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LAWRENCE KARNISKI, MD
MD
Nephrology Physician
NPI: 1952399891Individual
Specialties, Licenses & Credentials
Internal Medicine Physician
Internal Medicine
Code: 207R00000X
24877(IA)
Nephrology PhysicianPrimary
Internal Medicine — Nephrology
Code: 207RN0300X
24877(IA)
Research & Publications (11)
Functional expression and cellular distribution of diastrophic dysplasia sulfate transporter (DTDST) gene mutations in HEK cells.
PMID 15294877·Hum Mol Genet·2004
8-other
Formate-stimulated NaCl absorption in the proximal tubule is independent of the pendrin protein.
PMID 12372770·Am J Physiol Renal Physiol·2002
7-preclinical
Mutations in the diastrophic dysplasia sulfate transporter (DTDST) gene: correlation between sulfate transport activity and chondrodysplasia phenotype.
PMID 11448940·Hum Mol Genet·2001
4-observational
Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms?
PMID 19204907·Hum Mutat·2009
7-preclinical
The Slc26a4 transporter functions as an electroneutral Cl-/I-/HCO3- exchanger: role of Slc26a4 and Slc26a6 in I- and HCO3- secretion and in regulation of CFTR in the parotid duct.
PMID 18565999·J Physiol·2008
7-preclinical
Regulation of anion exchanger Slc26a6 by protein kinase C.
PMID 17151144·Am J Physiol Cell Physiol·2007
7-preclinical
A compound heterozygote harboring novel and recurrent DTDST mutations with intermediate phenotype between atelosteogenesis type II and diastrophic dysplasia.
PMID 16642506·Am J Med Genet A·2006
5-case
Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations.
PMID 11317356·Hum Mutat·2001
8-other
Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretion.
PMID 11274445·Proc Natl Acad Sci U S A·2001
7-preclinical
Functional differences of the PDS gene product are associated with phenotypic variation in patients with Pendred syndrome and non-syndromic hearing loss (DFNB4).
PMID 10861298·Hum Mol Genet·2000
7-preclinical
Human pendrin expressed in Xenopus laevis oocytes mediates chloride/formate exchange.
PMID 10644529·Am J Physiol Cell Physiol·2000
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 200 HAWKINS DR
IOWA CITY, IA 52242 - Phone
- (319) 356-3971
Quick Facts
- NPI
- 1952399891
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 11
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