Y. Weng

Site-directed Mutagenesis of Human Type X Collagen

J. Bateman, D. Chan, Y. Weng, 1996, The Journal of Biological Chemistry.

Multiexon Deletions in the Type I Collagen COL1A2 Gene in Osteogenesis Imperfecta Type

D. Sillence, S. Mundlos, W. Cole, 1996, The Journal of Biological Chemistry.

The significant role of ATG5 in the maintenance of normal functions of Mc3T3-E1 osteoblast.

H. Chen, J. Kong, Y. Weng, 2018, European review for medical and pharmacological sciences.

Interaction of collagen alpha1(X) containing engineered NC1 mutations with normal alpha1(X) in vitro. Implications for the molecular basis of schmid metaphyseal chondrodysplasia.

J. Bateman, S. Freddi, D. Chan, 1999, The Journal of biological chemistry.

A nonsense mutation in the carboxyl-terminal domain of type X collagen causes haploinsufficiency in schmid metaphyseal chondrodysplasia.

D. Sillence, H. Graham, J. Bateman, 1998, The Journal of clinical investigation.

Identification of a human-specific epitope in a conserved region of the La/SS-B autoantigen.

J. McCluskey, T. Gordon, Y. Weng, 1993, The Journal of clinical investigation.

A type III collagen Gly559 to Arg helix mutation in Ehler's‐Danlos syndrome type IV

E. Haan, J. Bateman, D. Chan, 1998, Human mutation.