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  2. Bone morphogenetic protein - Wikipedia

    en.wikipedia.org/wiki/Bone_morphogenetic_protein

    As such, disruption of BMP signaling can affect the body plan of the developing embryo. For example, BMP4 and its inhibitors noggin and chordin help regulate polarity of the embryo (i.e. back to front patterning). Specifically BMP-4 and its inhibitors play a major role in neurulation and the development of the neural plate.

  3. Bone morphogenetic protein 3 - Wikipedia

    en.wikipedia.org/wiki/Bone_morphogenetic_protein_3

    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 ...

  4. Noggin (protein) - Wikipedia

    en.wikipedia.org/wiki/Noggin_(protein)

    Noggin is a signaling molecule that plays an important role in promoting somite patterning in the developing embryo. [8] It is released from the notochord and regulates bone morphogenic protein 4 (BMP4) during development. [9] The absence of BMP4 will cause the patterning of the neural tube and somites from the neural plate in the developing ...

  5. Fibrodysplasia ossificans progressiva - Wikipedia

    en.wikipedia.org/wiki/Fibrodysplasia_ossificans...

    Fibrodysplasia ossificans progressiva (/ ˌ f aɪ b r oʊ d ɪ ˈ s p l eɪ ʒ (i) ə ɒ ˈ s ɪ f ɪ k æ n z p r ə ˈ ɡ r ɛ s ɪ v ə /; [1] abbr. FOP), also called Münchmeyer disease or formerly myositis ossificans progressiva, is an extremely rare connective tissue disease in which fibrous connective tissue such as muscle, tendons, and ligaments turn into bone tissue (ossification).

  6. Bone morphogenetic protein receptor - Wikipedia

    en.wikipedia.org/wiki/Bone_morphogenetic_protein...

    Type 1 contains a glycine-serine-rich domain to be phosphorylated by type 2 kinase domain, initiating the signaling transduction pathway of the SMAD signaling cascade. [3] The wrist epitope motif on BMP-2 has a high-affinity binding site for BMPR-IA. The knuckle epitope motif on BMP-2 has a low-affinity binding site for BMPR-II. [4]

  7. BMPR1B - Wikipedia

    en.wikipedia.org/wiki/BMPR1B

    BMPR1B is the major transducer of signals in these condensations as demonstrated in experiments using constitutively active BMPR1B receptors. [9] BMPR1B is a more effective transducer of GDF5 than BMPR1A. [9] Unlike BMPR1A null mice, which die at an early embryonic stage, BMPR1B null mice are viable. [9]

  8. GDF10 - Wikipedia

    en.wikipedia.org/wiki/GDF10

    GDF10 belongs to the transforming growth factor beta superfamily that is closely related to bone morphogenetic protein-3 . It plays a role in head formation and may have multiple roles in skeletal morphogenesis. [5] [6] GDF10 is also known as BMP-3b, with GDF10 and BMP3 regarded as a separate subgroup within the TGF-beta superfamily. [5]

  9. BMPR2 - Wikipedia

    en.wikipedia.org/wiki/BMPR2

    BMPR2 is expressed on both human and animal granulosa cells, and is a crucial receptor for bone morphogenetic protein 15 (BMP15) and growth differentiation factor 9 (GDF9). ). These two protein signaling molecules and their BMPR2-mediated effects play an important role in follicle development in preparation for ovulatio