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  2. ACVR1 - Wikipedia

    en.wikipedia.org/wiki/ACVR1

    The typical FOP patient has the amino acid arginine substituted for the amino acid histidine at position 206 in this protein. [10] [11] This causes a change in the critical glycine-serine activation domain of the protein which will cause the protein to bind its inhibitory ligand (FKBP12) less tightly, and thus over-activate the BMP/SMAD pathway ...

  3. 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]

  4. Bone morphogenetic protein - Wikipedia

    en.wikipedia.org/wiki/Bone_morphogenetic_protein

    Bone morphogenetic proteins (BMPs) are a group of growth factors also known as cytokines and as metabologens. [1] Professor Marshall Urist and Professor Hari Reddi discovered their ability to induce the formation of bone and cartilage, BMPs are now considered to constitute a group of pivotal morphogenetic signals, orchestrating tissue architecture throughout the body.

  5. Bone morphogenetic protein 4 - Wikipedia

    en.wikipedia.org/wiki/Bone_morphogenetic_protein_4

    Bone morphogenetic protein 4 is a protein that in humans is encoded by BMP4 gene. [4] [5] BMP4 is found on chromosome 14q22-q23. BMP4 is a member of the bone morphogenetic protein family which is part of the transforming growth factor-beta superfamily. The superfamily includes large families of growth and differentiation factors. BMP4 is highly ...

  6. 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).

  7. Repulsive guidance molecule A - Wikipedia

    en.wikipedia.org/wiki/Repulsive_guidance_molecule_A

    Repulsive guidance molecule A (RGMa) is a bone morphogenetic protein (BMP) co-receptor of the repulsive guidance molecule family. Together with BMPR1A and BMPR1B, as well as ACVR2A and BMPR2, it binds BMPs thereby activating the intracellular SMAD1/5/8 signalling pathway. [5] In humans this protein is encoded by the RGMA gene. [6]

  8. 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

  9. Bone morphogenetic protein 1 - Wikipedia

    en.wikipedia.org/wiki/Bone_morphogenetic_protein_1

    Bone morphogenetic protein 1, also known as BMP1, is a protein which in humans is encoded by the BMP1 gene. [ 5 ] [ 6 ] There are seven isoforms of the protein created by alternate splicing . Function