Human semaphorin 6B [(HSA)SEMA6B], a novel human class 6 semaphorin gene: alternative splicing and all-trans-retinoic acid-dependent downregulation in glioblastoma cell lines (2001)
- Authors:
- USP affiliated authors: BRENTANI, MARIA MITZI - FM ; SOGAYAR, MARI CLEIDE - IQ
- Unidades: FM; IQ
- Subjects: BIOQUÍMICA; GENES
- Language: Inglês
- Imprenta:
- Source:
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ABNT
CORREA, R. G. et al. Human semaphorin 6B [(HSA)SEMA6B], a novel human class 6 semaphorin gene: alternative splicing and all-trans-retinoic acid-dependent downregulation in glioblastoma cell lines. Genomics, v. 73, n. 3, p. 343-348, 2001Tradução . . Disponível em: http://www.idealibrary.com/links/doi/10.1006/geno.2001.6525/pdf. Acesso em: 26 fev. 2026. -
APA
Correa, R. G., Sasahara, R. M., Bengtson, M. H., Katayama, M. L. H., Salim, A. C. M., Brentani, M. M., et al. (2001). Human semaphorin 6B [(HSA)SEMA6B], a novel human class 6 semaphorin gene: alternative splicing and all-trans-retinoic acid-dependent downregulation in glioblastoma cell lines. Genomics, 73( 3), 343-348. Recuperado de http://www.idealibrary.com/links/doi/10.1006/geno.2001.6525/pdf -
NLM
Correa RG, Sasahara RM, Bengtson MH, Katayama MLH, Salim ACM, Brentani MM, Sogayar MC, Souza SJ, Simpson AJG. Human semaphorin 6B [(HSA)SEMA6B], a novel human class 6 semaphorin gene: alternative splicing and all-trans-retinoic acid-dependent downregulation in glioblastoma cell lines [Internet]. Genomics. 2001 ; 73( 3): 343-348.[citado 2026 fev. 26 ] Available from: http://www.idealibrary.com/links/doi/10.1006/geno.2001.6525/pdf -
Vancouver
Correa RG, Sasahara RM, Bengtson MH, Katayama MLH, Salim ACM, Brentani MM, Sogayar MC, Souza SJ, Simpson AJG. Human semaphorin 6B [(HSA)SEMA6B], a novel human class 6 semaphorin gene: alternative splicing and all-trans-retinoic acid-dependent downregulation in glioblastoma cell lines [Internet]. Genomics. 2001 ; 73( 3): 343-348.[citado 2026 fev. 26 ] Available from: http://www.idealibrary.com/links/doi/10.1006/geno.2001.6525/pdf - Claudin 4 and 7 Expression Is Not Correlated to Triple Negative Phenotype in Invasive NOS Breast Carcinomas: A Wide Series Assessed by Immunohistochemistry
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