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

H Wallace

Showing results (341-350 of 365) with videos related to

Pageof 37
Sort By:
Experimental Cell Research|December 8, 2007
Mutationally activated K-ras 4A and 4B both mediate lung carcinogenesisCharles E Patek, Mark J Arends, William A H Wallace, et al.
Journal of Medicinal Chemistry|October 1, 2004
Rationale, design, and synthesis of novel phenyl imidazoles as opioid receptor agonists for gastrointestinal disordersHenry J Breslin, Tamara A Miskowski, Bryan M Rafferty, et al.
Neurology|September 25, 2003
Sodium channel alpha1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasmsR H Wallace, B L Hodgson, B E Grinton, et al.
Bioorganic & Medicinal Chemistry|August 23, 2005
Aza-bicyclic amino acid carboxamides as alpha4beta1/alpha4beta7 integrin receptor antagonistsAlexey B Dyatkin, Yong Gong, Tamara A Miskowski, et al.
Brain : a Journal of Neurology|October 6, 2006
Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutationsIngrid E Scheffer, Louise A Harkin, Bronwyn E Grinton, et al.
Epilepsia|August 27, 2004
Familial partial epilepsy with variable foci: clinical features and linkage to chromosome 22q12Samuel F Berkovic, Jose M Serratosa, Hilary A Phillips, et al.
Human Reproduction (Oxford, England)|May 25, 2024
The impact of treatment for childhood classical Hodgkin lymphoma according to the EuroNet-PHL-C2 protocol on serum anti-Müllerian HormoneK C E Drechsel, S L Broer, F S Stoutjesdijk, et al.
Nature Genetics|March 13, 2002
Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsyPetter Strømme, Marie E Mangelsdorf, Marie A Shaw, et al.
American Journal of Human Genetics|March 20, 2001
Neuronal sodium-channel alpha1-subunit mutations in generalized epilepsy with febrile seizures plusR H Wallace, I E Scheffer, S Barnett, et al.
American Journal of Respiratory and Critical Care Medicine|July 24, 2012
Monocytes control second-phase neutrophil emigration in established lipopolysaccharide-induced murine lung injuryKevin Dhaliwal, Emma Scholefield, David Ferenbach, et al.
Pageof 37

Showing results (341-350 of 365) with videos related to

Sort By:
Pageof 37
Experimental Cell Research|December 8, 2007
Mutationally activated K-ras 4A and 4B both mediate lung carcinogenesisCharles E Patek, Mark J Arends, William A H Wallace, et al.
Journal of Medicinal Chemistry|October 1, 2004
Rationale, design, and synthesis of novel phenyl imidazoles as opioid receptor agonists for gastrointestinal disordersHenry J Breslin, Tamara A Miskowski, Bryan M Rafferty, et al.
Neurology|September 25, 2003
Sodium channel alpha1-subunit mutations in severe myoclonic epilepsy of infancy and infantile spasmsR H Wallace, B L Hodgson, B E Grinton, et al.
Bioorganic & Medicinal Chemistry|August 23, 2005
Aza-bicyclic amino acid carboxamides as alpha4beta1/alpha4beta7 integrin receptor antagonistsAlexey B Dyatkin, Yong Gong, Tamara A Miskowski, et al.
Brain : a Journal of Neurology|October 6, 2006
Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutationsIngrid E Scheffer, Louise A Harkin, Bronwyn E Grinton, et al.
Epilepsia|August 27, 2004
Familial partial epilepsy with variable foci: clinical features and linkage to chromosome 22q12Samuel F Berkovic, Jose M Serratosa, Hilary A Phillips, et al.
Human Reproduction (Oxford, England)|May 25, 2024
The impact of treatment for childhood classical Hodgkin lymphoma according to the EuroNet-PHL-C2 protocol on serum anti-Müllerian HormoneK C E Drechsel, S L Broer, F S Stoutjesdijk, et al.
Nature Genetics|March 13, 2002
Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsyPetter Strømme, Marie E Mangelsdorf, Marie A Shaw, et al.
American Journal of Human Genetics|March 20, 2001
Neuronal sodium-channel alpha1-subunit mutations in generalized epilepsy with febrile seizures plusR H Wallace, I E Scheffer, S Barnett, et al.
American Journal of Respiratory and Critical Care Medicine|July 24, 2012
Monocytes control second-phase neutrophil emigration in established lipopolysaccharide-induced murine lung injuryKevin Dhaliwal, Emma Scholefield, David Ferenbach, et al.
Pageof 37