Physician
Pathology
Dr. Olga B. Boican-Roche, MD
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Olga Boican Roche works in the field of Pathology. Dr. Olga B. Boican-Roche is also a published physician. He has 19 publication published. The most recent publication is: Transcriptional regulation of genes via hypoxia-inducible factor.
Publications
- Ligand-protein database: linking protein-ligand complex structures to binding data.
- New VMD2 gene mutations identified in patients affected by Best vitelliform macular dystrophy.
- Identification of novel VMD2 gene mutations in patients with best vitelliform macular dystrophy.
- [Hereditary angioedema of delayed onset].
- Chemotherapy induces NEDP1-mediated destabilization of MDM2.
- Regulation of endocytosis via the oxygen-sensing pathway.
- Transcriptional regulation of genes via hypoxia-inducible factor.
- SERPING1 mutations in 59 families with hereditary angioedema.
- Loss of JAK2 regulation via a heterodimeric VHL-SOCS1 E3 ubiquitin ligase underlies Chuvash polycythemia.
- Deregulation of E2-EPF ubiquitin carrier protein in papillary renal cell carcinoma.
- SATB2 augments ÎNp63α in head and neck squamous cell carcinoma.
- Oxygen-independent degradation of HIF-alpha via bioengineered VHL tumour suppressor complex.
- First case of homozygous C1 inhibitor deficiency.
- VHL promotes E2 box-dependent E-cadherin transcription by HIF-mediated regulation of SIP1 and snail.
- Hereditary angioedema: the mutation spectrum of SERPING1/C1NH in a large Spanish cohort.
- Hereditary angioedema due to C1 inhibitor deficiency: patient registry and approach to the prevalence in Spain.
- Hereditary and acquired angioedema: problems and progress: proceedings of the third C1 esterase inhibitor deficiency workshop and beyond.
- Detection of C1 inhibitor (SERPING1/C1NH) mutations in exon 8 in patients with hereditary angioedema: evidence for 10 novel mutations.
Doctors Specialties
- Family Medicine
- Pathology
Accepted Insurances
Education
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Loma Linda University -
Carol Davila University of Medicine and Pharmacy
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