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

K M Allen

Showing results (41-50 of 52) with videos related to

Pageof 6
Sort By:
The American Review of Respiratory Disease|July 1, 1990
Estimation of the probability of disturbed breathing during sleep before a sleep studyB D Crocker, L G Olson, N A Saunders, et al.
British Journal of Obstetrics and Gynaecology|January 1, 1984
The symptomatology of the climacteric in relation to hormonal and cytological factorsC E James, A J Breeson, G Kovacs, et al.
Journal of Neurology|February 1, 2000
Studies of the candidate genes in X-linked congenital cerebellar hypoplasiaS N Illarioshkin, K M Allen, J G Gleeson, et al.
Nature Genetics|September 10, 1998
PAK3 mutation in nonsyndromic X-linked mental retardationK M Allen, J G Gleeson, S Bagrodia, et al.
Journal of Medicinal Chemistry|March 1, 1983
Synthesis and biological activity of zoapatanol analoguesM C Wani, B R Vishnuvajjala, W E Swain, et al.
Molecular Psychiatry|July 15, 2015
Association of serum VEGF levels with prefrontal cortex volume in schizophreniaA Pillai, K R Howell, A O Ahmed, et al.
Human Molecular Genetics|November 18, 1998
LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformationD T Pilz, N Matsumoto, S Minnerath, et al.
Bone|June 23, 2004
Bone biomechanical properties in LRP5 mutant miceM P Akhter, D J Wells, S J Short, et al.
Cell|March 7, 1998
Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling proteinJ G Gleeson, K M Allen, J W Fox, et al.
Molecular Psychiatry|October 17, 2012
Molecular evidence of N-methyl-D-aspartate receptor hypofunction in schizophreniaC S Weickert, S J Fung, V S Catts, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
The American Review of Respiratory Disease|July 1, 1990
Estimation of the probability of disturbed breathing during sleep before a sleep studyB D Crocker, L G Olson, N A Saunders, et al.
British Journal of Obstetrics and Gynaecology|January 1, 1984
The symptomatology of the climacteric in relation to hormonal and cytological factorsC E James, A J Breeson, G Kovacs, et al.
Journal of Neurology|February 1, 2000
Studies of the candidate genes in X-linked congenital cerebellar hypoplasiaS N Illarioshkin, K M Allen, J G Gleeson, et al.
Nature Genetics|September 10, 1998
PAK3 mutation in nonsyndromic X-linked mental retardationK M Allen, J G Gleeson, S Bagrodia, et al.
Journal of Medicinal Chemistry|March 1, 1983
Synthesis and biological activity of zoapatanol analoguesM C Wani, B R Vishnuvajjala, W E Swain, et al.
Molecular Psychiatry|July 15, 2015
Association of serum VEGF levels with prefrontal cortex volume in schizophreniaA Pillai, K R Howell, A O Ahmed, et al.
Human Molecular Genetics|November 18, 1998
LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformationD T Pilz, N Matsumoto, S Minnerath, et al.
Bone|June 23, 2004
Bone biomechanical properties in LRP5 mutant miceM P Akhter, D J Wells, S J Short, et al.
Cell|March 7, 1998
Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling proteinJ G Gleeson, K M Allen, J W Fox, et al.
Molecular Psychiatry|October 17, 2012
Molecular evidence of N-methyl-D-aspartate receptor hypofunction in schizophreniaC S Weickert, S J Fung, V S Catts, et al.
Pageof 6