LIP1, a cytoplasmic protein functionally linked to the Peutz-Jeghers syndrome kinase LKB1. Read more about LIP1, a cytoplasmic protein functionally linked to the Peutz-Jeghers syndrome kinase LKB1.
Genetic variation in the human urea transporter-2 is associated with variation in blood pressure. Read more about Genetic variation in the human urea transporter-2 is associated with variation in blood pressure.
Excessive CpG island hypermethylation in cancer cell lines versus primary human malignancies. Read more about Excessive CpG island hypermethylation in cancer cell lines versus primary human malignancies.
BACE knockout mice are healthy despite lacking the primary beta-secretase activity in brain: implications for Alzheimer's disease therapeutics. Read more about BACE knockout mice are healthy despite lacking the primary beta-secretase activity in brain: implications for Alzheimer's disease therapeutics.
The mouse Peutz-Jeghers syndrome gene Lkb1 encodes a nuclear protein kinase. Read more about The mouse Peutz-Jeghers syndrome gene Lkb1 encodes a nuclear protein kinase.
LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation. Read more about LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation.
De novo mutations (GAG deletion) in the DYT1 gene in two non-Jewish patients with early-onset dystonia. Read more about De novo mutations (GAG deletion) in the DYT1 gene in two non-Jewish patients with early-onset dystonia.
The human FXY gene is located within Xp22.3: implications for evolution of the mammalian X chromosome. Read more about The human FXY gene is located within Xp22.3: implications for evolution of the mammalian X chromosome.
Liposome-medicated gene transfer and expression via the skin. Read more about Liposome-medicated gene transfer and expression via the skin.
Intronic point mutation in the IL2RG gene causing X-linked severe combined immunodeficiency. Read more about Intronic point mutation in the IL2RG gene causing X-linked severe combined immunodeficiency.
