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

Kristiina Rull

Showing results (31-40 of 42) with videos related to

Pageof 5
Sort By:
The Journal of Clinical Endocrinology and Metabolism|September 11, 2008
Chorionic gonadotropin beta-gene variants are associated with recurrent miscarriage in two European populationsKristiina Rull, Liina Nagirnaja, Veli-Matti Ulander, et al.
Journal of Child Neurology|July 13, 2022
Maternal Pyelonephritis as a Potential Cause of Perinatal Periventricular Venous Infarction in Term-Born ChildrenNorman Ilves, Rael Laugesaar, Kristiina Rull, et al.
Plos One|November 13, 2012
Mid-gestational gene expression profile in placenta and link to pregnancy complicationsLiis Uusküla, Jaana Männik, Kristiina Rull, et al.
Human Reproduction (Oxford, England)|April 5, 2018
FSHB -211 G>T is a major genetic modulator of reproductive physiology and health in childbearing age womenKristiina Rull, Marina Grigorova, Aivar Ehrenberg, et al.
Scientific Reports|August 14, 2015
Extensive shift in placental transcriptome profile in preeclampsia and placental origin of adverse pregnancy outcomesSiim Sõber, Mario Reiman, Triin Kikas, et al.
Scientific Reports|September 1, 2017
The Influence of Different Maternal Microbial Communities on the Development of Infant Gut and Oral MicrobiotaTiina Drell, Jelena Štšepetova, Jaak Simm, et al.
Human Mutation|May 16, 2014
Structural genomic variation as risk factor for idiopathic recurrent miscarriageLiina Nagirnaja, Priit Palta, Laura Kasak, et al.
Molecular Human Reproduction|May 5, 2012
Structural and functional analysis of rare missense mutations in human chorionic gonadotrophin β-subunitLiina Nagirnaja, Česlovas Venclovas, Kristiina Rull, et al.
Elife|March 30, 2021
A common 1.6 mb Y-chromosomal inversion predisposes to subsequent deletions and severe spermatogenic failure in humansPille Hallast, Laura Kibena, Margus Punab, et al.
Epigenetics|December 2, 2014
Using RNA sequencing for identifying gene imprinting and random monoallelic expression in human placentaTauno Metsalu, Triin Viltrop, Airi Tiirats, et al.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
The Journal of Clinical Endocrinology and Metabolism|September 11, 2008
Chorionic gonadotropin beta-gene variants are associated with recurrent miscarriage in two European populationsKristiina Rull, Liina Nagirnaja, Veli-Matti Ulander, et al.
Journal of Child Neurology|July 13, 2022
Maternal Pyelonephritis as a Potential Cause of Perinatal Periventricular Venous Infarction in Term-Born ChildrenNorman Ilves, Rael Laugesaar, Kristiina Rull, et al.
Plos One|November 13, 2012
Mid-gestational gene expression profile in placenta and link to pregnancy complicationsLiis Uusküla, Jaana Männik, Kristiina Rull, et al.
Human Reproduction (Oxford, England)|April 5, 2018
FSHB -211 G>T is a major genetic modulator of reproductive physiology and health in childbearing age womenKristiina Rull, Marina Grigorova, Aivar Ehrenberg, et al.
Scientific Reports|August 14, 2015
Extensive shift in placental transcriptome profile in preeclampsia and placental origin of adverse pregnancy outcomesSiim Sõber, Mario Reiman, Triin Kikas, et al.
Scientific Reports|September 1, 2017
The Influence of Different Maternal Microbial Communities on the Development of Infant Gut and Oral MicrobiotaTiina Drell, Jelena Štšepetova, Jaak Simm, et al.
Human Mutation|May 16, 2014
Structural genomic variation as risk factor for idiopathic recurrent miscarriageLiina Nagirnaja, Priit Palta, Laura Kasak, et al.
Molecular Human Reproduction|May 5, 2012
Structural and functional analysis of rare missense mutations in human chorionic gonadotrophin β-subunitLiina Nagirnaja, Česlovas Venclovas, Kristiina Rull, et al.
Elife|March 30, 2021
A common 1.6 mb Y-chromosomal inversion predisposes to subsequent deletions and severe spermatogenic failure in humansPille Hallast, Laura Kibena, Margus Punab, et al.
Epigenetics|December 2, 2014
Using RNA sequencing for identifying gene imprinting and random monoallelic expression in human placentaTauno Metsalu, Triin Viltrop, Airi Tiirats, et al.
Pageof 5