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L Boon

Showing results (101-110 of 114) with videos related to

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Frontiers in Immunology|March 14, 2025
The gut-brain-axis one year after treatment with cladribine tablets in patients with relapsing remitting multiple sclerosis: a pilot studyJeske van Pamelen, Carla Rodriguez-Mogeda, Lynn van Olst, et al.
Mucosal Immunology|November 5, 2015
miR-511-3p, embedded in the macrophage mannose receptor gene, contributes to intestinal inflammationS E M Heinsbroek, M L Squadrito, R Schilderink, et al.
American Journal of Human Genetics|July 1, 1996
Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13Y Gong, M Vikkula, L Boon, et al.
Human Genetics|April 2, 2008
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformationNisha Limaye, N Revencu, N Van Regemorter, et al.
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformationNisha Limaye, N Revencu, N Van Regemorter, et al.
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformationNisha Limaye, N Revencu, N Van Regemorter, et al.
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformationNisha Limaye, N Revencu, N Van Regemorter, et al.
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformationNisha Limaye, N Revencu, N Van Regemorter, et al.
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformationNisha Limaye, N Revencu, N Van Regemorter, et al.
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformationNisha Limaye, N Revencu, N Van Regemorter, et al.
Pageof 12

Showing results (101-110 of 114) with videos related to

Sort By:
Pageof 12
Frontiers in Immunology|March 14, 2025
The gut-brain-axis one year after treatment with cladribine tablets in patients with relapsing remitting multiple sclerosis: a pilot studyJeske van Pamelen, Carla Rodriguez-Mogeda, Lynn van Olst, et al.
Mucosal Immunology|November 5, 2015
miR-511-3p, embedded in the macrophage mannose receptor gene, contributes to intestinal inflammationS E M Heinsbroek, M L Squadrito, R Schilderink, et al.
American Journal of Human Genetics|July 1, 1996
Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13Y Gong, M Vikkula, L Boon, et al.
Human Genetics|April 2, 2008
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformationNisha Limaye, N Revencu, N Van Regemorter, et al.
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformationNisha Limaye, N Revencu, N Van Regemorter, et al.
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformationNisha Limaye, N Revencu, N Van Regemorter, et al.
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformationNisha Limaye, N Revencu, N Van Regemorter, et al.
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformationNisha Limaye, N Revencu, N Van Regemorter, et al.
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformationNisha Limaye, N Revencu, N Van Regemorter, et al.
Human Genetics|April 3, 2008
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformationNisha Limaye, N Revencu, N Van Regemorter, et al.
Pageof 12