Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Arijit Biswas

Showing results (141-150 of 179) with videos related to

Pageof 18
Sort By:
Human Mutation|November 24, 2021
GGCX variants leading to biallelic deficiency to γ-carboxylate GRP cause skin laxity in VKCFD1 patientsSuvoshree Ghosh, Katrin Kraus, Arijit Biswas, et al.
Journal of Thrombosis and Haemostasis : JTH|October 13, 2023
Heterozygosity in factor XIII genes and the manifestation of mild inherited factor XIII deficiencySneha Singh, Behnaz Pezeshkpoor, Muhammad Ahmer Jamil, et al.
Birth (Berkeley, Calif.)|February 18, 2018
Trends and predictors of cesarean birth in Singapore, 2005-2014: A population-based cohort studyClaudia Chi, Deanette Pang, Izzuddin M Aris, et al.
Blood|October 24, 2024
Cryo-EM structure of the human native plasma coagulation factor XIII complexSneha Singh, Gregor Hagelueken, Deniz Ugurlar, et al.
Journal of Thrombosis and Haemostasis : JTH|February 16, 2021
GGCX mutations show different responses to vitamin K thereby determining the severity of the hemorrhagic phenotype in VKCFD1 patientsSuvoshree Ghosh, Katrin Kraus, Arijit Biswas, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 19, 2019
Characterization of the mutation spectrum in a Pakistani cohort of type 3 von Willebrand diseaseShariq Ahmed, Hamideh Yadegari, Arshi Naz, et al.
Fetal Diagnosis and Therapy|January 21, 2019
Fetoscopic versus Ultrasound-Guided Intravascular Delivery of Maternal Bone Marrow Cells in Fetal Macaques: A Technical Model for Intrauterine Haemopoietic Cell TransplantationCitra N Z Mattar, Yi-Wan Tan, Nuryanti Johana, et al.
American Journal of Physiology. Heart and Circulatory Physiology|September 15, 2018
Human fetal hearts with tetralogy of Fallot have altered fluid dynamics and forcesHadi Wiputra, Ching Kit Chen, Elias Talbi, et al.
Haematologica|February 25, 2010
Identification of eight novel coagulation factor XIII subunit A mutations: implied consequences for structure and functionVytautas Ivaskevicius, Arijit Biswas, Carville Bevans, et al.
Journal of Gastroenterology and Hepatology|May 15, 2015
Hepatic differentiation of human amniotic epithelial cells and in vivo therapeutic effect on animal model of cirrhosisJaymie Siqi Lin, Lei Zhou, Antony Sagayaraj, et al.
Pageof 18

Showing results (141-150 of 179) with videos related to

Sort By:
Pageof 18
Human Mutation|November 24, 2021
GGCX variants leading to biallelic deficiency to γ-carboxylate GRP cause skin laxity in VKCFD1 patientsSuvoshree Ghosh, Katrin Kraus, Arijit Biswas, et al.
Journal of Thrombosis and Haemostasis : JTH|October 13, 2023
Heterozygosity in factor XIII genes and the manifestation of mild inherited factor XIII deficiencySneha Singh, Behnaz Pezeshkpoor, Muhammad Ahmer Jamil, et al.
Birth (Berkeley, Calif.)|February 18, 2018
Trends and predictors of cesarean birth in Singapore, 2005-2014: A population-based cohort studyClaudia Chi, Deanette Pang, Izzuddin M Aris, et al.
Blood|October 24, 2024
Cryo-EM structure of the human native plasma coagulation factor XIII complexSneha Singh, Gregor Hagelueken, Deniz Ugurlar, et al.
Journal of Thrombosis and Haemostasis : JTH|February 16, 2021
GGCX mutations show different responses to vitamin K thereby determining the severity of the hemorrhagic phenotype in VKCFD1 patientsSuvoshree Ghosh, Katrin Kraus, Arijit Biswas, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 19, 2019
Characterization of the mutation spectrum in a Pakistani cohort of type 3 von Willebrand diseaseShariq Ahmed, Hamideh Yadegari, Arshi Naz, et al.
Fetal Diagnosis and Therapy|January 21, 2019
Fetoscopic versus Ultrasound-Guided Intravascular Delivery of Maternal Bone Marrow Cells in Fetal Macaques: A Technical Model for Intrauterine Haemopoietic Cell TransplantationCitra N Z Mattar, Yi-Wan Tan, Nuryanti Johana, et al.
American Journal of Physiology. Heart and Circulatory Physiology|September 15, 2018
Human fetal hearts with tetralogy of Fallot have altered fluid dynamics and forcesHadi Wiputra, Ching Kit Chen, Elias Talbi, et al.
Haematologica|February 25, 2010
Identification of eight novel coagulation factor XIII subunit A mutations: implied consequences for structure and functionVytautas Ivaskevicius, Arijit Biswas, Carville Bevans, et al.
Journal of Gastroenterology and Hepatology|May 15, 2015
Hepatic differentiation of human amniotic epithelial cells and in vivo therapeutic effect on animal model of cirrhosisJaymie Siqi Lin, Lei Zhou, Antony Sagayaraj, et al.
Pageof 18