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1.
J Mycol Med ; 27(2): 250-253, 2017 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-28391957

RESUMEN

INTRODUCTION: Dermatophytic disease individualized by Hadida and Schousboe in 1959 is a rare form of chronic dermatophyte infection; characterized by subcutaneous and visceral invasion and a therapeutic failure. We report a case of dermatophytic disease with brain abscess in an Algerian patient. OBSERVATIONS: The patient was 47-year-old, she was born parents first cousins. She had since the age of 10 years scaly scalp lesions that became secondarily papular and nodular. At the age of 17 years, the patient had a generalized skin involvement with multiple nodular lesions, diffuse disease of the nails (plurionyxis), poly lymphadenopathies affecting the cervical, axillary and inguinal areas. Mycological tests identified Trichophyton rubrum. Histopathological examinations showed caseiform necrosis with epithelioid and giant cells. PAS staining showed hyphae in necrosis. The rest of the blood and urine tests were normal. Sequencing CARD9 allowed to highlight a homozygous mutation Q289X. The evolution was marked by an appearance at the age of 47 of a right cerebral abscess fronto-temporo-parietal, cortico-subcortical detected by MRI. The patient was given itraconazole 200mg/day with good evolution after three months of decline. DISCUSSION: Dermatophytic disease is very rare. Fifty cases have been published, mostly from North Africa, a strong endogamy region. Signs and symptoms almost always start with a scalp ringworm with almost constant occurrence of complications: in our patient a cerebral localization with a good evolution with itraconazole. Immunologically it is characterized by an autosomal recessive deficiency CARD9. This observation is notable for the onset of the disease at an early age, the dermatophyte T. rubrum and the favourable outcome of the brain lesion with itraconazole. CONCLUSION: Dermatophytic disease is rare, often severe. Our case is original because of the occurrence of a cerebral localization with good response to itraconazole and its mechanism of action deserves to be elucidated.


Asunto(s)
Proteínas Adaptadoras de Señalización CARD/genética , Infecciones Fúngicas del Sistema Nervioso Central/diagnóstico , Tiña/diagnóstico , Argelia , Infecciones Fúngicas del Sistema Nervioso Central/tratamiento farmacológico , Infecciones Fúngicas del Sistema Nervioso Central/genética , Consanguinidad , Dermatomicosis/complicaciones , Dermatomicosis/diagnóstico , Dermatomicosis/tratamiento farmacológico , Dermatomicosis/genética , Femenino , Homocigoto , Humanos , Itraconazol/uso terapéutico , Persona de Mediana Edad , Mutación Missense , Tiña/tratamiento farmacológico , Tiña/genética , Trichophyton
2.
Sci Total Environ ; 500-501: 211-23, 2014 Dec 01.
Artículo en Inglés | MEDLINE | ID: mdl-25217996

RESUMEN

Groundwater pollution from anthropogenic sources is a serious concern affecting several coastal aquifers worldwide. Increasing groundwater exploitation, coupled with point and non-point pollution sources, are the main anthropogenic impacts on coastal environments and are responsible for severe health and food security issues. Adequate management strategies to protect groundwater from contamination and overexploitation are of paramount importance, especially in arid prone regions, where coastal aquifers often represent the main freshwater resource to sustain human needs. The Bou-Areg Aquifer (Morocco) is a perfect example of a coastal aquifer constantly exposed to all the negative externalities associated with groundwater use for agricultural purposes, which lead to a general increase in aquifer salinization. In this study data on 61 water samples, collected in June and November 2010, were used to: (i) track groundwater composition changes related to the use of irrigation water from different sources, (ii) highlight seasonal variations to assess aquifer vulnerability, and (iii) present a reproducible example of multi-tracer approach for groundwater management in rural coastal areas. Hydrogeochemical results show that Bou-Areg groundwater is characterized by - high salinity, associated with a remarkable increase in bicarbonate content in the crop growing season, due to more intense biological activity in irrigated soils. The coupled multi-tracer and statistical analysis confirms the strong dependency on irrigation activities as well as a clear identification of the processes governing the aquifer's hydrochemistry in the different seasons. Water Rock Interaction (WRI) dominates the composition of most of groundwater samples in the Low Irrigation season (L-IR) and Agricultural Return Flow (ARF) mainly affects groundwater salinization in the High Irrigation season (H-IR) in the same areas naturally affected by WRI. In the central part of the plain River Recharge (RR) from the Selouane River is responsible for the high groundwater salinity whilst Mixing Processes (MIX) occur in absence of irrigation activities.


Asunto(s)
Monitoreo del Ambiente/métodos , Agua Subterránea/química , Contaminantes Químicos del Agua/análisis , Contaminación Química del Agua/estadística & datos numéricos , Recursos Hídricos/estadística & datos numéricos , Abastecimiento de Agua/estadística & datos numéricos , Agricultura , Agua Subterránea/análisis , Humanos , Marruecos , Movimientos del Agua , Recursos Hídricos/análisis , Abastecimiento de Agua/análisis
3.
Artículo en Francés | MEDLINE | ID: mdl-23838247

RESUMEN

INTRODUCTION: Cowden syndrome is rare; oral symptoms are not always diagnosed. This case of Cowden syndrome was revealed by gingival hypertrophy. OBSERVATION: A 21-year-old female patient consulted for gingival hypertrophy and multiple papules in the mouth. She had a history of thyroid lobectomy due to a goiter. The gingival papillomatosis and the goiter suggested a Cowden syndrome. The diagnosis was confirmed clinically by facial skin papules. DISCUSSION: Cutaneous and oral lesions are usually the first symptoms of the syndrome. Diffuse gingival papillomatosis may suggest a Cowden syndrome and should lead to screen for associated symptoms. A high-risk diagnosis of breast and thyroid cancer is associated to Cowden syndrome and the patient should have a yearly follow-up.


Asunto(s)
Hipertrofia Gingival/diagnóstico , Síndrome de Hamartoma Múltiple/diagnóstico , Ciego , Femenino , Hipertrofia Gingival/etiología , Síndrome de Hamartoma Múltiple/complicaciones , Humanos , Pólipos Intestinales/diagnóstico , Pólipos Intestinales/etiología , Adulto Joven
7.
Gastroenterol Clin Biol ; 33(2): 115-7, 2009 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-19201118

RESUMEN

Ophthalmological complications with interferon therapy are rare, usually mild and reversible, and do not require the withdrawal of antiviral treatment. Anterior ischemic optic neuropathy is an uncommon complication of interferon treatment. From January 1998 to December 2007, three patients developed anterior ischemic optic neuropathy during antiviral treatment, with a favourable course after interferon was discontinued. Periodic Ophthalmological examinations, including visual acuity and fundus examinations should be performed before starting and during treatment, particularly in patients with vascular risk factors. Antiviral therapy should be stopped immediately if severe ophthalmologic complications occur.


Asunto(s)
Antivirales/efectos adversos , Hepatitis C Crónica/tratamiento farmacológico , Interferón-alfa/efectos adversos , Neuropatía Óptica Isquémica/inducido químicamente , Ribavirina/efectos adversos , Anciano , Antivirales/uso terapéutico , Femenino , Angiografía con Fluoresceína , Fondo de Ojo , Humanos , Interferón alfa-2 , Interferón-alfa/uso terapéutico , Masculino , Persona de Mediana Edad , Neuropatía Óptica Isquémica/diagnóstico , Neuropatía Óptica Isquémica/terapia , Papiledema/diagnóstico , Proteínas Recombinantes , Ribavirina/uso terapéutico , Agudeza Visual
11.
Digestion ; 74(2): 69-77, 2006.
Artículo en Inglés | MEDLINE | ID: mdl-17135728

RESUMEN

BACKGROUND/AIMS: Sedation rates may vary among countries, depending on patients' and endoscopists' preferences. The aim of this survey was to investigate the rate of using premedication for routine diagnostic upper gastrointestinal (UGI) endoscopy in endoscopy societies, members of the European Society of Gastrointestinal Endoscopy (ESGE). METHODS: We evaluated a multiple-choice questionnaire which was e-mailed to representatives of national endoscopy societies, which are members of the ESGE. The questionnaire had 14 items referring to endoscopy practices in each country and the representatives' endoscopy units. RESULTS: The response rate was 76% (34/45). In 47% of the countries, less than 25% of patients undergo routine diagnostic UGI endoscopy with conscious sedation. In 62% of the responders' endoscopy units, patients are not asked their preference for sedation and do not sign a consent form (59%). Common sedatives in use are midazolam (82%), diazepam (38%) or propofol (47%). Monitoring equipment is not available 'in most of the endoscopy units' in 46% (13/28) of the countries. Though they were available in 91% of the national representatives' endoscopy units, they are rarely (21%) used to monitor unsedated routine diagnostic UGI endoscopy. CONCLUSIONS: In about 50% of ESGE-related countries, less than 25% of patients are sedated for routine diagnostic UGI endoscopy. Major issues to improve include availability of monitoring equipment and the use of a consent form.


Asunto(s)
Sedación Consciente/estadística & datos numéricos , Endoscopía Gastrointestinal , Enfermedades Gastrointestinales/diagnóstico , Femenino , Encuestas de Atención de la Salud , Humanos , Hipnóticos y Sedantes/administración & dosificación , Masculino , Sociedades Médicas , Encuestas y Cuestionarios
12.
Biochem Soc Trans ; 34(Pt 1): 39-42, 2006 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-16246174

RESUMEN

NMD (nonsense-mediated mRNA decay) is a cellular quality-control mechanism in which an otherwise stable mRNA is destabilized by the presence of a premature termination codon. We have defined the set of endogenous NMD substrates, demonstrated that they are available for NMD at every round of translation, and showed that premature termination and normal termination are not equivalent biochemical events. Premature termination is aberrant, and its NMD-stimulating defects can be reversed by the presence of tethered poly(A)-binding protein (Pab1p) or tethered eRF3 (eukaryotic release factor 3) (Sup35p). Thus NMD appears to be triggered by a ribosome's failure to terminate adjacent to a properly configured 3'-UTR (untranslated region), an event that may promote binding of the UPF/NMD factors to stimulate mRNA decapping.


Asunto(s)
Regiones no Traducidas 3' , Codón sin Sentido , Biosíntesis de Proteínas , ARN Mensajero/metabolismo , Factores de Terminación de Péptidos , Proteína I de Unión a Poli(A)/metabolismo , Priones/metabolismo , Proteínas de Saccharomyces cerevisiae/metabolismo
13.
Mol Cell Biol ; 18(12): 7383-96, 1998 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-9819425

RESUMEN

The poly(A) tail of an mRNA is believed to influence the initiation of translation, and the rate at which the poly(A) tail is removed is thought to determine how fast an mRNA is degraded. One key factor associated with this 3'-end structure is the poly(A)-binding protein (Pab1p) encoded by the PAB1 gene in Saccharomyces cerevisiae. In an effort to learn more about the functional role of this protein, we used a two-hybrid screen to determine the factor(s) with which it interacts. We identified five genes encoding factors that specifically interact with the carboxy terminus of Pab1p. Of a total of 44 specific clones identified, PBP1 (for Pab1p-binding protein) was isolated 38 times. Of the putative interacting genes examined, PBP1 promoted the highest level of resistance to 3-aminotriazole (>100 mM) in constructs in which HIS3 was used as a reporter. We determined that a fraction of Pbp1p cosediments with polysomes in sucrose gradients and that its distribution is very similar to that of Pab1p. Disruption of PBP1 showed that it is not essential for viability but can suppress the lethality associated with a PAB1 deletion. The suppression of pab1Delta by pbp1Delta appears to be different from that mediated by other pab1 suppressors, since disruption of PBP1 does not alter translation rates, affect accumulation of ribosomal subunits, change mRNA poly(A) tail lengths, or result in a defect in mRNA decay. Rather, Pbp1p appears to function in the nucleus to promote proper polyadenylation. In the absence of Pbp1p, 3' termini of pre-mRNAs are properly cleaved but lack full-length poly(A) tails. These effects suggest that Pbp1p may act to repress the ability of Pab1p to negatively regulate polyadenylation.


Asunto(s)
Proteínas Portadoras/genética , Regulación Fúngica de la Expresión Génica/genética , Genes Fúngicos/genética , Poli A/genética , Proteínas de Unión al ARN/genética , Proteínas de Saccharomyces cerevisiae , Saccharomyces cerevisiae/genética , Secuencia de Aminoácidos , Clonación Molecular , Proteínas Fúngicas/genética , Eliminación de Gen , Genes Reporteros , Datos de Secuencia Molecular , Proteínas Nucleares/genética , Oligonucleótidos/genética , Proteínas de Unión a Poli(A) , Polirribosomas/genética , Biosíntesis de Proteínas/genética , ARN Mensajero/genética , Proteínas de Unión al ARN/química , Alineación de Secuencia , Análisis de Secuencia de ADN
14.
Mol Cell Biol ; 17(7): 3694-701, 1997 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-9199303

RESUMEN

In Saccharomyces cerevisiae, the single poly(A) binding protein, Pab1, is the major ribonucleoprotein associated with the poly(A) tails of mRNAs in both the nucleus and the cytoplasm. We found that Pab1 interacts with Rna15 in two-hybrid assays and in coimmunoprecipitation experiments. Overexpression of PAB1 partially but specifically suppressed the rna15-2 mutation in vivo. RNA15 codes for a component of the cleavage and polyadenylation factor CF I, one of the four factors needed for pre-mRNA 3'-end processing. We show that Pab1 and CF I copurify in anion-exchange chromatography. These data suggest that Pab1 is physically associated with CF I. Extracts from a thermosensitive pab1 mutant and from a wild-type strain immunoneutralized for Pab1 showed normal cleavage activity but a large increase in poly(A) tail length. A normal tail length was restored by adding recombinant Pab1 to the mutant extract. The longer poly(A) tails were not due to an inhibition of exonuclease activities. Pab1 has previously been implicated in the regulation of translation initiation and in cytoplasmic mRNA stability. Our data indicate that Pab1 is also a part of the 3'-end RNA-processing complex and thus participates in the control of the poly(A) tail lengths during the polyadenylation reaction.


Asunto(s)
Proteínas Fúngicas/fisiología , Regulación Fúngica de la Expresión Génica , Proteínas Nucleares/fisiología , Poli A/metabolismo , ARN Mensajero/metabolismo , Proteínas de Unión al ARN/fisiología , Proteínas de Saccharomyces cerevisiae , Saccharomyces cerevisiae/genética , Factores de Escisión y Poliadenilación de ARNm , Exorribonucleasas/metabolismo , Prueba de Complementación Genética , Proteínas de Unión a Poli(A) , Unión Proteica , Biosíntesis de Proteínas
15.
J Clin Endocrinol Metab ; 82(4): 1261-73, 1997 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-9100605

RESUMEN

The rule of Ramadan (1 month of food and water intakes restricted to night hours) is followed by the majority of the Moslem fraction of the human population, but the possible consequences of this long-lasting modification of food intake schedule on public health have not yet been extensively documented. Therefore, a group of healthy control subjects and a group of healed duodenal ulcer patients were studied before (controls), during (both groups), and after (both groups) the month of Ramadan. The time-restricted food and water intakes were associated with variations of gastric pH, plasma gastrin, insulin, glucose, and calcium documented on a circadian basis. All of the studied biological variables, except insulin, underwent changes in their 24-h mean concentration (e.g. decrease in gastric pH, increase in plasma gastrin), some of which were still present 1 month after the end of Ramadan. The circadian patterns of all the studied variables were altered during the month of Ramadan. Some differences between the group of healthy control subjects and the group of healed duodenal ulcer patients may suggest a greater susceptibility of the latter to the modifications of feeding and sleeping schedule, which could possibly be a risk factor for the disease.


Asunto(s)
Ritmo Circadiano , Dieta , Ayuno , Islamismo , Adulto , Glucemia/análisis , Calcio/sangre , Úlcera Duodenal/metabolismo , Mucosa Gástrica/metabolismo , Gastrinas/sangre , Humanos , Concentración de Iones de Hidrógeno , Masculino , Valores de Referencia , Cicatrización de Heridas
16.
Mol Cell Biol ; 17(3): 1102-9, 1997 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-9032237

RESUMEN

Cleavage and polyadenylation factor I (CF I) is one of four factors required in vitro for yeast pre-mRNA 3'-end processing. Two protein components of this factor, encoded by genes RNA14 and RNA15, have already been identified. We describe here another gene, PCF11 (for protein 1 of CF I), that genetically interacts with RNA14 and RNA15 and which presumably codes for a third protein component of CF I. This gene was isolated in a two-hybrid screening designed to identify proteins interacting with Rna14 and Rna15. PCF11 is an essential gene encoding for a protein of 626 amino acids having an apparent molecular mass of 70 kDa. Thermosensitive mutations in PCF11 are synergistically lethal with thermosensitive alleles of RNA14 and RNA15. The Pcf11-2 thermosensitive strain shows a shortening of the poly(A) tails and a strong decrease in the steady-state level of actin transcripts after a shift to the nonpermissive temperature as do the thermosensitive alleles of RNA14 and RNA15. Extracts from the pcf11-1 and pcf11-2 thermosensitive strains and the wild-type strain, when Pcf11 is neutralized by specific antibodies, are deficient in cleavage and polyadenylation. Moreover, fractions obtained by anion-exchange chromatography of extracts from the wild-type strain contain both Pcf11 and Rna15 in the same fractions, as shown by immunoblotting with a Pcf11-specific antibody.


Asunto(s)
Citocromos c , Procesamiento Postranscripcional del ARN/genética , ARN de Hongos/metabolismo , ARN Mensajero/metabolismo , Proteínas de Saccharomyces cerevisiae , Levaduras/genética , Secuencia de Aminoácidos , Grupo Citocromo c/genética , Proteínas Fúngicas/genética , Genes Fúngicos/genética , Genes Letales , Datos de Secuencia Molecular , Mutación , Proteínas Nucleares/genética , Proteínas de Unión al ARN/genética , Proteínas de Unión al ARN/aislamiento & purificación , Factores de Escisión y Poliadenilación de ARNm
17.
Bull Cancer ; 84(2): 218-22, 1997 Feb.
Artículo en Francés | MEDLINE | ID: mdl-9180849

RESUMEN

We report here 2 cases of breast angiosarcoma observed at Centre Val-d' Aurelle of Montpellier over a period of 14 years (1980 to 1994). Based on a review of literature, we analyze the epidemiological, pathological, clinical, diagnostic and treatment aspects of this rare type of breast cancer. The difficulties of histological diagnosis are underlined. Mastectomy is the treatment of reference. Breast angiosarcoma has the worst prognosis of all mammary malignancies, with a mean survival of 24 months. The low histologic grade and an early diagnosis are the most important factors of good prognosis. The benefit of irradiation and chemotherapy as adjuvant therapy remains to be demonstrated.


Asunto(s)
Neoplasias de la Mama/terapia , Hemangiosarcoma/terapia , Mastectomía , Anciano , Protocolos de Quimioterapia Combinada Antineoplásica/uso terapéutico , Neoplasias de la Mama/mortalidad , Neoplasias de la Mama/patología , Quimioterapia Adyuvante , Terapia Combinada , Resultado Fatal , Femenino , Hemangiosarcoma/mortalidad , Hemangiosarcoma/patología , Humanos , Escisión del Ganglio Linfático , Persona de Mediana Edad , Metástasis de la Neoplasia , Estadificación de Neoplasias , Pronóstico , Dosificación Radioterapéutica
18.
Gastroenterol Clin Biol ; 21(11): 813-9, 1997.
Artículo en Francés | MEDLINE | ID: mdl-9587531

RESUMEN

OBJECTIVES: Lifestyle changes during Ramadan as the meals are taken exclusively in the evening, and nightly sleep is often delayed and shortened. The wake/sleep cycle is also modified. The aim of this study was to evaluate the influence of Ramadan on gastric acidity in healthy volunteers. METHODS: Nine healthy volunteers had 24-hour measurement of the gastric pH; 4 periods were compared: one week prior to Ramadan, day 10 and day 24 during Ramadan, and one month after Ramadan. The pH profiles and the [H+] activity (area under the curve) were measured during 24 hours, the night phase (5PM-8AM) and diurnal phase (8AM-5PM). RESULTS: The diurnal variations of the pH profile were more significant; the median pH was 2.3 prior to Ramadan, 1 at day 10 and day 24 and 1.6 one month after Ramadan. The 24-hours [H+] activity increased by 45% at day 10 of Ramadan compared with its level prior to Ramadan. This increase was mostly diurnal (+122%) and also nightly (+25%). The activity [H+] was steady during Ramadan. One month after Ramadan, the 24-hours [H+] activity was 23% higher than the one noted before Ramadan. CONCLUSIONS: This study shows that the conditions of feeding imposed by Ramadan are associated with an increase of the gastric acidity mainly in diurnal phase. These results do not explain the origin of the healthy volunteer digestive symptoms encountered during Ramadan.


Asunto(s)
Ayuno , Ácido Gástrico/metabolismo , Islamismo , Adulto , Glucemia/análisis , Calcio/sangre , Ritmo Circadiano , Determinación de la Acidez Gástrica , Gastrinas/sangre , Humanos , Concentración de Iones de Hidrógeno , Insulina/sangre , Masculino , Religión y Medicina , Factores de Tiempo
19.
Bull Cancer ; 84(9): 881-4, 1997 Sep.
Artículo en Francés | MEDLINE | ID: mdl-9435810

RESUMEN

Based upon the literature, we discuss epidemiological, histopathological, clinical and treatment aspects of postirradiation sarcomas. The risk of postirradiation sarcoma is very low and negligible in comparison with the beneficial effect of radiotherapy, and it should not be a major factor influencing treatment decision in patients with cancer. The radical surgical approach of postirradiation sarcoma is the treatment which offers the best chance for cure.


Asunto(s)
Neoplasias Inducidas por Radiación , Sarcoma , Humanos , Neoplasias Inducidas por Radiación/diagnóstico , Neoplasias Inducidas por Radiación/mortalidad , Neoplasias Inducidas por Radiación/radioterapia , Neoplasias Inducidas por Radiación/cirugía , Pronóstico , Radioterapia/efectos adversos , Dosificación Radioterapéutica , Factores de Riesgo , Sarcoma/diagnóstico , Sarcoma/mortalidad , Sarcoma/radioterapia , Sarcoma/cirugía , Análisis de Supervivencia
20.
Mol Gen Genet ; 252(5): 552-62, 1996 Oct 16.
Artículo en Inglés | MEDLINE | ID: mdl-8914516

RESUMEN

In a search for proteins associated with Rna15p in processing the 3' ends of messenger RNAs, we have looked for suppressors that correct, even partially, the thermosensitive growth defect of the rna15-2 mutant. Mutations in a single locus that we named SSM5, were able to suppress both the thermosensitivity of cell growth and the mRNA 3' processing defect associated with the rna15-2 mutation, but only slightly alleviated the thermosensitive growth defect of an rna14-1 mutant. The ssm5-1 mutant is sensitive to hydroxyurea at 37 degrees C, a drug that inhibits DNA synthesis. By screening for complementation of the hydroxyurea-sensitive phenotype we cloned the corresponding wild-type gene and found that it corresponds to the essential gene STS1 (also named DBF8). Sts1p has an apparent molecular weight of 30 kDa and was confirmed to be a cytosolic protein by immunofluorescence analysis. Western blot analysis indicates that the thermosensitive mutant strains rna15-2, rna14-1 and pap1-1 present a very low level of the Rna15p at 37 degrees C. The ssm5-1 mutation restores the level of Rna15p in the rna15-2 ssm5-1 double mutant. Use of the two-hybrid system suggests that Sts1p does not interact directly with Rna15p, but may be active as a homodimer. The present data suggest that Sts1p may play a role in the transport of Rna15p from the cytoplasm to the nucleus.


Asunto(s)
Transportadoras de Casetes de Unión a ATP/genética , Sistemas de Transporte de Aminoácidos , Proteínas Fúngicas/genética , Mutación , Proteínas Nucleares/genética , Polinucleotido Adenililtransferasa , Procesamiento Postranscripcional del ARN , Proteínas de Saccharomyces cerevisiae , Saccharomyces cerevisiae/genética , Factores de Escisión y Poliadenilación de ARNm , Transportadoras de Casetes de Unión a ATP/química , Transportadoras de Casetes de Unión a ATP/metabolismo , Alelos , Secuencia de Bases , Proteínas Fúngicas/química , Proteínas Fúngicas/metabolismo , Regulación Fúngica de la Expresión Génica , Genes Supresores , Prueba de Complementación Genética , Proteínas de la Membrana/genética , Datos de Secuencia Molecular , Proteínas Nucleares/metabolismo , Proteínas Asociadas a Pancreatitis , Poli A/genética , Poli A/metabolismo , ARN Mensajero , Saccharomyces cerevisiae/fisiología , Selección Genética , Fracciones Subcelulares , Temperatura
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