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

L Oligny

Showing results (31-40 of 40) with videos related to

Pageof 4
Sort By:
You have reached the last page of results.This site can display upto 40 results.
Human Molecular Genetics|November 18, 1998
3-Hydroxy-3-methylglutaryl-CoA lyase (HL): gene targeting causes prenatal lethality in HL-deficient miceS P Wang, J D Marth, L L Oligny, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|April 20, 1999
A two-tier polymerase chain reaction direct sequencing method for detecting and typing human papillomaviruses in pathological specimensJ C Feoli-Fonseca, L L Oligny, M Filion, et al.
The Journal of Pediatrics|February 15, 2001
Molecular characterization of a pediatric pheochromocytoma with suspected bilateral diseaseH Mircescu, F Wilkin, J Paquette, et al.
Obesity Research|April 24, 2001
The adipose tissue phenotype of hormone-sensitive lipase deficiency in miceS P Wang, N Laurin, J Himms-Hagen, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|June 3, 2006
Exaggerated vasomotor response to ANG II in rats with fetal programming of hypertension associated with exposure to a low-protein diet during gestationC Yzydorczyk, F Gobeil, G Cambonie, et al.
The Journal of Clinical Endocrinology and Metabolism|October 30, 2008
Lethal respiratory failure and mild primary hypothyroidism in a term girl with a de novo heterozygous mutation in the TITF1/NKX2.1 geneEmilie Maquet, Sabine Costagliola, Jasmine Parma, et al.
Histopathology|May 13, 2010
High level of apoptosis and low AKT activation in mass screening as opposed to standard neuroblastomaHervé Sartelet, Shigeru Ohta, Stephane Barrette, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|September 9, 2022
Workload Measurement in Subspecialty Placental Pathology in CanadaJames R Wright, Suzanne Chan, Eric K Morgen, et al.
Human Genetics|November 6, 2019
Association of rare non-coding SNVs in the lung-specific FOXF1 enhancer with a mitigation of the lethal ACDMPV phenotypePrzemyslaw Szafranski, Qian Liu, Justyna A Karolak, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2017
Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesisSarah Boissel, Catherine Fallet-Bianco, David Chitayat, et al.
Pageof 4

Showing results (31-40 of 40) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
Human Molecular Genetics|November 18, 1998
3-Hydroxy-3-methylglutaryl-CoA lyase (HL): gene targeting causes prenatal lethality in HL-deficient miceS P Wang, J D Marth, L L Oligny, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|April 20, 1999
A two-tier polymerase chain reaction direct sequencing method for detecting and typing human papillomaviruses in pathological specimensJ C Feoli-Fonseca, L L Oligny, M Filion, et al.
The Journal of Pediatrics|February 15, 2001
Molecular characterization of a pediatric pheochromocytoma with suspected bilateral diseaseH Mircescu, F Wilkin, J Paquette, et al.
Obesity Research|April 24, 2001
The adipose tissue phenotype of hormone-sensitive lipase deficiency in miceS P Wang, N Laurin, J Himms-Hagen, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|June 3, 2006
Exaggerated vasomotor response to ANG II in rats with fetal programming of hypertension associated with exposure to a low-protein diet during gestationC Yzydorczyk, F Gobeil, G Cambonie, et al.
The Journal of Clinical Endocrinology and Metabolism|October 30, 2008
Lethal respiratory failure and mild primary hypothyroidism in a term girl with a de novo heterozygous mutation in the TITF1/NKX2.1 geneEmilie Maquet, Sabine Costagliola, Jasmine Parma, et al.
Histopathology|May 13, 2010
High level of apoptosis and low AKT activation in mass screening as opposed to standard neuroblastomaHervé Sartelet, Shigeru Ohta, Stephane Barrette, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|September 9, 2022
Workload Measurement in Subspecialty Placental Pathology in CanadaJames R Wright, Suzanne Chan, Eric K Morgen, et al.
Human Genetics|November 6, 2019
Association of rare non-coding SNVs in the lung-specific FOXF1 enhancer with a mitigation of the lethal ACDMPV phenotypePrzemyslaw Szafranski, Qian Liu, Justyna A Karolak, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2017
Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesisSarah Boissel, Catherine Fallet-Bianco, David Chitayat, et al.
Pageof 4