Cloning of genes pal b and pal f of aspergillus nidulans (1995)
- Authors:
- USP affiliated authors: ROSSI FILHO, ANTONIO - FFCLRP ; ROSSI, NILCE MARIA MARTINEZ - FMRP
- Schools: FFCLRP; FMRP
- Subject: GENÉTICA
- Language: Inglês
- Imprenta:
- Place of publication: Pacific Grove
- Date published: 1995
- Source:
- Título do periódico: Abstracts
- Conference title: Fungal Genetics Conference
-
ABNT
MACCHERONI JÚNIOR, W; MARTINEZ-ROSSI, Nilce Maria; MAY, G S; ROSSI, Antônio. Cloning of genes pal b and pal f of aspergillus nidulans. Anais.. Pacific Grove: [s.n.], 1995. -
APA
Maccheroni Júnior, W., Martinez-Rossi, N. M., May, G. S., & Rossi, A. (1995). Cloning of genes pal b and pal f of aspergillus nidulans. In Abstracts. Pacific Grove. -
NLM
Maccheroni Júnior W, Martinez-Rossi NM, May GS, Rossi A. Cloning of genes pal b and pal f of aspergillus nidulans. Abstracts. 1995 ; -
Vancouver
Maccheroni Júnior W, Martinez-Rossi NM, May GS, Rossi A. Cloning of genes pal b and pal f of aspergillus nidulans. Abstracts. 1995 ; - The transcriptional modulators nuc-1 and pacC-1 from N.crassa are required for the expression of a heat shock-inducible gene of the hsp70 family
- Expressão diferencial de genes no dermatófito Trichophyton rubrum em linhagens selvagem e resistente ao ácido undecanóico
- Fosfatase alcalina
- Full virulence of the dermatophyte Trichophyton rubrum is dependent on transcription factor PacC
- Resposta do dermatófito Trichophyton rubrum ao antifúngico Anfotericina B
- Supression subtractive hybridization analyses identified gene up-regulated in the palA1 mutant strain of Aspergillus nidulans
- Effect of culture conditions on the transcription levels of pacC gene in Aspergillus nidulans
- Identificação dos genes do dermatófito Trichophyton rubrum envolvidos no sensoriamento do pH alcalino
- Over-expression of genes coding for proline oxidase, riboflavin kinase, cytochrome C oxidase and an MFS transporter induced by acriflavin in Trichophyton rubrum
- Selection of appropriate housekeeping genes for gene expression studies by qRT-PCR in the dermatophyte Trichophyton rubrum
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