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

J Nishimura

Showing results (361-370 of 401) with videos related to

Pageof 41
Sort By:
Blood|May 1, 1997
A patient with paroxysmal nocturnal hemoglobinuria bearing four independent PIG-A mutant clonesJ Nishimura, N Inoue, H Wada, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 19, 2019
Targeted broad-based genetic testing by next-generation sequencing informs diagnosis and facilitates management in patients with kidney diseasesM Adela Mansilla, Ramakrishna R Sompallae, Carla J Nishimura, et al.
Journal of Gastroenterology and Hepatology|August 1, 1996
Case report: primary splenic non-Hodgkin's B cell lymphoma in a patient with chronic hepatitis CT Fukutomi, M Fukushima, Y Tanabe, et al.
American Journal of Medical Genetics. Part A|April 14, 2007
Identification of three novel TECTA mutations in Iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locusNicole C Meyer, Fatemeh Alasti, Carla J Nishimura, et al.
Genome Medicine|June 26, 2014
Copy number variants are a common cause of non-syndromic hearing lossA Eliot Shearer, Diana L Kolbe, Hela Azaiez, et al.
Human Genetics|June 21, 2020
Novel loss-of-function mutations in COCH cause autosomal recessive nonsyndromic hearing lossKevin T Booth, Amama Ghaffar, Muhammad Rashid, et al.
Journal of Gastroenterology and Hepatology|February 24, 2001
Prevalence of hepatitis B or C virus infections in patients with non-Hodgkin's lymphomaM Kuniyoshi, M Nakamuta, H Sakai, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|July 20, 2016
Screening of Living Kidney Donors for Genetic Diseases Using a Comprehensive Genetic Testing StrategyC P Thomas, M A Mansilla, R Sompallae, et al.
Journal of Bone and Mineral Metabolism|October 31, 2001
Diagnostic criteria for primary osteoporosis: year 2000 revisionH Orimo, Y Hayashi, M Fukunaga, et al.
British Journal of Cancer|June 19, 2015
Tumour-suppressive function of SIRT4 in human colorectal cancerM Miyo, H Yamamoto, M Konno, et al.
Pageof 41

Showing results (361-370 of 401) with videos related to

Sort By:
Pageof 41
Blood|May 1, 1997
A patient with paroxysmal nocturnal hemoglobinuria bearing four independent PIG-A mutant clonesJ Nishimura, N Inoue, H Wada, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 19, 2019
Targeted broad-based genetic testing by next-generation sequencing informs diagnosis and facilitates management in patients with kidney diseasesM Adela Mansilla, Ramakrishna R Sompallae, Carla J Nishimura, et al.
Journal of Gastroenterology and Hepatology|August 1, 1996
Case report: primary splenic non-Hodgkin's B cell lymphoma in a patient with chronic hepatitis CT Fukutomi, M Fukushima, Y Tanabe, et al.
American Journal of Medical Genetics. Part A|April 14, 2007
Identification of three novel TECTA mutations in Iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locusNicole C Meyer, Fatemeh Alasti, Carla J Nishimura, et al.
Genome Medicine|June 26, 2014
Copy number variants are a common cause of non-syndromic hearing lossA Eliot Shearer, Diana L Kolbe, Hela Azaiez, et al.
Human Genetics|June 21, 2020
Novel loss-of-function mutations in COCH cause autosomal recessive nonsyndromic hearing lossKevin T Booth, Amama Ghaffar, Muhammad Rashid, et al.
Journal of Gastroenterology and Hepatology|February 24, 2001
Prevalence of hepatitis B or C virus infections in patients with non-Hodgkin's lymphomaM Kuniyoshi, M Nakamuta, H Sakai, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|July 20, 2016
Screening of Living Kidney Donors for Genetic Diseases Using a Comprehensive Genetic Testing StrategyC P Thomas, M A Mansilla, R Sompallae, et al.
Journal of Bone and Mineral Metabolism|October 31, 2001
Diagnostic criteria for primary osteoporosis: year 2000 revisionH Orimo, Y Hayashi, M Fukunaga, et al.
British Journal of Cancer|June 19, 2015
Tumour-suppressive function of SIRT4 in human colorectal cancerM Miyo, H Yamamoto, M Konno, et al.
Pageof 41