Publicaciones en colaboración con investigadores/as de University of California, San Francisco (13)

2021

  1. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1

    Autophagy, Vol. 17, Núm. 1, pp. 1-382

2005

  1. Targeted disruption of the artemis murine counterpart results in SCID and defective V(D)J recombination that is partially corrected with bone marrow transplantation

    Journal of Immunology, Vol. 174, Núm. 4, pp. 2420-2428

2002

  1. A founder mutation in Artemis, an SNM1-like protein, causes SCID in Athabascan-speaking Native Americans

    Journal of Immunology, Vol. 168, Núm. 12, pp. 6323-6329

1997

  1. Expression of steroid sulfatase during embryogenesis

    Endocrinology, Vol. 138, Núm. 11, pp. 4768-4773

1996

  1. Characterization of the promoter region of human steroid sulfatase: A gene which escapes X inactivation

    Somatic Cell and Molecular Genetics, Vol. 22, Núm. 2, pp. 105-117

  2. Generation of sequence-tagged sites from Xp22.3 by isolating common Alu-PCR products of radiation hybrids retaining overlapping human X chromosome fragments

    Human Genetics, Vol. 97, Núm. 5, pp. 604-610

  3. Genetic mapping of the adenine nucleotide translocase-2 gene (Ant2) to the mouse proximal X chromosome

    Genomics, Vol. 36, Núm. 2, pp. 369-371

1994

  1. An EcoRI RFLP at the D6S509E locus

    Human Molecular Genetics

  2. Isolation and characterization of XE169, a novel human gene that escapes x-inactivation

    Human Molecular Genetics, Vol. 3, Núm. 1, pp. 153-160

  3. Isolation of a new gene GS2 (DXS1283E) from a CpG island between STS and KAL1 on xp22.3

    Genomics, Vol. 22, Núm. 2, pp. 372-376

  4. The murine Xe169 gene escapes X–inactivation like its human homologue

    Nature Genetics, Vol. 7, Núm. 4, pp. 491-496

1993

  1. An evaluation of the inactive mouse X chromosome in somatic cell hybrids

    Somatic Cell and Molecular Genetics, Vol. 19, Núm. 1, pp. 65-71

1992

  1. The human enamel protein gene amelogenin is expressed from both the X and the Y chromosomes

    American Journal of Human Genetics, Vol. 50, Núm. 2, pp. 303-316