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novel dominant negative alpha B - crystallin mutations , Ann Neurol , 2003 , vol(passive) caused byMyofibrillar myopathy
Turn Off Turn On Mutations in myotilincausemyofibrillar myopathy
FLNC / filamin C mutations , Autophagy , 2013(passive) caused bymyofibrillar myopathy
a mutation in the motor domain of mouse MyHC IIb Kurapati , Ramakrishna 2012(passive) caused byMyofibrillar myopathy
myopathies caused by mutations in genescausemyofibrillar myopathy
Selcen D. , Engel A.G. Mutations in myotilincausemyofibrillar myopathy
Engel , Andrew G. / Mutations in myotilincausemyofibrillar myopathy
At least three mutations in the LDB3 gene have been foundto causemyofibrillar myopathy
novel dominant negative aB - crystallin mutations(passive) caused byMyofibrillar myopathy
novel dominant negative alphaB - crystallin mutations(passive) caused byMyofibrillar myopathy
novel dominant negative αB - crystallin mutations(passive) caused byMyofibrillar myopathy
mutations in myotilin , a Z - disk related proteincausemyofibrillar myopathy
Missense mutations in the myotilin - encoding gene ... the molecular defectcan causemyofibrillar myopathy
Myofibrillar myopathy can be caused by mutations in the DES gene Page 2 of 5 More than 40 mutations in the DES gene have been foundto causemyofibrillar myopathy
mutations in FLNC(passive) caused bymyofibrillar myopathy
mutations in ZASP(passive) caused bymyofibrillar myopathy
mutations in BAG3 and Filamin Ccausemyofibrillar myopathy
a mutation in the motor domain of mouse MyHC IIb Kurapati , Ramakrishna McKenna , Caoimhe Carroll , Natalie Laval , Steve Myofibrillar myopathy caused by a mutation in the motor domain of mouse MyHC(passive) caused byMyofibrillar myopathy
Mutations in several genescan causemyofibrillar myopathy
ablation of the bag3 gene(passive) caused bymyofibrillar myopathy
The three different missense mutations in the LDB3 gene ( A147 T , A165V , and R268C ) , recently published by Selcen and Engel , were found in patients in a heterozygous formcausingmyofibrillar myopathy
mutations in the filamin C ( FLNC ) gene(passive) caused bymyofibrillar myopathy
Although various gene mutations have been reportedto causemyofibrillar myopathy
At least five mutations in the MYOT gene have been foundto causemyofibrillar myopathy
a novel FHL1 mutation presenting a mild myopathy with ankle contracture(passive) caused byMyofibrillar myopathy
desmin mutations and characterized by protein aggregates accumulating in muscle fibers(passive) caused bymyofibrillar myopathy
No large deletions or duplications of DES , MYOT , LDB3 , CRYAB , FLNC , or BAG3 have been reportedto causemyofibrillar myopathy
body myopathy ... the molecular defectcan causemyofibrillar myopathy
a mutation in the desmin gene(passive) caused byMyofibrillar myopathy
What chromosomecausesmyofibrillar myopathy
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to the identification of a novel TTN pledto the identification of a novel TTN p
from muscle disuseresultingfrom muscle disuse
to failure of respiratory system and loss of sensation in the limbs ( peripheral neuropathyalso leadsto failure of respiratory system and loss of sensation in the limbs ( peripheral neuropathy
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Page 25 General Introduction 7 primarily of the contractile proteins actin and myosinis composedPage 25 General Introduction 7 primarily of the contractile proteins actin and myosin
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Successful Urban Tech Entrepreneurs |CreatingSuccessful Urban Tech Entrepreneurs |
The Doonie Fund(passive) created byThe Doonie Fund