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학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
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논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 발행연도
- 2020.1
- 수록면
- 264 - 266 (3page)
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Dear Editor, High-molecular-weight kininogen (HK) circulates bound to prekallikrein (PK), which can bind to negatively charged phospholipids. It is a non-enzymatic cofactor for kallikrein binding to negatively charged phospholipids. Kallikrein activates factor XII, which then activates factor XI, leading to activation of the intrinsic coagulation pathway [1].
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참고문헌 (10)
참고문헌 신청
Schmaier AH / 2016 / Antithrombotic potential of the contact activation pathway / Curr Opin Hematol 23:445~452
Asmis LM / 2002 / Prekallikrein deficiency: the characteristic normalization of the severely prolonged aPTT following increased preincubation time is due to autoactivation of factor XII / Thromb Res 105:463~470
Fukushima N / 2014 / A novel frameshift mutation in exon 4 causing a deficiency of high-molecular-weight kininogen in a patient with splenic infarction / Intern Med 53:253~257
Richards S / 2015 / Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology / Genet Med 17:405~424
Barco S / 2019 / Detection and differential diagnosis of PK deficiency: genetic study of new families and systematic review of the literature / Hämostaseologie 39:S1~S92
Asmis LM / 2002 / Prekallikrein deficiency: the characteristic normalization of the severely prolonged aPTT following increased preincubation time is due to autoactivation of factor XII / Thromb Res 105:463~470
Fukushima N / 2014 / A novel frameshift mutation in exon 4 causing a deficiency of high-molecular-weight kininogen in a patient with splenic infarction / Intern Med 53:253~257
Richards S / 2015 / Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology / Genet Med 17:405~424
Barco S / 2019 / Detection and differential diagnosis of PK deficiency: genetic study of new families and systematic review of the literature / Hämostaseologie 39:S1~S92
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