Pages that link to "Q36225015"

The following pages link to Lethal thalassemia after insertional disruption of the mouse major adult beta-globin gene (Q36225015):

Displaying 37 items.

• Animal models of β-hemoglobinopathies: utility and limitations (Q28067142) (← links)
• Impaired motor coordination in mice lacking prion protein (Q28292921) (← links)
• 7-Dehydrocholesterol-dependent proteolysis of HMG-CoA reductase suppresses sterol biosynthesis in a mouse model of Smith-Lemli-Opitz/RSH syndrome (Q28354262) (← links)
• Hypertension, cardiac hypertrophy, and sudden death in mice lacking natriuretic peptide receptor A (Q28511919) (← links)
• Unexpected embryonic stem (ES) cell mutations represent a concern in gene targeting: lessons from "fierce" mice (Q28513855) (← links)
• A mouse model for beta 0-thalassemia (Q28587408) (← links)
• Antisickling property of fetal hemoglobin enhances nitric oxide bioavailability and ameliorates organ oxidative stress in transgenic-knockout sickle mice (Q33686611) (← links)
• Substitution of the human beta-spectrin promoter for the human agamma-globin promoter prevents silencing of a linked human beta-globin gene in transgenic mice (Q33781540) (← links)
• Mouse model of human beta zero thalassemia: targeted deletion of the mouse beta maj- and beta min-globin genes in embryonic stem cells (Q33895206) (← links)
• Iron overload cardiomyopathy: better understanding of an increasing disorder (Q34165921) (← links)
• Spatial organization of gene expression: the active chromatin hub. (Q34230157) (← links)
• Effect of fetal hemoglobin on microvascular regulation in sickle transgenic-knockout mice (Q34359790) (← links)
• The human desmin locus: gene organization and LCR-mediated transcriptional control (Q34503087) (← links)
• Role of L-type Ca2+ channels in iron transport and iron-overload cardiomyopathy (Q36444526) (← links)
• Use of mouse models to study the mechanisms and consequences of RBC clearance. (Q36632113) (← links)
• Deletion and replacement of the mouse adult beta-globin genes by a "plug and socket" repeated targeting strategy (Q36668182) (← links)
• Heme degradation and oxidative stress in murine models for hemoglobinopathies: thalassemia, sickle cell disease and hemoglobin C disease (Q36812858) (← links)
• Humanized Mouse Model of Cooley's Anemia (Q37099192) (← links)
• Preclinical transfusion-dependent humanized mouse model of beta thalassemia major. (Q37187563) (← links)
• IL-2 pathway blocking in combination with anti-CD154 synergistically establishes mixed macrochimerism with limited dose of bone marrow cells and prolongs skin graft survival in mice (Q37292014) (← links)
• Regulation of iron absorption in hemoglobinopathies. (Q37320318) (← links)
• Non-invasive MRI biomarkers for the early assessment of iron overload in a humanized mouse model of β-thalassemia. (Q37668169) (← links)
• Cardiac complications in beta-thalassemia: From mice to men. (Q38686059) (← links)
• Knockouts. Targeting the mouse genome: a compendium of knockouts (Part I) (Q40409394) (← links)
• Mechanisms of developmental control of transcription in the murine alpha- and beta-globin loci (Q40442072) (← links)
• Embryonic lethality, decreased erythropoiesis, and defective octamer-dependent promoter activation in Oct-1-deficient mice. (Q40468947) (← links)
• Accumulation of gamma-globin mRNA and induction of erythroid differentiation after treatment of human leukaemic K562 cells with tallimustine (Q40794098) (← links)
• Transgenic animals: how they are made and their role in animal production and research (Q41004106) (← links)
• A common disease-associated missense mutation in alpha-sarcoglycan fails to cause muscular dystrophy in mice (Q41823092) (← links)
• Genetic decreases in atrial natriuretic peptide and salt-sensitive hypertension (Q42280521) (← links)
• A humanized BAC transgenic/knockout mouse model for HbE/beta-thalassemia (Q45857661) (← links)
• Long-term correction of beta-thalassemia with minimal cellular requirement and transplantation modalities (Q50693964) (← links)
• Efficient repetitive alteration of the mouse Huntington's disease gene by management of background in the tag and exchange gene targeting strategy (Q77567177) (← links)
• A humanized mouse model for a common beta0-thalassemia mutation (Q81551600) (← links)
• Humanized mouse models of Cooley's anemia: correct fetal-to-adult hemoglobin switching, disease onset, and disease pathology (Q84745387) (← links)
• Animal Models of Normal and Disturbed Iron and Copper Metabolism (Q90028577) (← links)
• Minihepcidins improve ineffective erythropoiesis and splenomegaly in a new mouse model of adult beta-thalassemia major (Q90466673) (← links)