Lynn Sakai

Research Professor

  • 13763 Citations
  • 66 h-Index
1982 …2019
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Fingerprint Dive into the research topics where Lynn Sakai is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 7 Similar Profiles
Microfibrils Medicine & Life Sciences
Marfan Syndrome Medicine & Life Sciences
Connective Tissue Medicine & Life Sciences
Transforming Growth Factors Medicine & Life Sciences
Mutation Medicine & Life Sciences
Skin Medicine & Life Sciences
Extracellular Matrix Medicine & Life Sciences
Elastin Medicine & Life Sciences

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Research Output 1982 2019

Fibrillin-1 in the Vasculature: In Vivo Accumulation of eGFP-Tagged Fibrillin-1 in a Knockin Mouse Model

Charbonneau, N. L., Manalo, E. C., Tufa, S. F., Carlson, E. J., Carlberg, V. M., Keene, D. R. & Sakai, L., Jan 1 2019, In : Anatomical Record.

Research output: Contribution to journalArticle

animal models
fluorescence
Fluorescence
Marfan Syndrome
aorta

The acute kidney injury to chronic kidney disease transition in a mouse model of acute cardiorenal syndrome emphasizes the role of inflammation

Matsushita, K., Saritas, T., Eiwaz, M. B., McClellan, N., Coe, I., Zhu, W., Ferdaus, M. Z., Sakai, L. Y., McCormick, J. A. & Hutchens, M. P., Jan 1 2019, (Accepted/In press) In : Kidney International.

Research output: Contribution to journalArticle

Cardio-Renal Syndrome
Cardiopulmonary Resuscitation
Chronic Renal Insufficiency
Acute Kidney Injury
Heart Arrest

Correction: Sex, pregnancy and aortic disease in marfan syndrome(PLoS ONE (2017) 12:7 (e0181166) DOI: 10.1371/journal.pone.0181166)

Renard, M., Muiño-Mosquera, L., Manalo, E. C., Tufa, S., Carlson, E. J., Keene, D. R., Backer, J. D. & Sakai, L., May 1 2018, In : PloS one. 13, 5, e0197631.

Research output: Contribution to journalComment/debate

Open Access
Aortic Diseases
Marfan Syndrome
aorta
pregnancy
Pregnancy
5 Citations (Scopus)

Fibrillin protein pleiotropy: Acromelic dysplasias

Sakai, L. & Keene, D. R., Jan 1 2018, (Accepted/In press) In : Matrix Biology.

Research output: Contribution to journalArticle

Microfibrils
Marfan Syndrome
Mutation
Inborn Genetic Diseases
Proteins

Missense mutation in SLIT2 associated with congenital myopia, anisometropia, connective tissue abnormalities, and obesity

Liu, K. Y., Sengillo, J. D., Velez, G., Jauregui, R., Sakai, L., Maumenee, I. H., Bassuk, A. G., Mahajan, V. B. & Tsang, S. H., Aug 15 2018, In : Orphanet journal of rare diseases. 13, 1, 138.

Research output: Contribution to journalArticle

Open Access
Anisometropia
Myopia
Missense Mutation
Connective Tissue
Obesity