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

Rachel A Burt

Showing results (11-20 of 24) with videos related to

Pageof 3
Sort By:
Scientific Reports|April 5, 2018
An intronic mutation in Chd7 creates a cryptic splice site, causing aberrant splicing in a mouse model of CHARGE syndromeJacqueline M Ogier, Benedicta D Arhatari, Marina R Carpinelli, et al.
Nature Genetics|June 9, 2004
Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophreniaJun Mukai, Hui Liu, Rachel A Burt, et al.
Plos One|May 21, 2014
CHD7 deficiency in "Looper", a new mouse model of CHARGE syndrome, results in ossicle malformation, otosclerosis and hearing impairmentJacqueline M Ogier, Marina R Carpinelli, Benedicta D Arhatari, et al.
Disease Models & Mechanisms|April 1, 2014
A new mouse model of Canavan leukodystrophy displays hearing impairment due to central nervous system dysmyelinationMarina R Carpinelli, Anne K Voss, Michael G Manning, et al.
Infection and Immunity|July 16, 2002
Mice that are congenic for the char2 locus are susceptible to malariaRachel A Burt, Vikki M Marshall, Jamie Wagglen, et al.
The American Journal of Pathology|June 22, 2015
Mice Haploinsufficient for Ets1 and Fli1 Display Middle Ear Abnormalities and Model Aspects of Jacobsen SyndromeMarina R Carpinelli, Elizabeth A Kruse, Benedicta D Arhatari, et al.
Archives of Disease in Childhood|February 2, 2018
Cross-sectional epidemiology of hearing loss in Australian children aged 11-12 years old and 25-year secular trendsJing Wang, Carlijn M P le Clercq, Valerie Sung, et al.
Developmental Biology|January 20, 2025
Loss of KAT6B causes premature ossification and promotes osteoblast differentiation during developmentMaria I Bergamasco, Jacqueline M Ogier, Alexandra L Garnham, et al.
American Journal of Human Genetics|January 30, 2004
Genomewide scan in families with schizophrenia from the founder population of Afrikaners reveals evidence for linkage and uniparental disomy on chromosome 1Gonçalo R Abecasis, Rachel A Burt, Diana Hall, et al.
Journal of Immunology (Baltimore, Md. : 1950)|December 17, 2009
An NZW-derived interval on chromosome 7 moderates sialadenitis, but not insulitis in congenic nonobese diabetic miceRachel A Burt, Laura Watkins, Iris K L Tan, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Scientific Reports|April 5, 2018
An intronic mutation in Chd7 creates a cryptic splice site, causing aberrant splicing in a mouse model of CHARGE syndromeJacqueline M Ogier, Benedicta D Arhatari, Marina R Carpinelli, et al.
Nature Genetics|June 9, 2004
Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophreniaJun Mukai, Hui Liu, Rachel A Burt, et al.
Plos One|May 21, 2014
CHD7 deficiency in "Looper", a new mouse model of CHARGE syndrome, results in ossicle malformation, otosclerosis and hearing impairmentJacqueline M Ogier, Marina R Carpinelli, Benedicta D Arhatari, et al.
Disease Models & Mechanisms|April 1, 2014
A new mouse model of Canavan leukodystrophy displays hearing impairment due to central nervous system dysmyelinationMarina R Carpinelli, Anne K Voss, Michael G Manning, et al.
Infection and Immunity|July 16, 2002
Mice that are congenic for the char2 locus are susceptible to malariaRachel A Burt, Vikki M Marshall, Jamie Wagglen, et al.
The American Journal of Pathology|June 22, 2015
Mice Haploinsufficient for Ets1 and Fli1 Display Middle Ear Abnormalities and Model Aspects of Jacobsen SyndromeMarina R Carpinelli, Elizabeth A Kruse, Benedicta D Arhatari, et al.
Archives of Disease in Childhood|February 2, 2018
Cross-sectional epidemiology of hearing loss in Australian children aged 11-12 years old and 25-year secular trendsJing Wang, Carlijn M P le Clercq, Valerie Sung, et al.
Developmental Biology|January 20, 2025
Loss of KAT6B causes premature ossification and promotes osteoblast differentiation during developmentMaria I Bergamasco, Jacqueline M Ogier, Alexandra L Garnham, et al.
American Journal of Human Genetics|January 30, 2004
Genomewide scan in families with schizophrenia from the founder population of Afrikaners reveals evidence for linkage and uniparental disomy on chromosome 1Gonçalo R Abecasis, Rachel A Burt, Diana Hall, et al.
Journal of Immunology (Baltimore, Md. : 1950)|December 17, 2009
An NZW-derived interval on chromosome 7 moderates sialadenitis, but not insulitis in congenic nonobese diabetic miceRachel A Burt, Laura Watkins, Iris K L Tan, et al.
Pageof 3