Miller Lab

Latest News

Miller Lab attends first annual FSHD Canada Event

-Thursday, April 25th, 2013

Friends of FSH Research Auction Raises over $175,000

-Wednesday, February 13th, 2013

Annual FiSHing for a Cure Auction! Save the date.

-Saturday, January 26th, 2013

Miller Lab featured in UW News

-Tuesday, November 20th, 2012

Platform development for candidate drug screening for FSHD

-Tuesday, July 24th, 2012

New FSHD Publication from the Miller Lab!

-Monday, April 23rd, 2012

Our Read-Feed

The cell biology of disease: Cellular and molecular mechanisms underlying muscular...

miR-411 is up-regulated in FSHD myoblasts and suppresses myogenic factors.

HiveBio is Working to Become Seattle's First Community Biology Lab (Video)

Human inactive X chromosome is compacted through a PRC2-independent SMCHD1-HBiX1...

Recreational and household physical activity at different time points and DNA global...

Reevaluating measures of disease progression in facioscapulohumeral muscular dystrophy.

Muscle regeneration and inflammation in patients with facioscapulohumeral muscular...

Latest Publications

Lemmers, R.J.L.F., Tawil, R., et al, "Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2", Nature Genetics, 44:p.1370-1374, 2012

van der Maarel S.M., Miller D.G., Tawil R., Filippova G.N., et al, "Facioscapulohumeral muscular dystrophy: consequences of chromatin relaxation", Current Opinion in Neurology, 25:p.614-620, 2012

Lemmers R.J.L.F., Miller D.G., van der Maarel S.M., "Facioscapulohumeral Muscular Dystrophy", GeneReviews at GeneTests, Medical Genetics Information Resource:p.[database online], 2012

Block G.J., Petek L.M., Narayanan D., Amell A.M., et al, "Asymmetric Bidirectional Transcription from the FSHD-Causing D4Z4 Array Modulates DUX4 Production", PLoS ONE, 7:p.e35532, 2012

Upcoming Events

Contact

millab@uw.edu
815 Mercer St N-411,Box 358056

Seattle WA 98109