| Health / Medical Topics |
Kallmann Syndrome
An X-linked or autosomal dominant genetic syndrome characterized by hypogonadotropic hypogonadism and anosmia. (NCI Thesaurus)
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Kallikrein-2 (261 aa, ~29 kDa) is encoded by the human KLK2 gene. This protein plays a role in proteolysis and vasodilation. …
Kallikrein-15 (256 aa, ~28 kDa) is encoded by the human KLK15 gene. This protein is involved in proteolysis.
Kallikrein-11 (282 aa, ~31 kDa) is encoded by the human KLK11 gene. This protein plays a role in peptide metabolism.
Kallikrein-10 (276 aa, ~30 kDa) is encoded by the human KLK10 gene. This protein plays a role in both the mediation of…
One Kallikrein Inhibitor Unit is identical to the quantity of protease inhibitor (eg, aprotinin) that has the ability to inhibit two kallikrein…
An arbitrary unit of a kallikrein inactivator concentration equal to the concentration at which one milliliter of the mixture contains one unit…
