Growth performance of male rabbits with long-term supplementation of CLA. by A. M. Abdelatty (7485983)

Effect of long term dietary CLA supplementation on sperm kinetics¹. by A. M. Abdelatty (7485983)

Sperm concentration, serum testosterone, and some testicular metabolites of CLA fed male rabbits. by A. M. Abdelatty (7485983)

Effect of long-term CLA supplementation on testicular epithelium thickness and lesion scoring of rabbit testicle “Johnsen's scoring system”. by A. M. Abdelatty (7485983)

“…<p>Long term of dietary CLA supplementation decreased testicular epithelium thickness at a dose dependent manner (5a) but induced testicular degeneration (5b) in CLA 1% group only.…”

Effect of long-term CLA supplementation on epididymal fat globules “stained with Sudan black”. by A. M. Abdelatty (7485983)

Chemical composition of the experimental diets (g/kg DM). by A. M. Abdelatty (7485983)

Effect of long-term CLA supplementation on rabbit epididymis. by A. M. Abdelatty (7485983)

Effect of long term CLA supplementation on testicular tissue of rabbit. by A. M. Abdelatty (7485983)

“…<p>Normal histological structure in CON group (4a) Vacuolation of Sertoli cells and decreased spermatogenesis in CLA 0.5% group (4b). …”

Application of single step genomic BLUP under different uncertain paternity scenarios using simulated data by Rafael Lara Tonussi (4476496)

“…The simulated genome had a total length of 2,333 cM, containing 735,293 biallelic markers and 7,000 QTLs randomly distributed over the 29 BTA. …”

Maternal separation (MS) did not affect the quantal size (<i>q</i>). by Jesús David Ayala-Rodríguez (17364296)

MOF-Derived Hollow Heterostructure MnCo₂O₄@Co₉S₈ Nanocages as a High-Performance Bifunctional Electrode for Water Electrolysis and Flexi... by Rui Yuan (615737)

“…The activity of the overall water-splitting electrolyzer did not decrease significantly even in alkaline simulated seawater, which means that it has a resistance to chlorine corrosion. …”

Image_5_Spliceostatin C, a component of a microbial bioherbicide, is a potent phytotoxin that inhibits the spliceosome.jpg by Joanna Bajsa-Hirschel (3902302)

“…In silico binding studies showed that SPC binds to a pocket between the SF3B3 and PF5A of the spliceosome.…”

Table_5_Spliceostatin C, a component of a microbial bioherbicide, is a potent phytotoxin that inhibits the spliceosome.docx by Joanna Bajsa-Hirschel (3902302)

“…In silico binding studies showed that SPC binds to a pocket between the SF3B3 and PF5A of the spliceosome.…”

Lysine 50 of Tat regulates expression of C5, CRLF2, APBA1, and BDNF genes. by Loreto Carvallo (4167607)

“…<p>THP-1Tat-Flag and THP-1Tat K50ATat-Flag cell lines (generated from independent experiments described in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0179882#pone.0179882.g005" target="_blank">Fig 5</a>) were differentiated to macrophages with PMA for 24 and 48 hours. …”

Variation of MLR of concrete under three curing conditions after F–T: (a) standard curing; (b) 5 °C curing; (c) −3 °C curing. by YongHe Liu (20477123)

Example of fold increases and decreases in expression between developmental stages (blue, based on (<i>X</i>_<i>t+1</i><i>-X</i>_<i>t</i>) / <i>min</i> [<i>X</i... by Frances Trail (647410)

DNA binding and transcriptional consequence of Arid3a-Arid3b interaction. by Jeffrey L. Kurkewich (3044211)

Data underlying Figs 1B, 1C, 1E, 1J, 1K, 2B, 2C, 2E, 2F, 2H, 2I, 3B, 3C, 3D, 3E, 3F, 4B, 4D, 4E, 4F, 4G, 5A, 5B, 6E and 6G. by Xinxin Li (281237)

S1 Fig - by Amelia Kate Pollard (3164691)

The map was generated by five different models to show snakebite occurrence in Chattogram Division. by Mohammad Abdul Wahed Chowdhury (18585669)