190 resultados para genet


Relevância:

10.00% 10.00%

Publicador:

Resumo:

‘Snap’ deploys the queer cliché of becoming-sailor as a trope for recognition in the amorous encounter and literalises the ‘copycat’ as its catalyst. As Girard argues (1973), the human is foremost mimetic: this story makes its claim for originality and authenticity of connection through the playful recycling of cliché.‘Snap’ eschews the relative affectlessness of some metafiction by staging an amorous approach under the shadow of mortality. It exploits the liminal moment of modernist short fiction to summon the ‘manifold’ of experience. Here, love opens a space of intertextual esonance (Costello 2007), including motifs of Genet (masquerade), Duras (haunting) and Maurice Blanchot (the infinite approach), by writing the threshold of encounter as the intensive silence of wond

Relevância:

10.00% 10.00%

Publicador:

Resumo:

A possible association between apolipoprotein E polymorphisms and age-related macular degeneration has been investigated numerous times, with conflicting results. A previous analysis pooling results from four studies (Schmidt et al., Ophthalmic Genet 2002;23:209-23) suggested an association, but those investigators did not document allele frequencies, the magnitude of the association, or the possible genetic mode of action. Thus, the authors searched MEDLINE from 1966 to December 2005 for any English-language studies reporting genetic associations. Data and study quality were assessed in duplicate. Pooling was performed while checking for heterogeneity and publication bias. Frequencies of the E2 and E4 alleles in Caucasians were approximately 8% and 15%, respectively. Allele- and genotype-based tests of association indicated a risk effect of up to 20% for E2 and a protective effect of up to 40% for E4. E2 appeared to act in a recessive mode and E4 in a dominant mode. There appears to be a differential effect of the E2 and E4 alleles on the risk of age-related macular degeneration, although the possibility of survivor bias needs to be ruled out more definitively.

Relevância:

10.00% 10.00%

Publicador:

Resumo:

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Relevância:

10.00% 10.00%

Publicador:

Resumo:

We report on four Brazilian patients with, among other signs, cleft lip and palate, dental anomalies, ectropion of the lower eyelids, euryblepharon, and lagophthalmia, Two were sporadic cases and two were familial cases, a mother and her equally affected son, Recently, the reports with different combination of these signs were reviewed by Gorlin et al, [1996; Am J Med Genet 65:109-112] and named blepharo-cheilo-dontic (BCD) syndrome, Variable expressivity and autosomal dominant inheritance were observed. (C) 1998 Wiley-Liss, Inc.

Relevância:

10.00% 10.00%

Publicador:

Resumo:

Purpose: Interferon regulatory factor 6 encodes a member of the IRF family of transcription factors. Mutations in interferon regulatory factor 6 cause Van der Woude and popliteal pterygium syndrome, two related orofacial clefting disorders. Here, we compared and contrasted the frequency and distribution of exonic Mutations in interferon regulatory factor 6 between two large geographically distinct collections of families with Van der Woude and between one collection of families with popliteal pterygium syndrome. Methods: We performed direct sequence analysis of interferon regulatory factor 6 exons oil samples from three collections, two with Van der Woude and one with popliteal pterygium syndrome. Results: We identified mutations in interferon regulatory factor 6 exons in 68% of families in both Van der Woude collections and in 97% of families with popliteal pterygium syndrome. In sum, 106 novel disease-causing variants were found. The distribution of mutations in the interferon regulatory factor 6 exons in each collection was not random; exons 3, 4, 7, and 9 accounted for 80%. In the Van der Woude collections, the mutations were evenly divided between protein truncation and missense, whereas most mutations identified in the popliteal pterygium syndrome collection were missense. Further, the missense mutations associated with popliteal pterygium syndrome were localized significantly to exon 4, at residues that are predicted to bind directly to DNA. Conclusion: The nonrandom distribution of mutations in the interferon regulatory factor 6 exons suggests a two-tier approach for efficient mutation screens for interferon regulatory factor 6. The type and distribution of mutations are consistent with the hypothesis that Van der Woude is caused by haploinsufficiency of interferon regulatory factor 6. Oil the other hand, the distribution of popliteal pterygium syndrome-associated mutations suggests a different, though not mutually exclusive, effect oil interferon regulatory factor 6 function. Genet Med 2009:11(4):241-247.

Relevância:

10.00% 10.00%

Publicador:

Resumo:

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Relevância:

10.00% 10.00%

Publicador:

Resumo:

Speech/language disorders are common in the fragile X syndrome. [Howard-Peebles, 1979: Am J Hom Genet 31:214-222; Renier et al., 1983: J Ment Defic Res 27:51-59; Sparks, 1984: Birth Defects and Speech-Language Disorders, pp, 39-43; Hanson et al., 1986: Am J Med Genet 23:195-206]. Verbal paraphasias have been considered a rare feature and word-finding difficulties have seldom been reported. Here we report on ten Brazilian patients who were evaluated for speech/language disturbances and found that word-finding difficulties were present in 50% of the cases, which is a slightly higher frequency than that of clear dyspraxia. We suggest, therefore, that word-finding difficulties and verbal dyspraxia can be a common feature within the spectrum of this syndrome. Additional speech findings are discussed. (C) 1995 Wiley-Liss, Inc.

Relevância:

10.00% 10.00%

Publicador:

Resumo:

In order to develop an efficient and low-cost technique for obtaining bird chromosome preparations, and to adapt the cytogenetic process of bird sexing for general use at zoos and breeding farms with the technical support of cytogenetics laboratories, we tested variants of the technique described by Giannoni et al. (Genet. Sel. Evol. 23: 123-125, 1991), based on the utilization of cellular material from growing feather pulp cultured in complete medium for six hours. Hanks' saline solution gave satisfactory performance as a substitute for complete medium, with no need to use PHA, serum of collagenase, when utilized in material obtained from feather pulp of Amazona amazonica (Psittacidae).

Relevância:

10.00% 10.00%

Publicador:

Resumo:

Acute promyelocytic leukemia (APL) is characterized by the presence of the t(15;17) and PML-RARa rearrangement, with good response to treatment with retinoids. However, few cases of variant APL involving alternative chromosomal aberrations have been reported, including t(11;17)(q23;q21) (Wells et al. in Nat Genet 17:109-113, 1; Arnould et al. in Hum Mol Genet 8:1741-1749, 2) t(5;17)(q35;q12-21), t(11;17)(q13;q21) (Grimwade et al in Blood 96:1297-1308, 3) and der(17) (Rego et al. in Blood (ASH Annual Meeting Abstracts)114:Abstract 6, 4), whereby RARa is fused to the PLZF, NPM, NuMA, and STAT5b genes, respectively, have been described. These cases are characterized by distinct morphology, clinical presentation, and in respect to PLZF, a lack of differentiation response to retinoids leading to the need of different approaches concerning diagnostic methods and therapeutics. This paper describes two cases of APL associated with the PLZF-RARA fusion gene enrolled in the IC-APL trial that is a non-randomized, multicenter study conducted in Brazil, Mexico, Chile and Uruguay with the aim to improve the treatment outcome of APL patients in developing countries. These cases, although rare, offer a challenge to its early recognition and proper conduction.

Relevância:

10.00% 10.00%

Publicador:

Resumo:

The genus Methylobacterium comprises pink-pigmented facultative methylotrophic (PPFM) bacteria, known to be an important plant-associated bacterial group. Species of this group, described as plant-nodulating, have the dual capacity of producing cytokinin and enzymes, such as pectinase and cellulase, involved in systemic resistance induction and nitrogen fixation under specific plant environmental conditions. The aim hereby was to evaluate the phylogenetic distribution of Methylobacterium spp. isolates from different host plants. Thus, a comparative analysis between sequences from structural (16S rRNA) and functional mxaF (which codifies for a subunit of the enzyme methanol dehydrogenase) ubiquitous genes, was undertaken. Notably, some Methylobacterium spp. isolates are generalists through colonizing more than one host plant, whereas others are exclusively found in certain specific plant-species. Congruency between phylogeny and specific host inhabitance was higher in the mxaF gene than in the 16S rRNA, a possible indication of function-based selection in this niche. Therefore, in a first stage, plant colonization by Methylobacterium spp. could represent generalist behavior, possibly related to microbial competition and adaptation to a plant environment. Otherwise, niche-specific colonization is apparently impelled by the host plant.

Relevância:

10.00% 10.00%

Publicador:

Relevância:

10.00% 10.00%

Publicador:

Resumo:

INTRODUZIONE. Presentazione della ricerca e del metedo seguito per realizzarla. CAPITOLO PRIMO. Il contesto storico, politico e sociale di riferimento. - Storia della Siria, - La Siria politica e il conflitto israelo-palestinese - La società siriana: multiculturalismo, tradizione, islam. - Teatro e letteratura in Siria, e nel Bilad AlSham. CAPITOLO SECONDO. I testi. Traduzione integrale di due opere teatrali di Sa’d Allah Wannus. Breve presentazione. - “ Riti di segni e trasformazioni.”, (tukus al-isharat wa-l-tahawwulat), 1994. Il dramma si svolge nella Damasco del XIX secolo, dove un affare di morale e buon costume è il punto di partenza per la metamorfosi dei suoi protagonisti, mettendo a nudo le riflessioni, i desideri più intimi, le contraddizioni e le angosce di una società in crisi. Interessante l’analisi delle figure femminili di questa piece, le loro scelte, il loro ruolo nella società e soprattutto la presa di coscienza delle loro posizioni. - “ I giorni ubriachi.” , (Alayyam Almakhmura), 1997. Il ritratto di una famiglia siriana degli anni trenta. Due genitori, quattro figli, e un nipote che a distanza di anni decide di ripercorrere e raccontarci le loro storie.Una madre che vive tormentata dal suo spettro e che decide di abbandonare la propria famiglia e i propri figli per seguire un altro uomo. Un padre che tiene con violenza le redini delle proprie relazioni, e che rifiuta l’occidente in tutte le sue forme per restare aggrappato alle proprie tradizioni. Un figlio che sceglie l’ordine e la carriera militare, e che, incapace di risolvere il suo rapporto di dipendenza dalla madre, e di risolvere il conflitto tra la legge e un affetto quasi morboso, sceglie di suicidarsi. Un figlio che sceglie la via della perdizione, delle droghe, del furto e degli affari illegali, e che va incontro al successo e alla ricchezza... CAPITOLO TERZO. Biografia di Sa’d Allah Wannus, presentazione delle sue opere principali. Sa’d Allah Wannus (1941 – 1997) è sicuramente uno dei principali protagonisti nell’ambito del teatro arabo contemporaneo. Scrittore, critico, drammaturgo, riformatore, uomo impegnato politicamente, e infine essere umano nella lotta tra la vita e la morte (muore a 56 anni per tumore, dopo un lungo periodo di degenza). Mio intento è quello di analizzare l’opera di quest’autore, attraverso i suoi numerosi scritti e piece teatrali (purtroppo al giorno d’oggi ancora quasi interamente non tradotte dall’arabo), fino ad arrivare, attraverso queste, ad una lettura della società araba contemporanea, e al ruolo che il teatro assume al suo interno. Vita e opere di Sa’ad Allah Wannus. Nasce in Siria nel 1941 in un piccolo villaggio vicino alla città di Tartous, sulla costa mediterranea. Dopo aver terminato gli studi superiori, nel 1959, parte per Il Cairo (Egitto), per studiare giornalismo e letteratura. Rientra a Damasco nel 1964, lavorando al tempo stesso come funzionario al ministero della cultura e come redattore o giornalista in alcune riviste e quotidiani siriani. Nel 1966 parte per Parigi, dove studierà con Jean-Louis Barrault, e dove farà la conoscenza delle tendenze del teatro contemporaneo. Ha l’occasione di incontrare scrittori e critici importanti come Jean Genet e Bernard Dort, nonché di conoscere le teorie sul teatro di Brech e di Piscator, dai quali sarà chiaramente influenzato. In questi anni, e soprattutto in seguito agli avvenimenti del Maggio 1968, si sviluppa in modo determinante la sua coscienza politica, e sono questi gli anni in cui compone alcune tra le sue piece più importanti, come: Serata di gala per il 5 giugno (haflat samar min ajl khamsa huzayran) nel 1968, L’elefante, oh re del tempo! (al-fil, ya malik al-zaman!) 1969, Le avventure della testa del Mamelucco Jaber (Meghamarat ra’s al-mamluk Jabiir) 1970, Una serata con Abu-Khalil al- Qabbani (Sahra ma’a Abi Khalil Al-Qabbani) 1972, Il re è il re (al-malik uwa al-malik) 1977. Parallelamente porta avanti una intensa attività artistica e intellettuale. Soggiorna di nuovo in Francia e a Weimar, per portare a termine la sua formazione teatrale, fonda il Festival di teatro di Damasco, traduce e mette in scena numerosi spettacoli, scrive e pubblica numerosi articoli e una importante serie di studi sul teatro, intitolata: Manifesto per un nuovo teatro arabo (bayanat limasrah ‘arabi jadid) (1970). Scrive in numerose riviste e giornali e fonda la rivista La vita teatrale (al-hayyat al-masrahiyya), del quale sarà capo redattore. La visita del presidente egiziano Anouar Sadat a Gerusalemme nel 1977 e gli accordi di Camp David l’anno seguente, lo gettano in una profonda depressione. E’ l’inizio di un lungo periodo di silenzio e di smarrimento. Ritornerà a scrivere solamente nel 1989, con l’inizio della prima Intifada palestinese, scrive allora una piece teatrale intitolata Lo stupro (al-ightisab), dove presenta un’analisi della struttura dell’elite al potere in Israele. Questo testo apre una nuova epoca creativa, durante la quale Wannus compone alcuni testi molto importanti, nonostante la malattia e il cancro che gli viene diagnosticato nel 1992. Tra questi le pieces Miniature storiche (munamnamat tarakhiyya), nel 1993, e Rituali per una metamorfosi (tukus al-isharat wa-l-tahawwulat), nel 1994 e A proposito della memoria e della morte (‘an al-dhakira wa-l-mawt) nel 1996, una sua ultima opera in cui sono raccolti dei racconti, drammi brevi e una lunga meditazione sulla malattia e la morte. Nel 1997 l’UNESCO gli chiede di redigere il messaggio per la Giornata Mondiale del Teatro, che si tiene ogni anno il 27 marzo. Nel 1997, poche settimane prima della sua scomparsa, realizza insieme ad Omar Almiralay il film documentario Il y a tant de choses a reconter, una intervista in cui Wannus parla della sua opera, e del conflitto Israelo-Palestinese. Muore a 56 anni, il 15 maggio 1997, per un’amara coincidenza proprio il giorno anniversario della creazione di Israele. Wannus drammaturgo engagè: l’importanza del conflitto israelo palestinese nella sua opera. Un’analisi dell’influenza e dell’importanza che le opere di Wannus hanno avuto nel seno della società araba, e soprattutto il suo impegno costante nell’uso del teatro come mezzo per la presa di coscienza del pubblico dei problemi della società contemporanea. Punto cardine dell’opera di Wannus, il conflitto israelo palestinese, e il tentativo costante in alcune sue opere di analizzarne le cause, le strutture, le parti, i giochi di potere. E’ il simbolo di tutta la generazione di Wannus, e delle successive. Analisi delle illusioni e dei miti che la società araba ripropone e che Wannus ha cercato più volte di mettere a nudo. La lotta contro le ipocrisie dei governi, e il tentativo di far prendere coscienza alla società araba del suo ruolo, e delle conseguenze delle sue azioni. L’individuo, la famiglia, la società ... il teatro. Distruggere le apparenze per mettere a nudo l’essere umano nella sua fragilità. CONCLUSIONI. APPENDICE: Intervista con Marie Elias BIBLIOGRAFIA.

Relevância:

10.00% 10.00%

Publicador:

Resumo:

The lack of effective tools have hampered our ability to assess the size, growth and ages of clonal plants. With Serenoa repens (saw palmetto) as a model, we introduce a novel analytical framework that integrates DNA fingerprinting and mathematical modelling to simulate growth and estimate ages of clonal plants. We also demonstrate the application of such life-history information of clonal plants to provide insight into management plans. Serenoa is an ecologically important foundation species in many Southeastern United States ecosystems; yet, many land managers consider Serenoa a troublesome invasive plant. Accordingly, management plans have been developed to reduce or eliminate Serenoa with little understanding of its life history. Using Amplified Fragment Length Polymorphisms, we genotyped 263 Serenoa and 134 Sabal etonia (a sympatric non-clonal palmetto) samples collected from a 20 X 20 m study plot in Florida scrub. Sabal samples were used to assign small field-unidentifiable palmettos to Serenoa or Sabal and also as a negative control for clone detection. We then mathematically modelled clonal networks to estimate genet ages. Our results suggest that Serenoa predominantly propagate via vegetative sprouts and 10000-year-old genets may be common, while showing no evidence of clone formation by Sabal. The results of this and our previous studies suggest that: (i) Serenoa has been part of scrub associations for thousands of years, (ii) Serenoa invasion are unlikely and (ii) once Serenoa is eliminated from local communities, its restoration will be difficult. Reevaluation of the current management tools and plans is an urgent task.

Relevância:

10.00% 10.00%

Publicador:

Resumo:

The lack of effective tools has hampered our ability to assess the size, growth and ages of clonal plants. With Serenoa repens (saw palmetto) as a model, we introduce a novel analytical frame work that integrates DNA fingerprinting and mathematical modelling to simulate growth and estimate ages of clonal plants. We also demonstrate the application of such life-history information of clonal plants to provide insight into management plans. Serenoa is an ecologically important foundation species in many Southeastern United States ecosystems; yet, many land managers consider Serenoa a troublesome invasive plant. Accordingly, management plans have been developed to reduce or eliminate Serenoa with little understanding of its life history. Using Amplified Fragment Length Polymorphisms, we genotyped 263 Serenoa and 134 Sabal etonia (a sympatric non-clonal palmetto) samples collected from a 20 x 20 m study plot in Florida scrub. Sabal samples were used to assign small field-unidentifiable palmettos to Serenoa or Sabal and also as a negative control for clone detection. We then mathematically modelled clonal networks to estimate genet ages. Our results suggest that Serenoa predominantly propagate via vegetative sprouts and 10000-year-old genets maybe common, while showing no evidence of clone formation by Sabal. The results of this and our previous studies suggest that: (i) Serenoa has been part of scrub associations for thousands of years, (ii) Serenoa invasions are unlikely and (ii) once Serenoa is eliminated from local communities, its restoration will be difficult. Reevaluation of the current management tools and plans is an urgent task.