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

Alexander Pemov

Showing results (1-10 of 21) with videos related to

Pageof 3
Sort By:
Investigative Ophthalmology & Visual Science|June 12, 2009
A quantitative assessment of the burden and distribution of Lisch nodules in adults with neurofibromatosis type 1Sean Boley, Jennifer L Sloan, Alexander Pemov, et al.
BMC Genomics|March 24, 2010
Evidence of perturbations of cell cycle and DNA repair pathways as a consequence of human and murine NF1-haploinsufficiencyAlexander Pemov, Caroline Park, Karlyne M Reilly, et al.
The Journal of Biological Chemistry|November 28, 2001
A potential role for mini-chromosome maintenance (MCM) proteins in initiation at the dihydrofolate reductase replication originMark G Alexandrow, Marion Ritzi, Alexander Pemov, et al.
Neuro-Oncology Advances|July 10, 2020
Genetics of human malignant peripheral nerve sheath tumorsAlexander Pemov, Hua Li, William Presley, et al.
Genes, Chromosomes & Cancer|January 18, 2012
Mitotic recombination of chromosome arm 17q as a cause of loss of heterozygosity of NF1 in neurofibromatosis type 1-associated glomus tumorsDouglas R Stewart, Alexander Pemov, Peter Van Loo, et al.
Blood Neoplasia|July 22, 2024
The landscape of rare genetic variants in familial Waldenström macroglobulinemiaAlexander Pemov, Jung Kim, Wen Luo, et al.
Molecular Genetics & Genomic Medicine|September 2, 2020
Genome-wide association study of café-au-lait macule number in neurofibromatosis type 1Heejong Sung, Paula L Hyland, Alexander Pemov, et al.
Scientific Reports|July 30, 2020
Comparative clinical and genomic analysis of neurofibromatosis type 2-associated cranial and spinal meningiomasAlexander Pemov, Ramita Dewan, Nancy F Hansen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 1, 2020
A molecular basis for neurofibroma-associated skeletal manifestations in NF1Yun Ma, Andrea M Gross, Eva Dombi, et al.
Plos One|June 4, 2014
Dubowitz syndrome is a complex comprised of multiple, genetically distinct and phenotypically overlapping disordersDouglas R Stewart, Alexander Pemov, Jennifer J Johnston, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Investigative Ophthalmology & Visual Science|June 12, 2009
A quantitative assessment of the burden and distribution of Lisch nodules in adults with neurofibromatosis type 1Sean Boley, Jennifer L Sloan, Alexander Pemov, et al.
BMC Genomics|March 24, 2010
Evidence of perturbations of cell cycle and DNA repair pathways as a consequence of human and murine NF1-haploinsufficiencyAlexander Pemov, Caroline Park, Karlyne M Reilly, et al.
The Journal of Biological Chemistry|November 28, 2001
A potential role for mini-chromosome maintenance (MCM) proteins in initiation at the dihydrofolate reductase replication originMark G Alexandrow, Marion Ritzi, Alexander Pemov, et al.
Neuro-Oncology Advances|July 10, 2020
Genetics of human malignant peripheral nerve sheath tumorsAlexander Pemov, Hua Li, William Presley, et al.
Genes, Chromosomes & Cancer|January 18, 2012
Mitotic recombination of chromosome arm 17q as a cause of loss of heterozygosity of NF1 in neurofibromatosis type 1-associated glomus tumorsDouglas R Stewart, Alexander Pemov, Peter Van Loo, et al.
Blood Neoplasia|July 22, 2024
The landscape of rare genetic variants in familial Waldenström macroglobulinemiaAlexander Pemov, Jung Kim, Wen Luo, et al.
Molecular Genetics & Genomic Medicine|September 2, 2020
Genome-wide association study of café-au-lait macule number in neurofibromatosis type 1Heejong Sung, Paula L Hyland, Alexander Pemov, et al.
Scientific Reports|July 30, 2020
Comparative clinical and genomic analysis of neurofibromatosis type 2-associated cranial and spinal meningiomasAlexander Pemov, Ramita Dewan, Nancy F Hansen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 1, 2020
A molecular basis for neurofibroma-associated skeletal manifestations in NF1Yun Ma, Andrea M Gross, Eva Dombi, et al.
Plos One|June 4, 2014
Dubowitz syndrome is a complex comprised of multiple, genetically distinct and phenotypically overlapping disordersDouglas R Stewart, Alexander Pemov, Jennifer J Johnston, et al.
Pageof 3