Suchergebnisse - (Person:"Liang, Yanhua")

PubPharm (3)

1

Marie Unna hereditary hypotrichosis : a recurrent c.74C>T mutation in the U2HR gene and literature review

enthalten in: International journal of dermatology | 2014

von Yang, J. | Liang, Y. | Zeng, K. | +2

2

Loss-of-function of SHARPIN causes an osteopenic phenotype in mice

enthalten in: Endocrine | 2011

von Xia, T. | Liang, Y. | Ma, J. | +3

3

Genetic variation of promoter sequence modulates XBP1 expression and genetic risk for vitiligo

enthalten in: PLoS genetics | 2009

von Ren, Y. | Yang, S. | Xu, S. | +14

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