Associate Professor, Pathology and Lab Medicine, University of Cincinnati College of Medicine
Pathology
Dr. Jun Q. Mo, MD
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Doctor Jun Q. Mo, MD works in the field of Pathology. She studied medicine at University Hospital - University of Cincinnati College of Medicine. Doctor Jun Q. Mo, MD is a published physician as well. She has 19 publications published. The latest was: Maternally inherited diabetes is associated with a homoplasmic T10003C mutation in the mitochondrial tRNA(Gly) gene.
Publications
- Maternally inherited diabetes is associated with a homoplasmic T10003C mutation in the mitochondrial tRNA(Gly) gene.
- Low dose decitabine in very high risk relapsed or refractory acute myeloid leukaemia in children and young adults.
- Salvage therapy of refractory hemophagocytic lymphohistiocytosis with alemtuzumab.
- Maternally inherited essential hypertension is associated with the novel 4263A>G mutation in the mitochondrial tRNAIle gene in a large Han Chinese family.
- Pathology of the liver in familial hemophagocytic lymphohistiocytosis.
- Targeted overexpression of vav3 oncogene in prostatic epithelium induces nonbacterial prostatitis and prostate cancer.
- Fulminant neonatal liver failure in siblings: probable congenital hemophagocytic lymphohistiocytosis.
- The novel A4435G mutation in the mitochondrial tRNAMet may modulate the phenotypic expression of the LHON-associated ND4 G11778A mutation.
- Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced an...
- Clinical evaluation and mitochondrial DNA sequence analysis in three Chinese families with Leber's hereditary optic neuropathy.
- Pediatric hepatic angiosarcoma: case report and review of the literature.
- MALT Lymphoma in Children: Case Report and Review of the Literature.
- GLUT1 endothelial reactivity distinguishes hepatic infantile hemangioma from congenital hepatic vascular malformation with associated capillary proliferation.
- Genetic or pharmacological iron chelation prevents MPTP-induced neurotoxicity in vivo: a novel therapy for Parkinson's disease.
- Maternally transmitted late-onset non-syndromic deafness is associated with the novel heteroplasmic T12201C mutation in the mitochondrial tRNAHis gene.
- The tRNAMet 4435A>G mutation in the mitochondrial haplogroup G2a1 is responsible for maternally inherited hypertension in a Chinese pedigree.
- The mitochondrial tRNA(Thr) A15951G mutation may influence the phenotypic expression of the LHON-associated ND4 G11778A mutation in a Chinese family.
- Vav3 oncogene activates estrogen receptor and its overexpression may be involved in human breast cancer.
Doctors Specialties
- Pediatric Pathology
- Pathology
Accepted Insurances
Education
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Cincinnati Children's Hospital Medical Center -
University Hospital - University of Cincinnati College of Medicine -
Harbor - UCLA Medical Center -
Zhejiang Medical University
Hospital
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Cincinnati Children's Hospital Medical Center
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