https://journals.plos.org/plosgenetics/article?id=10.1371/journal.pgen.0020175
Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2 |...
Kallmann syndrome combines anosmia, related to defective olfactory bulb morphogenesis, and hypogonadism due to gonadotropin-releasing hormone deficiency....
kallmann syndromein themutations
https://www.mdpi.com/2077-0383/12/13/4330
Prokineticin 2 and Cytokine Content in the Synovial Fluid of Knee Osteoarthritis and Traumatic...
Knee osteoarthritis (OA) is a chronic degenerative inflammatory-based condition caused by a cascade of different intra-articular molecules including several...
https://journals.plos.org/plosgenetics/article/authors?id=10.1371/journal.pgen.0020175
Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2 |...
Kallmann syndrome combines anosmia, related to defective olfactory bulb morphogenesis, and hypogonadism due to gonadotropin-releasing hormone deficiency....
kallmann syndromein themutations
https://research.monash.edu/en/publications/prokineticin-1-signaling-and-gene-regulation-in-early-human-pregn/
Prokineticin 1 signaling and gene regulation in early human pregnancy - Monash University
gene regulation
https://iris.cnr.it/handle/20.500.14243/415913
Prokineticin 2/PROK2 and Male Infertility
maleinfertility