BackgroundRett syndrome (RTT), a common cause of mental retardation in girls, is associated with mutations in the MECP2 gene. Most human cases of MECP2 mutation in girls result in classical or variant forms of RTT. When these same mutations occur in males, they often present as severe neonatal encephalopathy. However, some MECP2 mutations can also lead to diseases characterized as mental ...
PubMed Central
... is a member of the Mouse Models of Human Cancer ... SYMPOSIA, CLINICAL MEDICINE, NEOPLASMS, PERIPHERAL NEUROPATHY, STRAINS ...
DTIC Science & Technology
... TITLE: Development of a Mouse Model for Determination of the Role of the Catechol Metabolites of Estradiol in Mammary Tumorigenesis ...
... Title : Development of a Mouse Model for Determination of the Role of the Catechol Metabolites of Estradiol in Mammary Tumorigenesis. ...
... Crossing the TRAMP mouse with the PSCA-TVA transgenic mouse has resulted in the TRAMP-TVA mouse that is destined to develop prostate ...
... Crossing the TRAMP mouse with the PSCA-TVA transgenic mouse has resulted in the TRAMP-TVA mouse, which allows for efficient and specific ...
