Pages that link to "Q39734835"
Jump to navigation
Jump to search
The following pages link to Human embryonic stem cells carrying mutations for severe genetic disorders (Q39734835):
Displaying 32 items.
- Four decades of leading-edge research in the reproductive and developmental sciences: the Infant Primate Research Laboratory at the University of Washington National Primate Research Center (Q33750568) (← links)
- Induced pluripotent stem cells — opportunities for disease modelling and drug discovery (Q34231818) (← links)
- Modelling familial dysautonomia in human induced pluripotent stem cells (Q35088526) (← links)
- Female sex bias in human embryonic stem cell lines. (Q35737463) (← links)
- Molecular mechanisms regulating impaired neurogenesis of fragile X syndrome human embryonic stem cells (Q36141229) (← links)
- Human pluripotent stem cells: applications and challenges in neurological diseases. (Q36193696) (← links)
- The effect of a germline mutation in the APC gene on β-catenin in human embryonic stem cells (Q36232457) (← links)
- Variability in the generation of induced pluripotent stem cells: importance for disease modeling (Q36861680) (← links)
- Clinical Trials in a Dish: The Potential of Pluripotent Stem Cells to Develop Therapies for Neurodegenerative Diseases (Q36904682) (← links)
- Directed differentiation of pluripotent stem cells to kidney cells (Q36969401) (← links)
- Genomic analysis of hESC pedigrees identifies de novo mutations and enables determination of the timing and origin of mutational events (Q37488070) (← links)
- From stem cells to neural networks: recent advances and perspectives for neurodevelopmental disorders (Q37810612) (← links)
- Cardiotoxicity testing using pluripotent stem cell-derived human cardiomyocytes and state-of-the-art bioanalytics: a review. (Q37844011) (← links)
- Modeling neurodevelopmental disorders using human pluripotent stem cells (Q38204302) (← links)
- Human embryonic stem cells carrying an unbalanced translocation demonstrate impaired differentiation into trophoblasts: an in vitro model of human implantation failure (Q38940959) (← links)
- Neural differentiation of Fragile X human Embryonic Stem Cells reveals abnormal patterns of development despite successful neurogenesis. (Q50732939) (← links)
- Mutated Human Embryonic Stem Cells for the Study of Human Genetic Disorders (Q51790660) (← links)
- Lis01_HEFX (Q54902587) (← links)
- Lis02_FXS2 (Q54902588) (← links)
- Lis03_FXS4 (Q54902589) (← links)
- Lis04_Twist1 (Q54902590) (← links)
- Lis05_t(11,22) (Q54902591) (← links)
- Lis06_Gaucher1 (Q54902592) (← links)
- Lis07_AIS1 (Q54902593) (← links)
- Lis08_AIS2 (Q54902863) (← links)
- Lis09_DYS1 (Q54902595) (← links)
- Lis1 (Q54902596) (← links)
- Lis10_DMD1 (Q54902597) (← links)
- Lis11_DMD2 (Q54902598) (← links)
- Lis12_DM1 (Q54902599) (← links)
- Lis13_Alport2 (Q54902600) (← links)
- Lis14_Alport3 (Q54902601) (← links)