Pages that link to "Q74314"
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The following pages link to titin (Q74314):
Displaying 50 items.
- TTN (Q14865286) (← links)
- Ttn (Q14865287) (← links)
- (Q15633882) (redirect page) (← links)
- (Q15633863) (redirect page) (← links)
- (Q15633869) (redirect page) (← links)
- (Q15633857) (redirect page) (← links)
- (Q21991762) (redirect page) (← links)
- Structural basis for activation of the titin kinase domain during myofibrillogenesis (Q22004264) (← links)
- The NH2 terminus of titin spans the Z-disc: its interaction with a novel 19-kD ligand (T-cap) is required for sarcomeric integrity (Q22008009) (← links)
- Titin: a molecular control freak (Q22010365) (← links)
- Titin mutations as the molecular basis for dilated cardiomyopathy (Q24292301) (← links)
- Role of titin in vertebrate striated muscle (Q24292520) (← links)
- Crucial role for Ca2( )/calmodulin-dependent protein kinase-II in regulating diastolic stress of normal and failing hearts via titin phosphorylation (Q24307553) (← links)
- α-Synemin localizes to the M-band of the sarcomere through interaction with the M10 region of titin (Q24307787) (← links)
- Mechanoenzymatics of titin kinase (Q24309951) (← links)
- Atrogin-1 and MuRF1 regulate cardiac MyBP-C levels via different mechanisms (Q24309993) (← links)
- Functional defects of a muscle-specific calpain, p94, caused by mutations associated with limb-girdle muscular dystrophy type 2A (Q24310208) (← links)
- Titins: giant proteins in charge of muscle ultrastructure and elasticity (Q24312140) (← links)
- Molecular structure of the sarcomeric Z-disk: two types of titin interactions lead to an asymmetrical sorting of alpha-actinin. (Q24317266) (← links)
- A human skeletal muscle interactome centered on proteins involved in muscular dystrophies: LGMD interactome (Q24317313) (← links)
- A calmodulin-binding sequence in the C-terminus of human cardiac titin kinase (Q24318437) (← links)
- Multiple molecular interactions implicate the connectin/titin N2A region as a modulating scaffold for p94/calpain 3 activity in skeletal muscle (Q24319118) (← links)
- Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy (Q24319868) (← links)
- Human Autoantibodies Reveal Titin as a Chromosomal Protein (Q24336745) (← links)
- The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy (Q24337914) (← links)
- MURF-1 and MURF-2 target a specific subset of myofibrillar proteins redundantly: towards understanding MURF-dependent muscle ubiquitination (Q28257682) (← links)
- Molecular diversity of myofibrillar proteins: gene regulation and functional significance (Q28277318) (← links)
- The transitional junction: a new functional subcellular domain at the intercalated disc (Q28297685) (← links)
- Induction and myofibrillar targeting of CARP, and suppression of the Nkx2.5 pathway in the MDM mouse with impaired titin-based signaling (Q28585955) (← links)
- Targeted deletion of titin N2B region leads to diastolic dysfunction and cardiac atrophy (Q28587704) (← links)
- M line-deficient titin causes cardiac lethality through impaired maturation of the sarcomere (Q28588265) (← links)
- PINCH2 is a new five LIM domain protein, homologous to PINCHand localized to focal adhesions (Q28589673) (← links)
- A regular pattern of two types of 100-residue motif in the sequence of titin (Q28593289) (← links)
- Null mutation of calpain 3 (p94) in mice causes abnormal sarcomere formation in vivo and in vitro (Q28593842) (← links)
- Mdm muscular dystrophy: interactions with calpain 3 and a novel functional role for titin's N2A domain (Q28863016) (← links)
- Induction of insulin-like growth factor 1 splice forms by subfragments of myofibrillar proteins (Q28910482) (← links)
- Platelet releasate cytosolic proteins [cytosol] (Q50259236) (← links)
- Platelet releasate cytosolic proteins [extracellular region] (Q50259237) (← links)
- M Disk Complex [cytosol] (Q50269786) (← links)
- Z Disk Complex [cytosol] (Q50269808) (← links)
- Genetic screening for the detection of a rare form of cardiomyopathy in a young patient with recurrent syncopes (Q64049626) (← links)
- Evolution of the Highly Repetitive PEVK Region of Titin Across Mammals (Q64105033) (← links)
- Mortality Risk Associated With Truncating Founder Mutations in Titin (Q64108535) (← links)
- Expanding the importance of HMERF titinopathy: new mutations and clinical aspects (Q64232836) (← links)
- Urinary Titin Is Increased in Patients After Cardiac Surgery (Q64244068) (← links)
- Titin-Telethonin complex (Q107514360) (← links)
- Titin-Telethonin complex (Q107602460) (← links)
- User:Pasleim/projectmerge/enwiki-dewiki (← links | edit)
- User:Pasleim/projectmerge/enwiki-svwiki (← links | edit)
- User:Pasleim/projectmerge/cswiki-enwiki (← links | edit)