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BMP-3 Dragoon – New IFV version with an unmanned turret which can be armed with a variety of combat modules, including standard BMP-3's Bakhcha-U turret with a 2A70 100 mm cannon, a 2A72 30 mm autocannon and a PKTM 7.62 mm machine gun, the AU-220M Baikal remote weapon station module with a 57 mm BM-57 gun and a module with a 125 mm 2A82-1M ...
The BMP-3 is armed with a 100mm cannon, a 30mm automatic cannon that fires up to 330 rounds a minute, as well as three machine guns. The crew can also fire anti-tank guided missiles through the ...
651 110075 Ensembl ENSG00000152785 ENSMUSG00000029335 UniProt P12645 Q8BHE5 RefSeq (mRNA) NM_001201 NM_173404 NM_001310677 RefSeq (protein) NP_001192 NP_001297606 NP_775580 Location (UCSC) Chr 4: 81.03 – 81.06 Mb Chr 5: 99 – 99.03 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Bone morphogenetic protein 3, also known as osteogenin, is a protein in humans that is encoded by the ...
BMP Global Distribution Inc v Bank of Nova Scotia, a 2008–2009 case in the Supreme Court of Canada; BMP Radio, a broadcasting company based in Houston, Texas; Bruhat Bengaluru Mahanagara Palike (BMP or BBMP), municipal corporation for the city of Bengaluru (Bengalore), India; Boase Massimi Pollitt, a former advertising agency in UK
Implantation of BMP-2 is performed using a variety of biomaterial carriers ("metals, ceramics, polymers, and composites" [17]) and delivery systems ("hydrogel, microsphere, nanoparticles, and fibers" [17]). While used primarily in orthopedic procedures such as spinal fusion, [18] [19] BMP-2 has also found its way into the field of dentistry ...
Bone morphogenetic protein 5 is a protein that in humans is encoded by the BMP5 gene. [5] [6] [7] The protein encoded by this gene is member of the TGFβ superfamily. Bone morphogenetic proteins are known for their ability to induce bone and cartilage development. BMP5 may play a role in certain cancers. Like other BMP's BMP5 is inhibited by ...
The U.S. Preventive Services Task Force said the draft recommendations aim to avoid unnecessary follow-up tests and procedures.
Endoglin, a type I membrane glycoprotein that forms the TGF-beta receptor complex, is a co-receptor of ALK1 for GDF2/BMP-9 binding. Mutations in ALK1 and endoglin cause hereditary hemorrhagic telangiectasia (HHT), a rare but life-threatening genetic disorder that leads to abnormal blood vessel formation in multiple tissues and organs of the body.