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F Pardo-Manuel

Showing results (11-20 of 26) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|June 1, 1990
Human genes for the alpha and beta chains of complement C4b-binding protein are closely linked in a head-to-tail arrangementF Pardo-Manuel, J Rey-Campos, A Hillarp, et al.
Genetics|January 11, 2000
A genetic test to determine the origin of maternal transmission ratio distortion. Meiotic drive at the mouse Om locusF Pardo-Manuel de Villena, E de la Casa-Esperon, T L Briscoe, et al.
Cytogenetics and Cell Genetics|January 1, 1993
Regional localization of the human vitronectin receptor alpha subunit gene (VNRA) to chromosome 2q31-->q32E Fernández-Ruiz, F Pardo-Manuel de Villena, S Rodríguez de Córdoba, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 15, 2001
H2-haplotype-dependent unequal transmission of the 17(16) translocation chromosome from Ts65Dn femalesJ E Paz-Miguel, F Pardo-Manuel de Villena, P Sánchez-Velasco, et al.
Genomics|July 1, 1993
C4BPAL1, a member of the human regulator of complement activation (RCA) gene cluster that resulted from the duplication of the gene coding for the alpha-chain of C4b-binding proteinP Sánchez-Corral, F Pardo-Manuel de Villena, J Rey-Campos, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 25, 1999
The maternal DDK syndrome phenotype is determined by modifier genes that are not linked to OmF Pardo-Manuel de Villena, E de la Casa-Esperón, A Verner, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 1, 1997
Confirmation of maternal transmission ratio distortion at Om and direct evidence that the maternal and paternal "DDK syndrome" genes are linkedF Pardo-Manuel de Villena, A K Naumova, A E Verner, et al.
Genetics|January 11, 2000
Male-offspring-specific, haplotype-dependent, nonrandom cosegregation of alleles at loci on two mouse chromosomesF Pardo-Manuel de Villena, E de la Casa-Esperon, T L Briscoe, et al.
Genomics|December 1, 1993
The human CD53 gene, coding for a four transmembrane domain protein, maps to chromosomal region 1p13M E Gonzalez, F Pardo-Manuel de Villena, E Fernandez-Ruiz, et al.
Journal of Evolutionary Biology|May 29, 2016
Genetic structure of phenotypic robustness in the collaborative cross mouse diallel panelP N Gonzalez, M Pavlicev, P Mitteroecker, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1990
Human genes for the alpha and beta chains of complement C4b-binding protein are closely linked in a head-to-tail arrangementF Pardo-Manuel, J Rey-Campos, A Hillarp, et al.
Genetics|January 11, 2000
A genetic test to determine the origin of maternal transmission ratio distortion. Meiotic drive at the mouse Om locusF Pardo-Manuel de Villena, E de la Casa-Esperon, T L Briscoe, et al.
Cytogenetics and Cell Genetics|January 1, 1993
Regional localization of the human vitronectin receptor alpha subunit gene (VNRA) to chromosome 2q31-->q32E Fernández-Ruiz, F Pardo-Manuel de Villena, S Rodríguez de Córdoba, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 15, 2001
H2-haplotype-dependent unequal transmission of the 17(16) translocation chromosome from Ts65Dn femalesJ E Paz-Miguel, F Pardo-Manuel de Villena, P Sánchez-Velasco, et al.
Genomics|July 1, 1993
C4BPAL1, a member of the human regulator of complement activation (RCA) gene cluster that resulted from the duplication of the gene coding for the alpha-chain of C4b-binding proteinP Sánchez-Corral, F Pardo-Manuel de Villena, J Rey-Campos, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 25, 1999
The maternal DDK syndrome phenotype is determined by modifier genes that are not linked to OmF Pardo-Manuel de Villena, E de la Casa-Esperón, A Verner, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 1, 1997
Confirmation of maternal transmission ratio distortion at Om and direct evidence that the maternal and paternal "DDK syndrome" genes are linkedF Pardo-Manuel de Villena, A K Naumova, A E Verner, et al.
Genetics|January 11, 2000
Male-offspring-specific, haplotype-dependent, nonrandom cosegregation of alleles at loci on two mouse chromosomesF Pardo-Manuel de Villena, E de la Casa-Esperon, T L Briscoe, et al.
Genomics|December 1, 1993
The human CD53 gene, coding for a four transmembrane domain protein, maps to chromosomal region 1p13M E Gonzalez, F Pardo-Manuel de Villena, E Fernandez-Ruiz, et al.
Journal of Evolutionary Biology|May 29, 2016
Genetic structure of phenotypic robustness in the collaborative cross mouse diallel panelP N Gonzalez, M Pavlicev, P Mitteroecker, et al.
Pageof 3