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Eddie Ip

Showing results (21-30 of 27) with videos related to

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BMC Infectious Diseases|May 5, 2006
The interferon gamma gene polymorphism +874 A/T is associated with severe acute respiratory syndromeWai Po Chong, W K Eddie Ip, Gloria Hoi Wan Tso, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 9, 2018
Identification of clinically actionable variants from genome sequencing of families with congenital heart diseaseDimuthu Alankarage, Eddie Ip, Justin O Szot, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|July 10, 2008
Low serum mannose-binding lectin level increases the risk of death due to pneumococcal infectionDamon P Eisen, Melinda M Dean, Marja A Boermeester, et al.
The Journal of Infectious Diseases|April 20, 2005
Mannose-binding lectin in severe acute respiratory syndrome coronavirus infectionW K Eddie Ip, Kwok Hung Chan, Helen K W Law, et al.
Iscience|February 22, 2024
Single cell atlas of human gastric muscle immune cells and macrophage-driven changes in idiopathic gastroparesisLakshmikanth L Chikkamenahalli, Erik Jessen, Cheryl E Bernard, et al.
Human Molecular Genetics|December 4, 2020
Heterozygous loss of WBP11 function causes multiple congenital defects in humans and miceElla M M A Martin, Annabelle Enriquez, Duncan B Sparrow, et al.
The New England Journal of Medicine|August 10, 2017
NAD Deficiency, Congenital Malformations, and Niacin SupplementationHongjun Shi, Annabelle Enriquez, Melissa Rapadas, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
BMC Infectious Diseases|May 5, 2006
The interferon gamma gene polymorphism +874 A/T is associated with severe acute respiratory syndromeWai Po Chong, W K Eddie Ip, Gloria Hoi Wan Tso, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 9, 2018
Identification of clinically actionable variants from genome sequencing of families with congenital heart diseaseDimuthu Alankarage, Eddie Ip, Justin O Szot, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|July 10, 2008
Low serum mannose-binding lectin level increases the risk of death due to pneumococcal infectionDamon P Eisen, Melinda M Dean, Marja A Boermeester, et al.
The Journal of Infectious Diseases|April 20, 2005
Mannose-binding lectin in severe acute respiratory syndrome coronavirus infectionW K Eddie Ip, Kwok Hung Chan, Helen K W Law, et al.
Iscience|February 22, 2024
Single cell atlas of human gastric muscle immune cells and macrophage-driven changes in idiopathic gastroparesisLakshmikanth L Chikkamenahalli, Erik Jessen, Cheryl E Bernard, et al.
Human Molecular Genetics|December 4, 2020
Heterozygous loss of WBP11 function causes multiple congenital defects in humans and miceElla M M A Martin, Annabelle Enriquez, Duncan B Sparrow, et al.
The New England Journal of Medicine|August 10, 2017
NAD Deficiency, Congenital Malformations, and Niacin SupplementationHongjun Shi, Annabelle Enriquez, Melissa Rapadas, et al.
Pageof 3