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Results of search for 'au:"Chillon, M"', page 1 of 5
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Authors
Alaejos, I
Alcoceba, M
Alcoceba, Miguel
Balanzategui, A
Balanzategui, Ana
Bosch, A
Casals, T
Chillon, M
Chillón, M
Chillón, M C
Chillón, M Carmen
Estivill, X
García-Sanz, R
García-Sanz, Ramón
Giménez, J
González, M
Mateos, M V
Nunes, V
San Miguel, J F
Sarasquete, M E
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Topics
Adolescent
Adult
Aged
Animals
Base Sequence
Cystic Fibrosis
Cystic Fibrosis Transmembrane Conductance Regulator
Exons
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Humans
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Membrane Proteins
Middle Aged
Molecular Sequence Data
Multiple Myeloma
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Polymerase Chain Reaction
genetics
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g d
Spanish
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1.
Trafficking and propagation of canine adenovirus vectors lacking a known integrin-interacting motif.
[electronic resource]
by
Chillon, M
Kremer, E J
Producer:
20011204
In:
Human gene therapy
vol. 12
Online resources:
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2.
SSCP-polymorphism in intron 12 of the CFTR gene recognized by BcII.
[electronic resource]
by
Chillón, M
Nunes, V
Estivill, X
Producer:
19911231
In:
Nucleic acids research
vol. 19
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3.
Gutless adenovirus: last-generation adenovirus for gene therapy.
[electronic resource]
by
Alba, R
Bosch, A
Chillon, M
Producer:
20060209
In:
Gene therapy
vol. 12 Suppl 1
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4.
A rare DNA variant in exon 15 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.
[electronic resource]
by
Chillón, M
Palacio, A
Nunes, V
Estivill, X
Producer:
19930218
In:
Human genetics
vol. 90
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5.
AAVrh.10 immunogenicity in mice and humans. Relevance of antibody cross-reactivity in human gene therapy.
[electronic resource]
by
Thwaite, R
Pagès, G
Chillón, M
Bosch, A
Producer:
20150930
In:
Gene therapy
vol. 22
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6.
Canine adenovirus vectors: an alternative for adenovirus-mediated gene transfer.
[electronic resource]
by
Kremer, E J
Boutin, S
Chillon, M
Danos, O
Producer:
20000110
In:
Journal of virology
vol. 74
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7.
Identification of a 31-bp insertion (3860ins31) in exon 20 of the cystic fibrosis (CFTR) gene.
[electronic resource]
by
Chillón, M
Casals, T
Nunes, V
Giménez, J
Estivill, X
Producer:
19931105
In:
Human molecular genetics
vol. 2
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8.
Adenovirus complexed with polyethylene glycol and cationic lipid is shielded from neutralizing antibodies in vitro.
[electronic resource]
by
Chillón, M
Lee, J H
Fasbender, A
Welsh, M J
Producer:
19981130
In:
Gene therapy
vol. 5
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9.
PCR detection of the pKM.19/ScrfI RFLP (D7S23), a marker closely linked to the cystic fibrosis mutation.
[electronic resource]
by
Nunes, V
Chillón, M
Lench, N
Ramsay, M
Estivill, X
Producer:
19901011
In:
Nucleic acids research
vol. 18
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10.
Analysis of the CFTR gene in the Spanish population: SSCP-screening for 60 known mutations and identification of four new mutations (Q30X, A120T, 1812-1 G-->A, and 3667del4).
[electronic resource]
by
Chillón, M
Casals, T
Giménez, J
Nunes, V
Estivill, X
Producer:
19940804
In:
Human mutation
vol. 3
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11.
A cystic fibrosis patient homozygous for the new frameshift mutation 936delTA: description and clinical data.
[electronic resource]
by
Chillón, M
Casals, T
Giménez, J
Nunes, V
Estivill, X
Producer:
19940922
In:
Journal of medical genetics
vol. 31
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12.
Secreted αKlotho isoform protects against age-dependent memory deficits.
[electronic resource]
by
Massó, A
Sánchez, A
Bosch, A
Giménez-Llort, L
Chillón, M
Producer:
20190731
In:
Molecular psychiatry
vol. 23
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13.
Identification of a frameshift mutation (1609delCA) in exon 10 of the CFTR gene in seven Spanish cystic fibrosis patients.
[electronic resource]
by
Chillón, M
Palacio, A
Nunes, V
Casals, T
Giménez, J
Estivill, X
Producer:
19930528
In:
Human mutation
vol. 1
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14.
A new missense mutation (E92K) in the first transmembrane domain of the CFTR gene causes a benign cystic fibrosis phenotype.
[electronic resource]
by
Nunes, V
Chillón, M
Dörk, T
Tümmler, B
Casals, T
Estivill, X
Producer:
19930615
In:
Human molecular genetics
vol. 2
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15.
Identification of a new missense mutation (P205S) in the first transmembrane domain of the CFTR gene associated with a mild cystic fibrosis phenotype.
[electronic resource]
by
Chillón, M
Casals, T
Nunes, V
Giménez, J
Pérez Ruiz, E
Estivill, X
Producer:
19940203
In:
Human molecular genetics
vol. 2
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16.
Acceptor splice site mutation in the invariant AG of intron 5 of the protein C gene, causing type I protein C deficiency.
[electronic resource]
by
Soria, J M
Fontcuberta, J
Chillón, M
Borrell, M
Estivill, X
Sala, N
Producer:
19940105
In:
Human genetics
vol. 92
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17.
Arteriolar pulmonary resistance and ventilatory equivalent for oxygen.
[electronic resource]
by
Callol, L
Villegas, F R
Calderon, J
Chillon, M J
Gómez-Terreros, F J
Producer:
19930622
In:
Respiratory medicine
vol. 87
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18.
Microsatellite haplotypes for cystic fibrosis: mutation frameworks and evolutionary tracers.
[electronic resource]
by
Morral, N
Nunes, V
Casals, T
Chillón, M
Giménez, J
Bertranpetit, J
Estivill, X
Producer:
19931004
In:
Human molecular genetics
vol. 2
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19.
ScrfI restriction fragment length polymorphism at the D7S23 locus (probe pKM. 19), closely linked to cystic fibrosis.
[electronic resource]
by
Nunes, V
Ramsay, M
Casals, T
Chillón, M
Lench, N
Schwartz, M
Estivill, X
Producer:
19900501
In:
Nucleic acids research
vol. 18
Online resources:
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20.
Prenatal diagnosis of cystic fibrosis by simultaneous analysis of two different mutations.
[electronic resource]
by
Nunes, V
Gaona, A
Chillon, M
Maña, P
Casals, T
Cutting, G
Estivill, X
Producer:
19920220
In:
Prenatal diagnosis
vol. 11
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