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MOLLYANNE BRUNKOW, MD
MD
Family Medicine Physician
NPI: 1487114971IndividualAccepts Medicare
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
04-46796(KS)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
OTHER
Class of 2019
Research & Publications (11)
A point mutation in the murine Hem1 gene reveals an essential role for Hematopoietic protein 1 in lymphopoiesis and innate immunity.
PMID 19015308·J Exp Med·2008
7-preclinical
Polymorphisms in the sclerosteosis/van Buchem disease gene (SOST) region are associated with bone-mineral density in elderly whites.
PMID 15514891·Am J Hum Genet·2004
8-other
A novel mutation in CD83 results in the development of a unique population of CD4+ T cells.
PMID 15322158·J Immunol·2004
7-preclinical
Osteocyte control of bone formation via sclerostin, a novel BMP antagonist.
PMID 14633986·EMBO J·2003
7-preclinical
A 52-kb deletion in the SOST-MEOX1 intergenic region on 17q12-q21 is associated with van Buchem disease in the Dutch population.
PMID 12116252·Am J Med Genet·2002
8-other
The amount of scurfin protein determines peripheral T cell number and responsiveness.
PMID 11714795·J Immunol·2001
7-preclinical
A rare polyadenylation signal mutation of the FOXP3 gene (AAUAAA-->AAUGAA) leads to the IPEX syndrome.
PMID 11685453·Immunogenetics·2001
8-other
Bone dysplasia sclerosteosis results from loss of the SOST gene product, a novel cystine knot-containing protein.
PMID 11179006·Am J Hum Genet·2001
5-case
Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse.
PMID 11138001·Nat Genet·2001
7-preclinical
The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3.
PMID 11137993·Nat Genet·2001
7-preclinical
X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy.
PMID 11137992·Nat Genet·2001
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
- 15101 GLENWOOD AVE
STANLEY, KS 66223 - Phone
- (913) 681-8866
Quick Facts
- NPI
- 1487114971
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 7
- Publications
- 11
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