• Non ci sono risultati.

RIFERIMENTI BIBLIOGRAFICI

N/A
N/A
Protected

Academic year: 2021

Condividi "RIFERIMENTI BIBLIOGRAFICI"

Copied!
10
0
0

Testo completo

(1)
(2)

• Alvares K., Dixit S. N., Lux E., Barss J. & Veis A. (2007). The Proteome of the Developing Tooth of the Sea Urchin, Lythechinus variegates: Mortalin is a Constituent of the Developing Cell Syncytium. J. Exp. Zool. 308B:357-370

• Bagun҃a J. (1973). Estudios citotaxonomicos, ecologicos, e histofisiologia de la regulation morfogenetica durante el crecimiento y la re generation de la raza asexuada de la planaria Dugesia mediterranea n. sp. (Turbellaria, Trioladida, Paludicola). Genetics, Universitad de Barcelona

• Bagun҃a J. (1974). Dramatic mitotic response in planarians after feeding, and a hypothesis for the control mechanism. J. Exp. Zool. 190:117-22

• Bagun҃a J. (1976). Mitosis in the intact and regenerating planarian Dugesia

mediterranea n. sp. I Mitotic studies during growth, feeding and starvation. J. Exp. Zool. 195:65-80

• Bagun҃a J., R. Romero, Garcia-Fernàndez J., Bueno D., Mun҃ioz-Mármol A. M.,

Bayascas-Ramírez J. R., Casali A. (1994). Regeneration and pattern formation in

planarians: cells, molecules and genes. Zool. Sci. 11:781-795

• Bagun҃a J., Salò E. & Auladell C. (1989). Regeneration and pattern formation in planarians III. Evidence that neoblasts are totipotent stem cells and the source of blastema cells. Development 107:77-86

• Bardeen C. R. (1991). On the physiology of the Planaria maculate with especial reference to the phenomena of regeneration. American Journal of Physiology. 5:1-55

• Bhattacharyya T., Karnezis A. N., Murphy S. P., Hoang T., Freeman B. C.,

Phillips B. & Morimoto R. I. (1995). Cloning and subcellular localization of

human mitochondrial hsp70. J. Biol. Chem. 270:1705-1710

• Böttger S., Jerszyk E., Low B. & Walker C. (2008). Genotoxic Stress-Induced Expression of p53 and Apoptosis in Leukemic Clam Hemocytes with Cytoplasmically Sequestered p53. Cancer Res. 68

• Cebrià F. & Newmark P. A. (2005). Planarian homologs of netrin and netrin receptor are required for proper regeneration of the central nervous system and the maintenance of nervous system architecture. Development 132:3691-703

(3)

• Chandobois R. (1980). The dynamics of wound closure and its role in the programming of planarian regeneration II. Distalitation. Dev. Growth Differ. 22:694-704

• Coward S. J. (1974). Chromatoid Bodies in Somatic Cells of the Planarian: Observations on Their Behaviour during Mitosis. The Anatomical Record 180,3:533-546

• Curtis W. (1902). The life history, the normal fission, and the reproductive organs of Planarian maculate. Proc. Boston Society of Nat. Hist. 30:515-549

• Deocaris C. C., Kaul S. C. & Wadhwa R. (2006a). On the brotherhood of the mitochondrial chaperones mortalin and heat shock protein 60. Cell Stress Chaperones 11:116-128

• Deocaris C. C., Yamasaki K., Kaul S. C. & Wadhwa R. (2006c). Structural and functional differences between mouse mot-1 and mot-2 proteins that differ in two amino acids. Ann. NY Acad. Sci. 1067:220-223

• Dubois F. (1949). Contribution á l’etude de la migration des cellules de règènèration chez les planaries dulcicoles. Bull. Biol. Fr. Belg. 83:213-283

• Egger B., Gschwentner R. & Rieger R. (2007). Free-living flatworms under the knife: past and present. Dev. Genes Evol. 217:89-104

• Geissler A., Rassow J., Pfanner N. & Woos W. (2001). Mitochondrial import driving forces: enhanced trapping by matrix Hsp70 stimulates traslocation and reduces the membrane potential dependence of loosely folded preproteins. Mol. Cell Biol. 21:7097-7104

• Glick B. S. (1995). Pathways and energetics of mitochondrial protein import in

Saccharomyces cerevisiae. Method Enzymol. 260:224-231

• González-Estevez C., Felix D. A., Aboobaker A. A. & Salò E. (2007). Gtdap-1 promotes autophagy and is required for planarian remodeling during regeneration and starvation. Proc. Natl. Acad. Sci. USA 104:13373-8

• González-Estevez C., Momose T., Gehring W. J. & Salò E. (2003). Transgenic planarian lines obtained by electroporation using trasposon-derived vectors and an eye-specific GFP marker. Proc. Natl. Acad. Sci. USA 100:14046-51

(4)

• Grasso M. (1959). Fenome rigenerativi e apparato genital in Dugesia lucubris. Boll. Zool. 26:523-527

• Guo T., Peters A. H. & Newmark P. A. (2006). A Bruno-like gene is required for stem cell maintenance in planarians. Dev. Cell 11:159-69

• Handberg-Thorsager M. & Salò E. (2007). The planarian nanos-like gene

Smednos is expressed in germline and eye precursor cells during development and regeneration. Dev. Genes Evol. 217:403-11

• Hartl F. U., Martin J. & Neupert W (1992). Protein folding in the cell: the role of molecular chaperones Hsp70 and Hsp60. Annu. Rev. Biophys. Biomol. Struct. 21:293-322

• Hayashi T., Asami M., Higochi S., Shibata N. & Agata K. (2006). Isolation of planarian X-ray-sensitive stem cells by fluorescence-activated cell sorting. Dev. Growth Differ. 48:371-80

• Higuchi S., Hayashi T., Hori I., Shibata N., Sagamoto H. & Agata K. (2007). Characterization and chategorization of fluorescences activated cell sorted planarian stem cells by ultrastructural analysis. Dev. Growth Differ. 49:571-81

• Horst M., Oppliger W., Rospert S., Schonfeld H. J., Schatz G. & Azem A. (1997). Sequential action of two hsp70 complexes during protein import into mitochondrial. EMBO J. 16:1842-1849

• Hunt C. & Calderwood S. (1990). Characterization and sequence of a mouse hsp70 gene and its expression in mouse cell lines. Gene 87:199-204

• Hunt C. R., Gasser D. L., Chaplin D. D., Pierce J. C. & Kozak C. A. (1993). Chromosomal localization of five murine HSP70 gene family members: Hsp70-1,

Hsp70-2, Hsp70-3, Hsc70t, and Grp78. Genomics 16:193-198

• Kato K., Orii H., Watanabe K. & Agata K. (2001). Dorsal and ventral positional cues require for the onset off planarian regeneration may reside in differentiated cells. Dev. Biol. 233:109-21

• Kaul S. C., Deocaris C. C. & Wadhwa R. (2007). Three faces of mortalin: A housekeeper, guardian and killer. Exp. Ger. 42:263-274

(5)

• Kaul S. C., Duncan E. L., Englezou A., Takano S., Reddel R. R., Mitsui Y. &

Wadhwa R. (1998). Malignant transformation of NIH3T3 cells by overexpression

of mot-2 protein. Oncogene 17:907-911

• Kaul S. C., Duncan E., Sugihara T., Reddel R. R., Mitsui Y. & Wadhwa R. (2000a). Structurally and functionally distinct mouse hsp70 family members Mot-1 and Mot-2 proteins are encoder by two alleles. DNA Res. 7:229-231

• Kaul S. C., Wadhwa R., Komatsu Y., Sugimoto Y. & Mitsui Y. (1993). On the cytosolic and perinuclear mortalin: an insight by heat shock. Biochem. Biophys. Res. Commun. 193:348-355

• Koehler C. M. (2004). New developments in mitochondrial assembly. Annu. Rev. Cell Dev. Biol. 20:309-335

• Langer T. & Neupert W. (1991). Heat shock proteins hsp60 and hsp70: their roles in folding, assembly and membrane traslocation of proteins. Curr. Top. Microbiol. Immunol. 167:3-30

• Lender T. & Gabriel A. (1965). Neoblastas Labelled with Tritiated Uridine Migrate and Construct and Regeneration Blastema in Fresh-Water Planarian. C. R. Hebd. Seances. Acad. Sci. 260:4095-4097

• Mahlke K., Pfanner N., Martin J., Horwich A. L., Hartl F. U. & Neupert W. (1990). Sorting pathways of mitochondrial inner membrane proteins. Eur. J. Biochem. 192:551-555

• Mannini, L., Rossi, L., Deri, P., Gremigni, V., Salvetti, A., Salo, E. and

Batistoni, R. (2004). Djeyes absent (Djeya) controls prototypic planarian eye

regeneration by cooperating with the transcription factor Djsix-1. Dev Biol 269:346-59

• Mineta K., Nakazawa M., Cebrià F., Ikeo K., Agata K. & Gojobori T. (2003). Origin and evolutionary process of the CNS elucidated by comparative genomics analysis of planarian ESTs. Proc. Natl. Acad. Sci. U.S.A. 100 (13): 7666-7671 • Mioara M. (2004). Differential tissue development during embryogenesis and

(6)

• Mizukoshi E., Suzuki M., Loupatov A., Urunu T., Hayashi H., Misono T., Kaul

S. C., Wadhwa R. & Imamura T. (1999). Fibroblast growth factor-1 interacts with

the glucose-regulated protein GRP75/mortalin. Biochem. J. 2:461-466

• Mizukoshi E., Suzuki M., Misono T., Loupatov A., Munekata E., Kaul S. C.,

Wadhwa R. & Imamura T. (2001). Cell-cycle dependent tyrosine phosphorylation

on mortalin regulates its interaction with fibroblast growth factor-1. Biochem. Biophys. Res. Commun. 280:1203-1209

• Morgan T. H. (1901). Growth and Regeneration in Planaria lugubris. Arch. Entw. Mech. Org. 13:179-212

• Morita M. & Best J. B. (1984). Electron microscopic studies of planarian regeneration IV. cell division of neoblasts in Dugesia dorotochepala. J. Exp. Zool. 229:425-436

• Mukhopadhyay I., Nazir A., Safena D. K. & Chowdhuri D. K. (2003). Heat shock response: hsp70 in environmental monitoring. J. Biochem. Mol. Toxicol. 17:249-254

• Newmark P. A. & Sánchez Alvarado A. (2000). Bromodeoxyuridine specifically labels the regenerative stem cells of planarians. Dev. Biol. 220:142-53

• Newmark P. A., Reddien P. W., Cebrià F. & Sánchez Alvarado A. (2003). Ingestion of bacterially espressed double-stranded RNA inhibits gene expression in planarians. Proc. Natl. Acad. Sci. USA 100 Suppl 1:11861-5

• Nimeth K. T., Mahlknecht M., Mezzanato A., Peter R., Rieger R. & Ladurner

P. (2004). Stem cell dynamics dutring growth, feeding and starvation in the basal

flatworm Macrostotum sp. (Plathelminthes). Dev. Dyn. 230:91-09

• Nogi T. e Levin M. (2005). Characterization of innexin gene expression and functional roles of gap-junctional communication in planaria regeneration. Devel. Biol. 287:314-355

• Nollen E. A. & Morimoto R. I. (2002). Chaperoning signaling pathway: molecular chaperones as stress-sensing “heat shock” proteins. J. Cell Sci. 115:2809-2816 • Orii H., Mochii M. & Watanabe K. (2003). A simple “soaking method” for RNA

(7)

• Orii H., Sakurai T. & Watanabe K. (2005). Distribution of the stem cells (neoblasts) in the planarian Dugesia japonica. Dev. Genes Vol. 215:143-57

• Oviedo N. J. & Levin M. (2007). smedinx-11 is a planarian stem cell gap junction gene required for regeneration and homeostasis. Development 134:3121-31

• Pelletteri J. & Sánchez Alvarado A. (2007). Cell Turnover and Adult Tissue Homeostasis: From Humans to Planarians. Annu. Rev. Genet. 41:43-105

• Perry M. D., Adjame L., Shtang S. & Moran L. A. (1994). Structure and expression of an inducible hsp70-encoding gene from Mus musculus. Gene 146:273-278

• Poindexter B. J., Pereira-Smith O., Wadhwa R., Buja L. M. & Bick R. J. (2002). 3D reconstruction and localization of mortalin by deconvolution microscopy. Micros. Anal. 89:21-23

• Ran Q., Wadhwa R., Kawai R., Kaul S. C., Sifers R. N., Bick R. J., Smith J. R.

& Pereira-Smith O. M. (2000). Extramitochondrial localization of mortalin/mthsp70/PBP74/GRP75. Biochem. Biophys. Res. Commun. 275:174-179 • Randolf H. (1892). The regeneration of the tail in Lumbriculus. J. Morphol.

7,3:317-344

• Reddien P. W., Bermange A. L., Murfitt K. J., Jennings J. R. & Sánchez

Alvarado A. (2005). Identification of genes needed for regeneration, stem cell

function, and tissue homeostasis by systematic gene perturbation in planarian. Dev. Cell 8:635-49

• Rehling P., Brandner K. & Pfanner N. (2004). Mitochondrial import and the twin-pore translocase. Nat. Rev. Mol. Cell Biol. 5:519-530

• Rieger R. M., Tyler S., Smith III J. P. S., Rieger G. E. (1991). Microscopic Anatomy of Invertebrates (Chap. 2, Plathyhelmintes: Turbellaria). Wiles, New York • Robb S. M., Ross E. & Sánchez Alvarado A. (2008). SmedGd: the Schmidtea

mediterranea genome database. Nucleic Acids Res 36:D599-606

• Romero R. & Bagun҃a J. (1981). Quantitative analysis of cell types during growth, degrowth and regenration in the planarians Dugesia mediterranea and Dugesia

(8)

• Romero R., Bueno D., Sumoy L., Soriano M. A., Bagun҃a J. (1991). Monoclonal antibodies as markers of specific cell types and regional antigens in the freshwater planaria Dugesia (G) tigrina. Hydrobiologia 227:73-79

• Rossi L., Salvetti A., Lena A., Batistoni R., Deri P., Pugliesi C., Loreti E. &

Gremigni V. (2006). DjPiwi-1, a member of the PAZ-Piwi gene family, defines a

subpopulation of planarian stem cells. Dev. Genes Evol. 216:335-46

• Rossi L., Salvetti A., Marincola F. M., Lena A., Deri P., Mannini L., Batistoni

R., Wang E. & Gremigni V.g (2007). Deciphering the molecular machinery of

stem cells: a lock at the neoblast gene expression profile. Genome Biol. 8-R62 • Sacht G., Brigelius-Flohe R., Kiess M., Sztajer H. & Flohe L. (1999).

ATP-sensitive association of mortalin with the IL-1 receptor type I. Biofactors 9:49-60 • Salò E. & Bagun҃a J. (1984). Regeneration and pattern formation in planarians I.

The pattern of mitosis in anterior and posterior regeneration in Dugesia (G) tigrina, and a new proposal for blastema formation. J. Embryol. Exp. Morphol. 83:63-80 • Salò E. (1984). Formatión del blastema i re-specificatió del patró durant la

regeneratió de les planarie Dugesia (S) mediterranea i Dugesia (G) tigrina: analisi morfològica, cellular i biochimíca (PhD Thesis). Genetics, Universitat de Barcelona 312p

• Salvetti A., Rossi L., Deri P. & Batistoni R. (2000). An MCM2-related gene is espresse in proliferating cells of intact and regenerating planarians. Dev. Dyn. 218:603-14

• Salvetti A., Rossi L., Lena A., Batistoni R., Deri P., Rainaldi G., Locci M. T.,

Evagenlista M. & Gremigni V. (2005). DjPum a homologue of Drosophila Pumilio, is essential to planarian stem cell maintenance. Development 132:1863-74 • Sánchez Alvarado A. & Newmark P. A. (1999). Double-stranded RNA

specifically disrupts gene expression during planarian re generation. Proc. Natl. Acad. Sci. USA 96:5049-54

• Sato K., Shibata N., Orii H., Amikura R., Sakurai T., Agata K., Kobayaski S.

& Watanabe K. (2006). Identification and origino f the germline stem cells as

(9)

• Scott J. C. & McManus D. P. (1999). Identification of novel 70-kDa heat shock protein-encoding cDNAs from Schistosoma japonicum. Intern. J. Paras. 29:437-444 • Shibata N., Umesono Y., Orii H., Sakurai T., Watanabe K. & Agata K. (1999).

Expression of vasa (vas)-related genes in germline cells and totipotent somatic stem cells of planarians. Dev. Biol. 206:73-87

• Strub A., Lim J. H., Pfanner N. & Voos W. (2000). The mitochondrial protein import motor. Biol. Chem. 381:943-949

• Takano S., Wadhwa R., Mitsui Y. & Kaul S. C. (2001). Identification and characterization of molecular interactions between glucose-related proteins (GRPs) mortalin/GRP75/peptide-binding protein 74 (PBP74) and GRP94. Biochem. J. 357: 393-398

• Umesono Y., Watanabe K. & Agata K. (1997). A planarian orthopedia homologue is specifically express in the branch region of both the mature and regenerating brain. Dev. Growth Differ. 39:723-07

• Voos W., Von Ahsen O., Muller H., Guiard B., Rassow J. & Pfanner N. (1996). Differential requirement for the mitochondrial Hsp70-Tim44 complex in unfolding and traslocation of preproteins. EMBO J. 15:2668-2677

• Wadhwa R., Kaul S. C., Ikawa Y. & Sugimoto Y. (1993a). Identification of a novel member of mouse hsp70 family. Its association with cellular mortal phenotype. J. Biol. Chem. 268:6615-6621

• Wadhwa R., Kaul S. C., Mitsui Y. & Sugimoto Y. (1993b). Differential subcellular distribution of mortalin in mortal and immortal mouse and human fibroblast. Exp. Cell Res. 207:442-448

• Wadhwa R., Kaul S. C., Sugimoto Y. & Mitsui Y. (1993c). Induction of cellular senescence by transfection of cytosolic mortalin cDNA in NIH3T3 cells. J. Biol. Chem. 268:22239-22242

• Wadhwa R., Taira K. & Kaul S. C. (2002a). An Hsp70 family chaperone, mortalin/mthsp70/PBP74/Grp75: what, when, and there? Cell Stress Chaperones 7:309-316

(10)

• Walker C., Böttger S. & Low B. (2006). Mortalin-Base Cytoplasmic Sequestration of p53 in a Nonmammalian Cancer Model. Amer. J. of Path. Vol.168 No. 5

• Walker C., Bottger S. & Low B. (2006). Mortalin-based cytoplasmic sequestration of p53 in a nonmammalian cancer model. Am. J. Pathol. 168:1526-1530

• Wang Y., Zayas R. M., Guo T. & Newmark P. A. (2007). nanos function is essential for development and regeneration of planarian germ cells. Proc. Natl. Acad. Sci. USA 104:5901-06

• Wiedemann N., Frazier A. E. & Pfanner N. (2004). The protein import machinery of mitochondria. J. Biol. Chem. 279:14473-14476

• Yamamoto H., Momose T., Yatsukawa Y., Ohshima C., Ishikawa D., Sato T.,

Tamura Y., Ohwa Y & Endo T. (2005). Identification of a novel member of yeast

mitochondrial Hsp70-associated motor and chaperone proteins that facilities proteins that facilities protein trans location across the inner membrane. FEBS Lett. 579:507-511

• Yoshida-Kashikawa M., Shibata N., Takechi K. & Agata K. (2007). DjCBC-1, a conserved DEAD box RNA elicase of the RCK/p54/Me31B family, is a component of RNA-protein complexes in planarian stem cells and neurons. Dev. Dyn. 236:3436-3450

Riferimenti

Documenti correlati

In the relapse sample, there is complete loss of heterozygosity (LOH) without a change in the copy number suggesting UPD. B ) FISH analysis with the chromosome 13q14 LSI

Il vescovo di Ivrea, che era intervenuto all’assemblea conciliare sui temi della fede, della condotta dei chierici e della Chiesa, si segnalò tra i padri che si dichiararono

Altogether, the effects of morphological cueing, semantic impairment (indexed by noun comprehension) and grammatical impairment in determining generalization after verb therapies

We present an extensive study of the Eulerian distribution on the set of self evacuated involutions, namely, involutions corresponding to standard Young tableaux that are fixed

Santi Albanese e Gaetano Gulino Carmen Andriani Walter Angonese Anselmi&Associati Arrigoni architetti Olivo Barbieri Barozzi / Veiga Gabriele Bartocci Enrico Bordogna

This innovative and counterintuitive result suggest that (i) investing in trans- mission network is firstly useful in order to eliminate congestions; (ii) eliminating

Protecting cultural heritage from water-soil interaction related threats is a current issue and the prediction of the effects of slope displacements on buildings is very

Given a set of relaxed plans, the proposed algorithm for plan merging POMer X incrementally extracts actions from the input plans and greedily adds an action start point a or an