Chengkang Zhang

Loss-of-function mutation in the <i>prokineticin 2</i> gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism

Nelly Pitteloud, Chengkang Zhang, Duarte Pignatelli et al. · Proceedings of the National Academy of Sciences · 2007 · 263 citations · Full text

Life Sciences, Endocrinology, Genetics +17

Mutations in<i>Prokineticin 2</i>and<i>Prokineticin receptor 2</i>genes in Human Gonadotrophin-Releasing Hormone Deficiency: Molecular Genetics and Clinical Spectrum

Lindsay W. Cole, Yisrael Sidis, Chengkang Zhang et al. · The Journal of Clinical Endocrinology & Metabolism · 2008 · 206 citations · Full text

Medicine, Endocrinology, Molecular Genetics +17

Genetic Overlap in Kallmann Syndrome, Combined Pituitary Hormone Deficiency, and Septo-Optic Dysplasia

Taneli Raivio, Mark J. McCabe, Christopher Romero et al. · The Journal of Clinical Endocrinology & Metabolism · 2012 · 162 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Vasopressin receptor V1a regulates circadian rhythms of locomotor activity and expression of clock-controlled genes in the suprachiasmatic nuclei

Jia‐Da Li, Katherine J. Burton, Chengkang Zhang et al. · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · 2008 · 129 citations · Full text

Life Sciences, Neuroscience, Physiology +16

<i>TRI6</i> and <i>TRI10</i> play different roles in the regulation of deoxynivalenol (DON) production by cAMP signalling in <i>Fusarium graminearum</i>

Cong Jiang, Chengkang Zhang, Chunlan Wu et al. · Environmental Microbiology · 2016 · 115 citations

Life Sciences, Molecular Biology, Plant Biology +17