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Showing results (51-60 of 76) with videos related to

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Human Molecular Genetics|October 4, 2017
Liver cyst gene knockout in cholangiocytes inhibits cilium formation and Wnt signalingEdgar S Wills, René H M Te Morsche, Jeroen van Reeuwijk, et al.
Oncogene|January 13, 2006
Interplay between VHL/HIF1alpha and Wnt/beta-catenin pathways during colorectal tumorigenesisR H Giles, M P Lolkema, C M Snijckers, et al.
Ophthalmology|June 17, 2015
Blindness and Visual Impairment in the Republic of SurinameJanna Minderhoud, Jerrel C Pawiroredjo, Herman C I Themen, et al.
The British Journal of Ophthalmology|November 13, 2016
The cataract situation in Suriname: an effective intervention programme to increase the cataract surgical rate in a developing countryJerrel C Pawiroredjo, Janna Minderhoud, Dennis R A Mans, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 11, 2012
Rapid angiogenesis onset after discontinuation of sunitinib treatment of renal cell carcinoma patientsArjan W Griffioen, Laurie A Mans, Annemarie M A de Graaf, et al.
American Journal of Human Genetics|September 7, 2010
Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndromeChristian Gilissen, Heleen H Arts, Alexander Hoischen, et al.
The American Journal of Tropical Medicine and Hygiene|May 5, 2012
First case of cutaneous leishmaniasis caused by Leishmania (Viannia) braziliensis in SurinameRicardo V P F Hu, Alida D Kent, Emily R Adams, et al.
Human Molecular Genetics|October 2, 2008
Usher syndrome and Leber congenital amaurosis are molecularly linked via a novel isoform of the centrosomal ninein-like proteinErwin van Wijk, Ferry F J Kersten, Aileen Kartono, et al.
Clinical and Experimental Dermatology|December 10, 2015
Monitoring the response of patients with cutaneous leishmaniasis to treatment with pentamidine isethionate by quantitative real-time PCR, and identification of Leishmania parasites not responding to therapyD R A Mans, A D Kent, R V Hu, et al.
Journal of Medical Genetics|March 8, 2011
C14ORF179 encoding IFT43 is mutated in Sensenbrenner syndromeHeleen H Arts, Ernie M H F Bongers, Dorus A Mans, et al.
Pageof 8

Showing results (51-60 of 76) with videos related to

Sort By:
Pageof 8
Human Molecular Genetics|October 4, 2017
Liver cyst gene knockout in cholangiocytes inhibits cilium formation and Wnt signalingEdgar S Wills, René H M Te Morsche, Jeroen van Reeuwijk, et al.
Oncogene|January 13, 2006
Interplay between VHL/HIF1alpha and Wnt/beta-catenin pathways during colorectal tumorigenesisR H Giles, M P Lolkema, C M Snijckers, et al.
Ophthalmology|June 17, 2015
Blindness and Visual Impairment in the Republic of SurinameJanna Minderhoud, Jerrel C Pawiroredjo, Herman C I Themen, et al.
The British Journal of Ophthalmology|November 13, 2016
The cataract situation in Suriname: an effective intervention programme to increase the cataract surgical rate in a developing countryJerrel C Pawiroredjo, Janna Minderhoud, Dennis R A Mans, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 11, 2012
Rapid angiogenesis onset after discontinuation of sunitinib treatment of renal cell carcinoma patientsArjan W Griffioen, Laurie A Mans, Annemarie M A de Graaf, et al.
American Journal of Human Genetics|September 7, 2010
Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndromeChristian Gilissen, Heleen H Arts, Alexander Hoischen, et al.
The American Journal of Tropical Medicine and Hygiene|May 5, 2012
First case of cutaneous leishmaniasis caused by Leishmania (Viannia) braziliensis in SurinameRicardo V P F Hu, Alida D Kent, Emily R Adams, et al.
Human Molecular Genetics|October 2, 2008
Usher syndrome and Leber congenital amaurosis are molecularly linked via a novel isoform of the centrosomal ninein-like proteinErwin van Wijk, Ferry F J Kersten, Aileen Kartono, et al.
Clinical and Experimental Dermatology|December 10, 2015
Monitoring the response of patients with cutaneous leishmaniasis to treatment with pentamidine isethionate by quantitative real-time PCR, and identification of Leishmania parasites not responding to therapyD R A Mans, A D Kent, R V Hu, et al.
Journal of Medical Genetics|March 8, 2011
C14ORF179 encoding IFT43 is mutated in Sensenbrenner syndromeHeleen H Arts, Ernie M H F Bongers, Dorus A Mans, et al.
Pageof 8