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MARY SHIMANE, DMD
DMD
Dentist
NPI: 1851848196Individual
Specialties, Licenses & Credentials
DentistPrimary
Dentist
Code: 122300000X
46564(CA)
Research & Publications (15)
Pilot study of a dissection table for gross anatomy laboratory equipped with a photocatalytic device that decomposes formaldehyde.
PMID 18075210·J Occup Health·2007
8-other
Gene expression profiling of the rat endometriosis model.
PMID 17845203·Am J Reprod Immunol·2007
7-preclinical
Detection of gamma-aminobutyric acid-induced glutamate release in acute mouse hippocampal slices with a patch sensor.
PMID 16620752·Anal Biochem·2006
7-preclinical
Two subclasses of lung squamous cell carcinoma with different gene expression profiles and prognosis identified by hierarchical clustering and non-negative matrix factorization.
PMID 16007138·Oncogene·2005
4-observational
Integrated classification of lung tumors and cell lines by expression profiling.
PMID 12218176·Proc Natl Acad Sci U S A·2002
8-other
Role of Lkb1, the causative gene of Peutz-Jegher's syndrome, in embryogenesis and polyposis.
PMID 12060709·Proc Natl Acad Sci U S A·2002
7-preclinical
Pancreatic exocrine damage induced by subcutaneous injection of a low dosage of zinc.
PMID 11817687·Biol Trace Elem Res·2001
7-preclinical
Molecular and physiological evidence for multifunctionality of carnitine/organic cation transporter OCTN2.
PMID 11160873·Mol Pharmacol·2001
7-preclinical
Molecular and functional characterization of organic cation/carnitine transporter family in mice.
PMID 11010964·J Biol Chem·2000
7-preclinical
Molecular identification and characterization of novel members of the human organic anion transporter (OATP) family.
PMID 10873595·Biochem Biophys Res Commun·2000
8-other
Phenotype-dependent expression of cadherin 6B in vascular and visceral smooth muscle cells.
PMID 10708758·FEBS Lett·2000
7-preclinical
No evidence of Peutz-Jeghers syndrome gene LKB1 involvement in left-sided colorectal carcinomas.
PMID 10676634·Cancer Res·2000
8-other
Identification and characterization of BPTF, a novel bromodomain transcription factor.
PMID 10662542·Genomics·2000
8-other
Two novel missense mutations of the OCTN2 gene (W283R and V446F) in a patient with primary systemic carnitine deficiency.
PMID 10612840·Hum Mutat·2000
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 20099 REDWOOD RD
CASTRO VALLEY, CA 94546 - Phone
- (510) 881-1611
Quick Facts
- NPI
- 1851848196
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 15
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