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MAX GUAN, DO
DO
Psychiatry Physician
NPI: 1679218796Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Psychiatry PhysicianPrimary
Psychiatry & Neurology — Psychiatry
Code: 2084P0800X
1679218796(CA)
Research & Publications (20)
Aberrant methylation of EphA7 in human prostate cancer and its relation to clinicopathologic features.
PMID 18821581·Int J Cancer·2009
8-other
[Long-term effects of androgen combined with low dose all-trans-retinoic acid on myelodysplastic syndrome: follow-up of 60 cases].
PMID 19671296·Zhonghua Yi Xue Za Zhi·2009
8-other
High-resolution melting analysis for the rapid detection of an intronic single nucleotide polymorphism in SLC22A12 in male patients with primary gout in China.
PMID 19306160·Scand J Rheumatol·2009
4-observational
Bortezomib therapeutic effect is associated with expression of FGFR3 in multiple myeloma cells.
PMID 19331127·Anticancer Res·2009
8-other
Facile preparation method for rare earth phosphate hollow spheres and their photoluminescence properties.
PMID 18582137·Langmuir·2008
8-other
[Comparison of two different methods for establishing nude mouse model bearing osteosarcoma].
PMID 19033102·Nan Fang Yi Ke Da Xue Xue Bao·2008
4-observational
Adenovirus-mediated restoration of expression of the tumor suppressor gene DLC1 inhibits the proliferation and tumorigenicity of aggressive, androgen-independent human prostate cancer cell lines: prospects for gene therapy.
PMID 18369381·Cancer Gene Ther·2008
7-preclinical
A novel cobalt submicro-wire network and its magnetic properties.
PMID 17924382·Chemphyschem·2007
8-other
Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNA(Ser(UCN)) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing loss.
PMID 17698030·Biochem Biophys Res Commun·2007
8-other
Frequency, causes, and new challenges of indeterminate results in Western blot confirmatory testing for antibodies to human immunodeficiency virus.
PMID 17409223·Clin Vaccine Immunol·2007
6-review
Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations.
PMID 16826519·Am J Hum Genet·2006
8-other
Aberrant methylation and deacetylation of deleted in liver cancer-1 gene in prostate cancer: potential clinical applications.
PMID 16533763·Clin Cancer Res·2006
4-observational
Increased efficacy and safety in the treatment of experimental liver cancer with a novel adenovirus-alphavirus hybrid vector.
PMID 16452221·Cancer Res·2006
7-preclinical
[Prevalence of microalbuminuria in type 2 diabetic patients with hypertension].
PMID 15699016·Di Yi Jun Yi Da Xue Xue Bao·2005
8-other
Molecular pathogenetic mechanism of maternally inherited deafness.
PMID 15126302·Ann N Y Acad Sci·2004
7-preclinical
High-performance blue electroluminescent devices based on 2-(4-biphenylyl)-5-(4-carbazole-9-yl)phenyl-1,3,4-oxadiazole.
PMID 14649822·Chem Commun (Camb)·2003
8-other
[Serum uric acid in type 2 diabetic patients complicated by stroke].
PMID 12390852·Di Yi Jun Yi Da Xue Xue Bao·2002
8-other
Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutation.
PMID 11230176·Hum Mol Genet·2001
8-other
A biochemical basis for the inherited susceptibility to aminoglycoside ototoxicity.
PMID 10915767·Hum Mol Genet·2000
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 21810 NORMANDIE AVE FL 1
TORRANCE, CA 90502 - Phone
- (424) 492-3300
Quick Facts
- NPI
- 1679218796
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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