 2009 Jun;30(2):76-83. | |
| PMID: 19373678 [PubMed - indexed for MEDLINE] | |
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| 19. | The zinc transporter SLC39A13/ZIP13 is required for connective tissue development; its involvement in BMP/TGF-beta signaling pathways. |
| Fukada T, Civic N, Furuichi T, Shimoda S, Mishima K, Higashiyama H, Idaira Y, Asada Y, Kitamura H, Yamasaki S, Hojyo S, Nakayama M, Ohara O, Koseki H, Dos Santos HG, Bonafe L, Ha-Vinh R, Zankl A, Unger S, Kraenzlin ME, Beckmann JS, Saito I, Rivolta C, Ikegawa S, Superti-Furga A, Hirano T. | |
| PLoS One. 2008;3(11):e3642. Epub 2008 Nov 5. Erratum in: PLoS One. 2008;3(11). doi: 10.1371/annotation/a6c35a12-e8eb-43a0-9d00-5078fa6da1bb. | |
| PMID: 18985159 [PubMed - indexed for MEDLINE] Free PMC Article | |
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| 20. | Two trans-acting eQTLs modulate the penetrance of PRPF31 mutations. |
| Rio Frio T, Civic N, Ransijn A, Beckmann JS, Rivolta C. | |
| Hum Mol Genet. 2008 Oct 15;17(20):3154-65. Epub 2008 Jul 18. | |
| PMID: 18640990 [PubMed - indexed for MEDLINE] Free Article | |
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| 21. | Premature termination codons in PRPF31 cause retinitis pigmentosa via haploinsufficiency due to nonsense-mediated mRNA decay. |
| Rio Frio T, Wade NM, Ransijn A, Berson EL, Beckmann JS, Rivolta C. | |
| J Clin Invest. 2008 Apr;118(4):1519-31. | |
| PMID: 18317597 [PubMed - indexed for MEDLINE] Free PMC Article | |
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| 22. | Mutation screening of the peropsin gene, a retinal pigment epithelium specific rhodopsin homolog, in patients with retinitis pigmentosa and allied diseases. |
| Rivolta C, Berson EL, Dryja TP. | |
| Mol Vis. 2006 Dec 5;12:1511-5. | |
| PMID: 17167409 [PubMed - indexed for MEDLINE] Free Article | |
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| 23. | Variation in retinitis pigmentosa-11 (PRPF31 or RP11) gene expression between symptomatic and asymptomatic patients with dominant RP11 mutations. |
| Rivolta C, McGee TL, Rio Frio T, Jensen RV, Berson EL, Dryja TP. | |
| Hum Mutat. 2006 Jul;27(7):644-53. | |
| PMID: 16708387 [PubMed - indexed for MEDLINE] | |
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| 24. | Comprehensive screening of the USH2A gene in Usher syndrome type II and non-syndromic recessive retinitis pigmentosa. |
| Seyedahmadi BJ, Rivolta C, Keene JA, Berson EL, Dryja TP. | |
| Exp Eye Res. 2004 Aug;79(2):167-73. | |
| PMID: 15325563 [PubMed - indexed for MEDLINE] | |
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| 25. | Essential Bacillus subtilis genes. |
| Kobayashi K, Ehrlich SD, Albertini A, Amati G, Andersen KK, Arnaud M, Asai K, Ashikaga S, Aymerich S, Bessieres P, Boland F, Brignell SC, Bron S, Bunai K, Chapuis J, Christiansen LC, Danchin A, Débarbouille M, Dervyn E, Deuerling E, Devine K, Devine SK, Dreesen O, Errington J, Fillinger S, Foster SJ, Fujita Y, Galizzi A, Gardan R, Eschevins C, Fukushima T, Haga K, Harwood CR, Hecker M, Hosoya D, Hullo MF, Kakeshita H, Karamata D, Kasahara Y, Kawamura F, Koga K, Koski P, Kuwana R, Imamura D, Ishimaru M, Ishikawa S, Ishio I, Le Coq D, Masson A, Mauël C, Meima R, Mellado RP, Moir A, Moriya S, Nagakawa E, Nanamiya H, Nakai S, Nygaard P, Ogura M, Ohanan T, O'Reilly M, O'Rourke M, Pragai Z, Pooley HM, Rapoport G, Rawlins JP, Rivas LA, Rivolta C, Sadaie A, Sadaie Y, Sarvas M, Sato T, Saxild HH, Scanlan E, Schumann W, Seegers JF, Sekiguchi J, Sekowska A, Séror SJ, Simon M, Stragier P, Studer R, Takamatsu H, Tanaka T, Takeuchi M, Thomaides HB, Vagner V, van Dijl JM, Watabe K, Wipat A, Yamamoto H, Yamamoto M, Yamamoto Y, Yamane K, Yata K, Yoshida K, Yoshikawa H, Zuber U, Ogasawara N. | |
| Proc Natl Acad Sci U S A. 2003 Apr 15;100(8):4678-83. Epub 2003 Apr 7. | |
| PMID: 12682299 [PubMed - indexed for MEDLINE] Free PMC Article | |
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| 26. | Evaluation of the ELOVL4 gene in patients with autosomal recessive retinitis pigmentosa and Leber congenital amaurosis. |
| Rivolta C, Ayyagari R, Sieving PA, Berson EL, Dryja TP. | |
| Mol Vis. 2003 Feb 18;9:49-51. | |
| PMID: 12592226 [PubMed - indexed for MEDLINE] Free Article | |
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| 27. | Paternal uniparental heterodisomy with partial isodisomy of chromosome 1 in a patient with retinitis pigmentosa without hearing loss and a missense mutation in the Usher syndrome type II gene USH2A. |
| Rivolta C, Berson EL, Dryja TP. | |
| Arch Ophthalmol. 2002 Nov;120(11):1566-71. | |
| PMID: 12427073 [PubMed - indexed for MEDLINE] | |
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| 28. | Barrier to autointegration factor interacts with the cone-rod homeobox and represses its transactivation function. |
| Wang X, Xu S, Rivolta C, Li LY, Peng GH, Swain PK, Sung CH, Swaroop A, Berson EL, Dryja TP, Chen S. | |
| J Biol Chem. 2002 Nov 8;277(45):43288-300. Epub 2002 Sep 4. | |
| PMID: 12215455 [PubMed - indexed for MEDLINE] Free Article | |
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| 29. | Retinitis pigmentosa and allied diseases: numerous diseases, genes, and inheritance patterns. |
| Rivolta C, Sharon D, DeAngelis MM, Dryja TP. | |
| Hum Mol Genet. 2002 May 15;11(10):1219-27. Review. Erratum in: Hum Mol Genet. 2003 Mar 1;12(5):583-4. | |
| PMID: 12015282 [PubMed - indexed for MEDLINE] Free Article | |
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| 30. | Novel frameshift mutations in CRX associated with Leber congenital amaurosis. |
| Rivolta C, Peck NE, Fulton AB, Fishman GA, Berson EL, Dryja TP. | |
| Hum Mutat. 2001 Dec;18(6):550-1. | |
| PMID: 11748859 [PubMed - indexed for MEDLINE] | |
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| 31. | Dominant Leber congenital amaurosis, cone-rod degeneration, and retinitis pigmentosa caused by mutant versions of the transcription factor CRX. |
| Rivolta C, Berson EL, Dryja TP. | |
| Hum Mutat. 2001 Dec;18(6):488-98. Review. | |
| PMID: 11748842 [PubMed - indexed for MEDLINE] | |
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| 32. | Missense mutation in the USH2A gene: association with recessive retinitis pigmentosa without hearing loss. |
| Rivolta C, Sweklo EA, Berson EL, Dryja TP. | |
| Am J Hum Genet. 2000 Jun;66(6):1975-8. Epub 2000 Apr 20. | |
| PMID: 10775529 [PubMed - indexed for MEDLINE] Free PMC Article | |
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| 33. | Bacillus subtilis contains two small c-type cytochromes with homologous heme domains but different types of membrane anchors. |
| Bengtsson J, Rivolta C, Hederstedt L, Karamata D. | |
| J Biol Chem. 1999 Sep 10;274(37):26179-84. | |
| PMID: 10473570 [PubMed - indexed for MEDLINE] Free Article | |
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| 34. | Genetic and physical maps of the Bacillus subtilis chromosome. |
| Rivolta C, Pagni M. | |
| Genetics. 1999 Apr;151(4):1239-44. | |
| PMID: 10101153 [PubMed - indexed for MEDLINE] Free PMC Article | |
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| 35. | Subunit II of Bacillus subtilis cytochrome c oxidase is a lipoprotein. |
| Bengtsson J, Tjalsma H, Rivolta C, Hederstedt L. | |
| J Bacteriol. 1999 Jan;181(2):685-8. | |
| PMID: 9882689 [PubMed - indexed for MEDLINE] Free PMC Article | |
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| 36. | The product of the yvoC (gerF) gene of Bacillus subtilis is required for spore germination. |
| Robinson C, Rivolta C, Karamata D, Moir A. | |
| Microbiology. 1998 Nov;144 ( Pt 11):3105-9. | |
| PMID: 9846746 [PubMed - indexed for MEDLINE] Free Article | |
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| 37. | A 35.7 kb DNA fragment from the Bacillus subtilis chromosome containing a putative 12.3 kb operon involved in hexuronate catabolism and a perfectly symmetrical hypothetical catabolite-responsive element. |
| Rivolta C, Soldo B, Lazarevic V, Joris B, Mauël C, Karamata D. | |
| Microbiology. 1998 Apr;144 ( Pt 4):877-84. | |
| PMID: 9579062 [PubMed - indexed for MEDLINE] Free Article | |
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| 38. | A novel protein kinase that controls carbon catabolite repression in bacteria. |
| Reizer J, Hoischen C, Titgemeyer F, Rivolta C, Rabus R, Stülke J, Karamata D, Saier MH Jr, Hillen W. | |
| Mol Microbiol. 1998 Mar;27(6):1157-69. | |
| PMID: 9570401 [PubMed - indexed for MEDLINE] | |
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| 39. | The complete genome sequence of the gram-positive bacterium Bacillus subtilis. |
| Kunst F, Ogasawara N, Moszer I, Albertini AM, Alloni G, Azevedo V, Bertero MG, Bessières P, Bolotin A, Borchert S, Borriss R, Boursier L, Brans A, Braun M, Brignell SC, Bron S, Brouillet S, Bruschi CV, Caldwell B, Capuano V, Carter NM, Choi SK, Codani JJ, Connerton IF, Danchin A, et al. | |
| Nature. 1997 Nov 20;390(6657):249-56. | |
| PMID: 9384377 [PubMed - indexed for MEDLINE] | |
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