Publishing research using ab76786? Please let us know so that we can cite the reference in this datasheet.

ab76786 has been referenced in 3 publications.

  • Zhang M  et al. A missense mutation in TMEM67 causes Meckel-Gruber syndrome type 3 (MKS3): a family from China. Int J Clin Exp Pathol 8:5379-86 (2015). PubMed: 26191240
  • Valente EM  et al. Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes. Nat Genet : (2010). ICC/IF ; Human . PubMed: 20512146
  • Romani S  et al. The ciliary proteins Meckelin and Jouberin are required for retinoic acid-dependent neural differentiation of mouse embryonic stem cells. Differentiation 87:134-146 (0). WB . PubMed: 24613594

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