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

Andrew K Salem

Showing results (1-10 of 10) with videos related to

Pageof 1
Sort By:
Thyroid : Official Journal of the American Thyroid Association|June 27, 2008
Effect of sunitinib on growth and function of FRTL-5 thyroid cellsAndrew K Salem, Mike S Fenton, Kenneth M Marion, et al.
Thyroid : Official Journal of the American Thyroid Association|July 16, 2010
Sunitinib inhibits MEK/ERK and SAPK/JNK pathways and increases sodium/iodide symporter expression in papillary thyroid cancerMike S Fenton, Kenneth M Marion, Andrew K Salem, et al.
Cornea|August 28, 2007
Keratoconus is not associated with mutations in COL8A1 and COL8A2Anthony J Aldave, Nirit Bourla, Vivek S Yellore, et al.
Ophthalmic Genetics|June 15, 2007
Autosomal dominant cornea plana is not associated with pathogenic mutations in DCN, DSPG3, FOXC1, KERA, LUM, or PITX2Anthony J Aldave, Baris Sonmez, Nirit Bourla, et al.
Investigative Ophthalmology & Visual Science|August 29, 2006
No pathogenic mutations identified in the COL8A1 and COL8A2 genes in familial Fuchs corneal dystrophyAnthony J Aldave, Sylvia A Rayner, Andrew K Salem, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 12, 2008
A novel variant of combined granular-lattice corneal dystrophy associated with the Met619Lys mutation in the TGFBI geneAnthony J Aldave, Vivek S Yellore, Baris Sonmez, et al.
Cornea|August 2, 2007
Autosomal recessive CHED associated with novel compound heterozygous mutations in SLC4A11Anthony J Aldave, Vivek S Yellore, Nirit Bourla, et al.
Investigative Ophthalmology & Visual Science|June 27, 2006
No VSX1 gene mutations associated with keratoconusAnthony J Aldave, Vivek S Yellore, Andrew K Salem, et al.
American Journal of Medical Genetics. Part A|October 16, 2007
Posterior polymorphous corneal dystrophy is associated with TCF8 gene mutations and abdominal herniaAnthony J Aldave, Vivek S Yellore, Fei Yu, et al.
Cornea|May 4, 2006
No pathogenic mutations identified in the TGFBI gene in polymorphic corneal amyloid depositionAnthony J Aldave, Sylvia A Rayner, Julie A King, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Thyroid : Official Journal of the American Thyroid Association|June 27, 2008
Effect of sunitinib on growth and function of FRTL-5 thyroid cellsAndrew K Salem, Mike S Fenton, Kenneth M Marion, et al.
Thyroid : Official Journal of the American Thyroid Association|July 16, 2010
Sunitinib inhibits MEK/ERK and SAPK/JNK pathways and increases sodium/iodide symporter expression in papillary thyroid cancerMike S Fenton, Kenneth M Marion, Andrew K Salem, et al.
Cornea|August 28, 2007
Keratoconus is not associated with mutations in COL8A1 and COL8A2Anthony J Aldave, Nirit Bourla, Vivek S Yellore, et al.
Ophthalmic Genetics|June 15, 2007
Autosomal dominant cornea plana is not associated with pathogenic mutations in DCN, DSPG3, FOXC1, KERA, LUM, or PITX2Anthony J Aldave, Baris Sonmez, Nirit Bourla, et al.
Investigative Ophthalmology & Visual Science|August 29, 2006
No pathogenic mutations identified in the COL8A1 and COL8A2 genes in familial Fuchs corneal dystrophyAnthony J Aldave, Sylvia A Rayner, Andrew K Salem, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 12, 2008
A novel variant of combined granular-lattice corneal dystrophy associated with the Met619Lys mutation in the TGFBI geneAnthony J Aldave, Vivek S Yellore, Baris Sonmez, et al.
Cornea|August 2, 2007
Autosomal recessive CHED associated with novel compound heterozygous mutations in SLC4A11Anthony J Aldave, Vivek S Yellore, Nirit Bourla, et al.
Investigative Ophthalmology & Visual Science|June 27, 2006
No VSX1 gene mutations associated with keratoconusAnthony J Aldave, Vivek S Yellore, Andrew K Salem, et al.
American Journal of Medical Genetics. Part A|October 16, 2007
Posterior polymorphous corneal dystrophy is associated with TCF8 gene mutations and abdominal herniaAnthony J Aldave, Vivek S Yellore, Fei Yu, et al.
Cornea|May 4, 2006
No pathogenic mutations identified in the TGFBI gene in polymorphic corneal amyloid depositionAnthony J Aldave, Sylvia A Rayner, Julie A King, et al.
Pageof 1