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

E Botta

Showing results (31-40 of 106) with videos related to

Pageof 11
Sort By:
American Journal of Human Genetics|January 1, 1995
Molecular and cellular analysis of the DNA repair defect in a patient in xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and Cockayne syndromeB C Broughton, A F Thompson, S A Harcourt, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 5, 1997
Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription geneE M Taylor, B C Broughton, E Botta, et al.
The Journal of Investigative Dermatology|October 1, 1996
DNA repair and ultraviolet mutagenesis in cells from a new patient with xeroderma pigmentosum group G and cockayne syndrome resemble xeroderma pigmentosum cellsS Moriwaki, M Stefanini, A R Lehmann, et al.
Annals of Hematology|April 16, 2018
- 174 G>C IL-6 polymorphism and primary iron overload in male patientsWalter F Tetzlaff, Tomás Meroño, Eliana E Botta, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|December 13, 2021
Vascular inflammation and impaired reverse cholesterol transport and lipid metabolism in obese children and adolescentsMaximiliano Martin, Laura Gaete, Walter Tetzlaff, et al.
Mutation Research|August 8, 1996
A CHO mutant, UV40, that is sensitive to diverse mutagens and represents a new complementation group of mitomycin C sensitivityD B Busch, M Z Zdzienicka, A T Natarajan, et al.
Transplantation Proceedings|August 19, 2014
Short- and long-term outcomes of every graft recovered during a multi-organ procurement procedure including the intestineP A Farinelli, J M Padin, J C Troncoso, et al.
Physical Review Letters|March 10, 2012
Evidence for heavy hyperhydrogen (Λ)(6)hM Agnello, L Benussi, M Bertani, et al.
Physical Review Letters|August 11, 2005
Evidence for a kaon-bound state K(-)pp produced in K(-) absorption reactions at restM Agnello, G Beer, L Benussi, et al.
Physical Review Letters|December 10, 2015
Observation of Spin-Dependent Charge Symmetry Breaking in ΛN Interaction: Gamma-Ray Spectroscopy of _{Λ}^{4}HeT O Yamamoto, M Agnello, Y Akazawa, et al.
Pageof 11

Showing results (31-40 of 106) with videos related to

Sort By:
Pageof 11
American Journal of Human Genetics|January 1, 1995
Molecular and cellular analysis of the DNA repair defect in a patient in xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and Cockayne syndromeB C Broughton, A F Thompson, S A Harcourt, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 5, 1997
Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription geneE M Taylor, B C Broughton, E Botta, et al.
The Journal of Investigative Dermatology|October 1, 1996
DNA repair and ultraviolet mutagenesis in cells from a new patient with xeroderma pigmentosum group G and cockayne syndrome resemble xeroderma pigmentosum cellsS Moriwaki, M Stefanini, A R Lehmann, et al.
Annals of Hematology|April 16, 2018
- 174 G>C IL-6 polymorphism and primary iron overload in male patientsWalter F Tetzlaff, Tomás Meroño, Eliana E Botta, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|December 13, 2021
Vascular inflammation and impaired reverse cholesterol transport and lipid metabolism in obese children and adolescentsMaximiliano Martin, Laura Gaete, Walter Tetzlaff, et al.
Mutation Research|August 8, 1996
A CHO mutant, UV40, that is sensitive to diverse mutagens and represents a new complementation group of mitomycin C sensitivityD B Busch, M Z Zdzienicka, A T Natarajan, et al.
Transplantation Proceedings|August 19, 2014
Short- and long-term outcomes of every graft recovered during a multi-organ procurement procedure including the intestineP A Farinelli, J M Padin, J C Troncoso, et al.
Physical Review Letters|March 10, 2012
Evidence for heavy hyperhydrogen (Λ)(6)hM Agnello, L Benussi, M Bertani, et al.
Physical Review Letters|August 11, 2005
Evidence for a kaon-bound state K(-)pp produced in K(-) absorption reactions at restM Agnello, G Beer, L Benussi, et al.
Physical Review Letters|December 10, 2015
Observation of Spin-Dependent Charge Symmetry Breaking in ΛN Interaction: Gamma-Ray Spectroscopy of _{Λ}^{4}HeT O Yamamoto, M Agnello, Y Akazawa, et al.
Pageof 11