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C De Silva

Showing results (61-70 of 115) with videos related to

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Cancer|March 1, 1996
Cranial desmoid tumor associated with homozygous inactivation of the adenomatous polyposis coli gene in a 2-year-old girl with familial adenomatous polyposisD C de Silva, M F Wright, D A Stevenson, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|October 6, 2020
Using Biosignals for Objective Measurement of Presence in Virtual Reality EnvironmentsM Athif, B L K Rathnayake, S M D B S Nagahapitiya, et al.
Cryo Letters|May 8, 2018
Association Between DMSO and Sugars in the Sperm Cryopreservation of PacuD M Pires, C D Corcini, A C de Silva, et al.
Physical Review Letters|January 29, 2021
Using Circular Dichroism to Control Energy Transfer in Multiphoton IonizationA H N C De Silva, D Atri-Schuller, S Dubey, et al.
Clinical Laboratory|March 12, 2024
Development of a Low Cost Semiquantitative Polymerase Chain Reaction Assay for Molecular Diagnosis of Williams SyndromeDinali M Ranaweera, Deepthi C de Silva, Duminda Samarasinghe, et al.
Genes & Genetic Systems|January 22, 2025
Development of a TaqMan-based dosage analysis PCR assay for the molecular diagnosis of 22q11.2 deletion syndromeDinali M Ranaweera, Deepthi C de Silva, Duminda Samarasinghe, et al.
RSC Medicinal Chemistry|January 23, 2026
Investigating the role of cytochrome <i>bd</i> oxidases in the antibacterial activity of madecassic acid and derivatives thereofSamantha A Henry, Geraud N Sansom, Thao Thi Phuong Tran, et al.
Transactions of the Royal Society of Tropical Medicine and Hygiene|August 6, 1998
Efficacy of single dose combinations of albendazole, ivermectin and diethylcarbamazine for the treatment of bancroftian filariasisM M Ismail, R L Jayakody, G J Weil, et al.
Journal of Medical Genetics|July 2, 2013
FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactylyNicolas Simonis, Isabelle Migeotte, Nelle Lambert, et al.
Clinical Genetics|June 16, 2015
Congenital generalized lipodystrophy: identification of novel variants and expansion of clinical spectrumA Haghighi, Z Kavehmanesh, A Haghighi, et al.
Pageof 12

Showing results (61-70 of 115) with videos related to

Sort By:
Pageof 12
Cancer|March 1, 1996
Cranial desmoid tumor associated with homozygous inactivation of the adenomatous polyposis coli gene in a 2-year-old girl with familial adenomatous polyposisD C de Silva, M F Wright, D A Stevenson, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|October 6, 2020
Using Biosignals for Objective Measurement of Presence in Virtual Reality EnvironmentsM Athif, B L K Rathnayake, S M D B S Nagahapitiya, et al.
Cryo Letters|May 8, 2018
Association Between DMSO and Sugars in the Sperm Cryopreservation of PacuD M Pires, C D Corcini, A C de Silva, et al.
Physical Review Letters|January 29, 2021
Using Circular Dichroism to Control Energy Transfer in Multiphoton IonizationA H N C De Silva, D Atri-Schuller, S Dubey, et al.
Clinical Laboratory|March 12, 2024
Development of a Low Cost Semiquantitative Polymerase Chain Reaction Assay for Molecular Diagnosis of Williams SyndromeDinali M Ranaweera, Deepthi C de Silva, Duminda Samarasinghe, et al.
Genes & Genetic Systems|January 22, 2025
Development of a TaqMan-based dosage analysis PCR assay for the molecular diagnosis of 22q11.2 deletion syndromeDinali M Ranaweera, Deepthi C de Silva, Duminda Samarasinghe, et al.
RSC Medicinal Chemistry|January 23, 2026
Investigating the role of cytochrome <i>bd</i> oxidases in the antibacterial activity of madecassic acid and derivatives thereofSamantha A Henry, Geraud N Sansom, Thao Thi Phuong Tran, et al.
Transactions of the Royal Society of Tropical Medicine and Hygiene|August 6, 1998
Efficacy of single dose combinations of albendazole, ivermectin and diethylcarbamazine for the treatment of bancroftian filariasisM M Ismail, R L Jayakody, G J Weil, et al.
Journal of Medical Genetics|July 2, 2013
FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactylyNicolas Simonis, Isabelle Migeotte, Nelle Lambert, et al.
Clinical Genetics|June 16, 2015
Congenital generalized lipodystrophy: identification of novel variants and expansion of clinical spectrumA Haghighi, Z Kavehmanesh, A Haghighi, et al.
Pageof 12