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L Pucci

Showing results (61-70 of 70) with videos related to

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American Journal of Human Genetics|July 1, 1997
Inter- and intrachromosomal rearrangements are both involved in the origin of 15q11-q13 deletions in Prader-Willi syndromeR Carrozzo, E Rossi, S L Christian, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 10, 2004
Lack of evidence for the 1484insG variant at the 3'-UTR of the protein tyrosine phosphatase 1B (PTP1B) gene as a genetic determinant of diabetic nephropathy development in type 1 diabetic patientsS De Cosmo, A Marucci, E Ciociola, et al.
The International Journal of Tuberculosis and Lung Disease : the Official Journal of the International Union Against Tuberculosis and Lung Disease|October 26, 2016
Blood and urine inducible protein 10 as potential markers of disease activityL Petrone, A Cannas, V Vanini, et al.
Diabetologia|June 21, 2007
Glucose tolerance is negatively associated with circulating progenitor cell levelsG P Fadini, L Pucci, R Vanacore, et al.
Transplantation Proceedings|January 1, 1998
Sperm-mediated gene transfer: production of pigs transgenic for a human regulator of complement activationM Lavitrano, M Forni, V Varzi, et al.
Dermatologic Surgery : Official Publication for American Society for Dermatologic Surgery [Et Al.]|April 30, 2016
A Comprehensive Approach to Multimodal Facial Aesthetic Treatment: Injection Techniques and Treatment Characteristics From the HARMONY StudyVic A Narurkar, Joel L Cohen, Steven Dayan, et al.
Current Cancer Drug Targets|June 29, 2010
Concomitant CXCR4 and CXCR7 expression predicts poor prognosis in renal cancerC D'Alterio, C Consales, M Polimeno, et al.
Transplantation Proceedings|March 20, 1999
Human decay accelerating factor transgenic pigs for xenotransplantation obtained by sperm-mediated gene transferM Lavitrano, A Stoppacciaro, M L Bacci, et al.
American Journal of Medical Genetics. Part A|December 21, 2002
18q-syndrome and ectodermal dysplasia syndrome: description of a child and his familyR Zannolli, M Pierluigi, L Pucci, et al.
Journal of Medical Genetics|November 25, 2003
Hereditary xanthinuria type II associated with mental delay, autism, cortical renal cysts, nephrocalcinosis, osteopenia, and hair and teeth defectsR Zannolli, V Micheli, M A Mazzei, et al.
Pageof 7

Showing results (61-70 of 70) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 70 results.
American Journal of Human Genetics|July 1, 1997
Inter- and intrachromosomal rearrangements are both involved in the origin of 15q11-q13 deletions in Prader-Willi syndromeR Carrozzo, E Rossi, S L Christian, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 10, 2004
Lack of evidence for the 1484insG variant at the 3'-UTR of the protein tyrosine phosphatase 1B (PTP1B) gene as a genetic determinant of diabetic nephropathy development in type 1 diabetic patientsS De Cosmo, A Marucci, E Ciociola, et al.
The International Journal of Tuberculosis and Lung Disease : the Official Journal of the International Union Against Tuberculosis and Lung Disease|October 26, 2016
Blood and urine inducible protein 10 as potential markers of disease activityL Petrone, A Cannas, V Vanini, et al.
Diabetologia|June 21, 2007
Glucose tolerance is negatively associated with circulating progenitor cell levelsG P Fadini, L Pucci, R Vanacore, et al.
Transplantation Proceedings|January 1, 1998
Sperm-mediated gene transfer: production of pigs transgenic for a human regulator of complement activationM Lavitrano, M Forni, V Varzi, et al.
Dermatologic Surgery : Official Publication for American Society for Dermatologic Surgery [Et Al.]|April 30, 2016
A Comprehensive Approach to Multimodal Facial Aesthetic Treatment: Injection Techniques and Treatment Characteristics From the HARMONY StudyVic A Narurkar, Joel L Cohen, Steven Dayan, et al.
Current Cancer Drug Targets|June 29, 2010
Concomitant CXCR4 and CXCR7 expression predicts poor prognosis in renal cancerC D'Alterio, C Consales, M Polimeno, et al.
Transplantation Proceedings|March 20, 1999
Human decay accelerating factor transgenic pigs for xenotransplantation obtained by sperm-mediated gene transferM Lavitrano, A Stoppacciaro, M L Bacci, et al.
American Journal of Medical Genetics. Part A|December 21, 2002
18q-syndrome and ectodermal dysplasia syndrome: description of a child and his familyR Zannolli, M Pierluigi, L Pucci, et al.
Journal of Medical Genetics|November 25, 2003
Hereditary xanthinuria type II associated with mental delay, autism, cortical renal cysts, nephrocalcinosis, osteopenia, and hair and teeth defectsR Zannolli, V Micheli, M A Mazzei, et al.
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