| HUMAN:ACE | 2012-02-12 03:01:pm CST | GO:0007519 - skeletal muscle tissue development (P) | PMID:21956137 | IGI | The ACE I and ACTN3 X alleles determine speed and power for Lithuanian athletes. Table 3 shows that Lithuanian athletes who are carriers
of the ACE I/I and I/D as well as ACTN3 X/X and R/X genotypes have the potential to achieve better results in power-requiring sports
| challenge |
| RAT:GDF8 | 2012-02-12 05:10:pm CST | GO:0014732 - skeletal muscle atrophy (P) | PMID:22033906 | IEP | Figure 2 shows that the wet weight ratio(size) of the gastrocnemius muscle is at its lowest when the circulating myostatin levels are at their highest, in terms of days after injury.
| challenge |
| RAT:FST | 2012-02-08 07:16:pm CST | GO:0014732 - skeletal muscle atrophy (P) | PMID:22033906 | IDA | Findings show follistatin expression increased during recovery phase of post-denervated muscle atrophy. Follistatin/Myostatin ratio can be used to track muscle recovery post nerve injury. Figure 3.
| challenge |
| CAPHI:CASA1 | 2012-02-09 06:00:pm CST | GO:0048518 - positive regulation of biological process (P) | PMID:21864407 | IMP | Figure 2. Figure 3. Shows SNP14 in CSN1S1 results in increased milk production.
| challenge |
| CAPHI:CASA1 | 2012-02-09 06:06:pm CST | GO:0065007 - biological regulation (P) | PMID:21864407 | IMP | Figure 2. Figure 3. Shows SNP14 of CSN1S1 results in decreased protein % in milk.
| challenge |
| CAPHI:CASA1 | 2012-02-09 06:08:pm CST | GO:0065007 - biological regulation (P) | PMID:21864407 | IMP | Figure 2. Figure 3. Shows SNP14 of CSN1S1 results in decreased fat % in milk.
| challenge |
| MOUSE:GDF8 | 2012-02-12 05:15:pm CST | GO:0048632 - negative regulation of skeletal muscle growth (P) | PMID:21390326 | IMP | Table 1 and Figure 2 show the Gastrocnemius, Quadriceps, and Triceps muscles all were significantly larger in weight(g) in myostatin deficient mice compared to normal myostatin mice.
| challenge |
| HUMAN:ACTN3 | 2012-02-12 03:01:pm CST | GO:0007519 - skeletal muscle tissue development (P) | PMID:21956137 | IGI | The ACE I and ACTN3 X alleles determine speed and power for Lithuanian athletes. Table 3 shows that Lithuanian athletes who are carriers of the ACE I/I and I/D as well as ACTN3 X/X and R/X genotypes have the potential to achieve better results in power-requiring sports
| challenge |
| HUMAN:ACE | 2012-02-12 02:36:pm CST | GO:0007519 - skeletal muscle tissue development (P) | PMID:21956137 | IMP | Table 2 shows male and female athletes with the ACE I/I genotype had higher handgrip strength and
STEMP compared with male and female athletes having the ACE D/D genotype.
| challenge |
| MOUSE:GDF8 | 2012-02-12 03:56:pm CST | GO:0019222 - regulation of metabolic process (P) | PMID:11877467 | IMP | Table 2 shows Mstn–/– mice had higher rates of total and resting O2 consumption compared with Mstn+/+ mice, which is expected given the higher body weights of Mstn–/– mice. If the data are expressed as a function of body weight, however, Mstn–/– mice actually had lower rates of total and resting O2 consumption compared with Mstn+/+ mice.
| challenge |
| MOUSE:GDF8 | 2012-02-12 05:00:pm CST | GO:0019217 - regulation of fatty acid metabolic process (P) | PMID:21390326 | IMP | Figure 4 shows mg fatty acids per g of muscle tissue is significantly less in myostatin depleted mice fed a high-fat diet.
| challenge |
| MOUSE:GDF8 | 2012-02-12 05:00:pm CST | GO:0043610 - regulation of carbohydrate utilization (P) | PMID:21390326 | IMP | Figure 3 shows blood glucose concentration is significantly lower in myostatin depleted mice fed a high-fat diet for 5 months, 90 min after ip glucose injection.
| challenge |
| MOUSE:GDF8 | 2012-02-12 04:58:pm CST | | PMID:21390326 | IMP | Figure 5 shows that myostatin depleted mice have a significantly lower incidence and severity of hepatic statosis when fed a high-fat diet for 5 months.
| challenge |
| MOUSE:GDF8 | 2012-02-12 05:34:pm CST | GO:0048632 - negative regulation of skeletal muscle growth (P) | PMID:11877467 | IMP | Figure 1a shows the increased mass of triceps muscle in Mstn -/- mice at different ages as well as an apparent dose-dependency on muscle mass.
| challenge |
| MOUSE:GDF8 | 2012-02-12 05:54:pm CST | GO:0019216 - regulation of lipid metabolic process (P) | PMID:11877467 | IMP | Figure 1b-g shows the significant differences in fat pad mass between Mstn -/- and Mstn +/+ mice after 2 months of age.
| challenge |
| MOUSE:M3K5 | 2012-02-22 12:43:pm CST | GO:0045663 - positive regulation of myoblast differentiation (P) | PMID:22337877 | IDA | | challenge |
| MOUSE:NR2C2 | 2012-02-22 12:47:pm CST | GO:0045663 - positive regulation of myoblast differentiation (P) | PMID:22337877 | IDA | | challenge |
| MOUSE:M3K5 | 2012-02-22 06:10:pm CST | GO:0038066 - p38MAPK cascade (P) | PMID:22337877 | IEP | | challenge |
| MOUSE:NR2C2 | 2012-02-22 06:12:pm CST | GO:0038066 - p38MAPK cascade (P) | PMID:22337877 | IEP | | challenge |
| MOUSE:DLX3 | 2012-02-23 11:39:pm CST | GO:0071895 - odontoblast differentiation (P) | PMID:22351765 | IMP | | challenge |
| MOUSE:DLX3 | 2012-02-23 11:43:pm CST | GO:0070468 - dentin secretion (P) | PMID:22351765 | IMP | | challenge |
| ECOBW:RRMF | 2012-02-26 05:28:pm CST | GO:2000234 - positive regulation of rRNA processing (P) | PMID:20807199 | IEP | | challenge |
| MOUSE:CADH1 | 2012-03-09 06:32:pm CST | GO:0035847 - uterine epithelium development (P) | PMID:22378759 | IMP | | challenge |
| MOUSE:CADH1 | 2012-03-09 06:32:pm CST | GO:0007566 - embryo implantation (P) | PMID:22378759 | IMP | | challenge |
| MOUSE:CADH1 | 2012-03-09 06:32:pm CST | GO:0046697 - decidualization (P) | PMID:22378759 | IMP | | challenge |
| ARATH:PUB13 | 2012-03-09 08:46:pm CST | GO:0043066 - negative regulation of apoptosis (P) | PMID:22383540 | IMP | | challenge |
| ARATH:PUB13 | 2012-03-09 08:46:pm CST | GO:2000028 - regulation of photoperiodism, flowering (P) | PMID:22383540 | IMP | Fig. 7. Results were most notable in MD exposure. Negative regulator of flowering.
| challenge |
| DROME:Q0KHV6 | 2012-03-18 02:42:pm CDT | GO:0047497 - mitochondrion transport along microtubule (P) | PMID:22396657 | IMP | | challenge |
| DROME:Q0KHV6 | 2012-03-18 02:42:pm CDT | GO:0048312 - intracellular distribution of mitochondria (P) | PMID:22396657 | IMP | | challenge |
| MOUSE:MNS1 | 2012-03-18 03:00:pm CDT | GO:0007283 - spermatogenesis (P) | PMID:22396656 | IMP | | challenge |
| MOUSE:MNS1 | 2012-03-18 03:00:pm CDT | GO:0045724 - positive regulation of flagellum assembly (P) | PMID:22396656 | IMP | | challenge |
| MOUSE:MNS1 | 2012-03-18 03:00:pm CDT | GO:0031514 - motile cilium (C) | PMID:22396656 | IMP | | challenge |
| MOUSE:IRF1 | 2012-03-18 03:30:pm CDT | GO:0001556 - oocyte maturation (P) | PMID:22384442 | IDA | | challenge |
| MOUSE:ABHD5 | 2012-03-18 03:54:pm CDT | GO:0050996 - positive regulation of lipid catabolic process (P) | PMID:22383684 | IMP | | challenge |
| HUMAN:UTP6 | 2012-04-01 05:15:pm CDT | GO:0015935 - small ribosomal subunit (C) | PMID:22434888 | IEP | | challenge |
| HUMAN:UTP6 | 2012-04-01 05:15:pm CDT | GO:0046601 - positive regulation of centriole replication (P) | PMID:22434888 | IEP | | challenge |
| HELPX:P94832 | 2012-04-15 11:28:am CDT | GO:0052058 - modification by symbiont of host morphology or physiology via substance secreted by type IV secretion system (P) | PMID:22493745 | IMP | | challenge |
| HELPX:P94832 | 2012-04-15 11:28:am CDT | GO:0030255 - protein secretion by the type IV secretion system (P) | PMID:22493745 | IPI | | challenge |
| RAT:D3ZRK7 | 2012-04-15 11:51:am CDT | GO:0043293 - apoptosome (C) | PMID:22493447 | IPI | | challenge |
| MOUSE:Q8CGC3 | 2012-04-15 12:29:pm CDT | GO:0090044 - positive regulation of tubulin deacetylation (P) | PMID:22492994 | IEP | | challenge |
| MOUSE:SWI5 | 2012-04-15 12:50:pm CDT | GO:0000730 - DNA recombinase assembly (P) | PMID:22492707 | IEP | Fig. 2 shows that the SWI5-SFR1 complex functions in stabilization of the Rad51 filament
| challenge |
| MOUSE:SFR1 | 2012-04-15 12:53:pm CDT | GO:0000730 - DNA recombinase assembly (P) | PMID:22492707 | IEP | Fig. 2 shows the SWI5-SFR1 complex functions in stabilizing the Rad51 filament
| challenge |