Pages that link to "Q34472144"
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The following pages link to Somatic mosaicism in Fanconi anemia: evidence of genotypic reversion in lymphohematopoietic stem cells. (Q34472144):
Displaying 50 items.
- Molecular pathogenesis and clinical management of Fanconi anemia (Q24621696) (← links)
- Fanconi anaemia (Q24678530) (← links)
- Diagnosis of Fanconi Anemia: Chromosomal Breakage Analysis (Q27495962) (← links)
- Modeling Human Bone Marrow Failure Syndromes Using Pluripotent Stem Cells and Genome Engineering (Q28083303) (← links)
- The emerging genetic and molecular basis of Fanconi anaemia (Q28199075) (← links)
- Mechanisms and consequences of somatic mosaicism in humans (Q28205052) (← links)
- Republished: Non-heritable genetics of human disease: spotlight on post-zygotic genetic variation acquired during lifetime (Q28385687) (← links)
- Non-heritable genetics of human disease: spotlight on post-zygotic genetic variation acquired during lifetime (Q28392579) (← links)
- Hematopoietic dysfunction in a mouse model for Fanconi anemia group D1 (Q28585929) (← links)
- The genomics of inherited bone marrow failure: from mechanism to the clinic. (Q30235895) (← links)
- Disease-corrected haematopoietic progenitors from Fanconi anaemia induced pluripotent stem cells. (Q30489278) (← links)
- Current diagnosis of inherited bone marrow failure syndromes (Q33374981) (← links)
- Genetic predisposition to myelodysplastic syndrome and acute myeloid leukemia in children and young adults (Q33428604) (← links)
- CRISPR/Cas9-Mediated Correction of the FANCD1 Gene in Primary Patient Cells (Q33838956) (← links)
- Knockdown of Fanconi anemia genes in human embryonic stem cells reveals early developmental defects in the hematopoietic lineage (Q33839812) (← links)
- Preclinical correction of human Fanconi anemia complementation group A bone marrow cells using a safety-modified lentiviral vector (Q34082330) (← links)
- The Fanconi anemia group C gene product: signaling functions in hematopoietic cells. (Q34466465) (← links)
- Comparison of chromosome breakage in non-mosaic and mosaic patients with Fanconi anemia, relatives, and patients with other inherited bone marrow failure syndromes (Q34475544) (← links)
- Concise review: preleukemic stem cells: molecular biology and clinical implications of the precursors to leukemia stem cells (Q34647637) (← links)
- Second-site mutation in the Wiskott-Aldrich syndrome (WAS) protein gene causes somatic mosaicism in two WAS siblings (Q34984944) (← links)
- Bone marrow failure syndromes in children (Q34995965) (← links)
- Stem cell gene therapy for fanconi anemia: report from the 1st international Fanconi anemia gene therapy working group meeting. (Q35086128) (← links)
- In vivo reversion to normal of inherited mutations in humans (Q35440872) (← links)
- Diagnosis of Fanconi anemia by diepoxybutane analysis (Q35534473) (← links)
- Unrelated donor bone marrow transplantation for the treatment of Fanconi anemia (Q35642826) (← links)
- Fanconi anaemia and leukaemia - clinical and molecular aspects (Q35828191) (← links)
- Deficiency of UBE2T, the E2 Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi Anemia (Q35836818) (← links)
- Natural gene therapy in monozygotic twins with Fanconi anemia (Q35849565) (← links)
- Survival of the fittest: in vivo selection and stem cell gene therapy (Q36306141) (← links)
- Reversion mutations in patients with leukocyte adhesion deficiency type-1 (LAD-1) (Q36384593) (← links)
- The concept and practice of Fanconi Anemia: from the clinical bedside to the laboratory bench (Q36508235) (← links)
- An update on the management of severe idiopathic aplastic anaemia in children (Q36703904) (← links)
- Overnight transduction with foamyviral vectors restores the long-term repopulating activity of Fancc-/- stem cells (Q37001945) (← links)
- A comprehensive strategy for the subtyping of patients with Fanconi anaemia: conclusions from the Spanish Fanconi Anemia Research Network (Q37004779) (← links)
- Somatic mosaicism in Wiskott--Aldrich syndrome suggests in vivo reversion by a DNA slippage mechanism. (Q37111771) (← links)
- Myelodysplasia and acute leukemia as late complications of marrow failure: future prospects for leukemia prevention. (Q37229440) (← links)
- Fanconi anemia and its diagnosis (Q37344270) (← links)
- Phenotypic correction of Fanconi anemia cells in the murine bone marrow after carrier cell mediated delivery of lentiviral vector (Q37424081) (← links)
- Human brain harbors single nucleotide somatic variations in functionally relevant genes possibly mediated by oxidative stress (Q37605380) (← links)
- Patient-specific naturally gene-reverted induced pluripotent stem cells in recessive dystrophic epidermolysis bullosa (Q37707008) (← links)
- Concise review: Transplantation of human hematopoietic cells for extracellular matrix protein deficiency in epidermolysis bullosa (Q37873887) (← links)
- Current insights into inherited bone marrow failure syndromes (Q38248285) (← links)
- Genetic counseling for Fanconi anemia: crosslinking disciplines. (Q38252487) (← links)
- Rapid Lentiviral Transduction Preserves the Engraftment Potential of Fanca-/- Hematopoietic Stem Cells (Q38971720) (← links)
- Revertant mosaicism in genodermatoses (Q39123627) (← links)
- How I manage patients with Fanconi anaemia. (Q39285296) (← links)
- Sleeping Beauty-mediated correction of Fanconi anemia type C. (Q39505168) (← links)
- Lentiviral-mediated genetic correction of hematopoietic and mesenchymal progenitor cells from Fanconi anemia patients (Q39508334) (← links)
- Stem cell collection and gene transfer in Fanconi anemia (Q40260881) (← links)
- A rapid method for retrovirus-mediated identification of complementation groups in Fanconi anemia patients. (Q40387870) (← links)