Ramalho AS - Search Results

1

Five percent of normal cystic fibrosis transmembrane conductance regulator mRNA ameliorates the severity of pulmonary disease in cystic fibrosis.

Ramalho AS, Beck S, Meyer M, Penque D, Cutting GR, Amaral MD. Ramalho AS, et al. Am J Respir Cell Mol Biol. 2002 Nov;27(5):619-27. doi: 10.1165/rcmb.2001-0004OC. Am J Respir Cell Mol Biol. 2002. PMID: 12397022

2

Transcript analysis of the cystic fibrosis splicing mutation 1525-1G>A shows use of multiple alternative splicing sites and suggests a putative role of exonic splicing enhancers.

Ramalho AS, Beck S, Penque D, Gonska T, Seydewitz HH, Mall M, Amaral MD. Ramalho AS, et al. J Med Genet. 2003 Jul;40(7):e88. doi: 10.1136/jmg.40.7.e88. J Med Genet. 2003. PMID: 12843337 Free PMC article. No abstract available.

3

Methods for RNA extraction, cDNA preparation and analysis of CFTR transcripts.

Ramalho AS, Beck S, Farinha CM, Clarke LA, Heda GD, Steiner B, Sanz J, Gallati S, Amaral MD, Harris A, Tzetis M. Ramalho AS, et al. J Cyst Fibros. 2004 Aug;3 Suppl 2:11-5. doi: 10.1016/j.jcf.2004.05.004. J Cyst Fibros. 2004. PMID: 15463918 Free article. Review.

4

Quantitative methods for the analysis of CFTR transcripts/splicing variants.

Amaral MD, Clarke LA, Ramalho AS, Beck S, Broackes-Carter F, Rowntree R, Mouchel N, Williams SH, Harris A, Tzetis M, Steiner B, Sanz J, Gallati S, Nissim-Rafinifa M, Kerem B, Hefferon T, Cutting GR, Goina E, Pagani F. Amaral MD, et al. Among authors: ramalho as. J Cyst Fibros. 2004 Aug;3 Suppl 2:17-23. doi: 10.1016/j.jcf.2004.05.047. J Cyst Fibros. 2004. PMID: 15463919 Free article. Review.

5

CFTR Cl- channel function in native human colon correlates with the genotype and phenotype in cystic fibrosis.

Hirtz S, Gonska T, Seydewitz HH, Thomas J, Greiner P, Kuehr J, Brandis M, Eichler I, Rocha H, Lopes AI, Barreto C, Ramalho A, Amaral MD, Kunzelmann K, Mall M. Hirtz S, et al. Gastroenterology. 2004 Oct;127(4):1085-95. doi: 10.1053/j.gastro.2004.07.006. Gastroenterology. 2004. PMID: 15480987

6

Bacterial transfer of large functional genomic DNA into human cells.

Laner A, Goussard S, Ramalho AS, Schwarz T, Amaral MD, Courvalin P, Schindelhauer D, Grillot-Courvalin C. Laner A, et al. Among authors: ramalho as. Gene Ther. 2005 Nov;12(21):1559-72. doi: 10.1038/sj.gt.3302576. Gene Ther. 2005. PMID: 15973438

7

Characterization of novel airway submucosal gland cell models for cystic fibrosis studies.

da Paula AC, Ramalho AS, Farinha CM, Cheung J, Maurisse R, Gruenert DC, Ousingsawat J, Kunzelmann K, Amaral MD. da Paula AC, et al. Among authors: ramalho as. Cell Physiol Biochem. 2005;15(6):251-62. doi: 10.1159/000087235. Cell Physiol Biochem. 2005. PMID: 16037690 Free article.

8

Deletion of CFTR translation start site reveals functional isoforms of the protein in CF patients.

Ramalho AS, Lewandowska MA, Farinha CM, Mendes F, Gonçalves J, Barreto C, Harris A, Amaral MD. Ramalho AS, et al. Cell Physiol Biochem. 2009;24(5-6):335-46. doi: 10.1159/000257426. Epub 2009 Nov 4. Cell Physiol Biochem. 2009. PMID: 19910674 Free PMC article.

9

Escherichia coli-cloned CFTR loci relevant for human artificial chromosome therapy.

Rocchi L, Braz C, Cattani S, Ramalho A, Christan S, Edlinger M, Ascenzioni F, Laner A, Kraner S, Amaral M, Schindelhauer D. Rocchi L, et al. Hum Gene Ther. 2010 Sep;21(9):1077-92. doi: 10.1089/hum.2009.225. Hum Gene Ther. 2010. PMID: 20384480

10

Quantification of CFTR transcripts.

Ramalho AS, Clarke LA, Amaral MD. Ramalho AS, et al. Methods Mol Biol. 2011;741:115-35. doi: 10.1007/978-1-61779-117-8_9. Methods Mol Biol. 2011. PMID: 21594782

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