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

P Gasparini

Showing results (161-170 of 204) with videos related to

Pageof 21
Sort By:
European Journal of Human Genetics : EJHG|February 5, 1998
Juvenile and adult hemochromatosis are distinct genetic disordersC Camaschella, A Roetto, M Cicilano, et al.
Human Mutation|July 20, 2001
DHPLC analysis of the MECP2 gene in Italian Rett patientsP Nicolao, M Carella, B Giometto, et al.
European Journal of Human Genetics : EJHG|March 14, 2000
High carrier frequency of the 35delG deafness mutation in European populations. Genetic Analysis Consortium of GJB2 35delGP Gasparini, R Rabionet, G Barbujani, et al.
Oncogene|June 28, 2011
miR-130a targets MET and induces TRAIL-sensitivity in NSCLC by downregulating miR-221 and 222M Acunzo, R Visone, G Romano, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Generation of a transcription map of a 1 Mbase region containing the HFE gene (6p22)A Totaro, A Roetto, J M Rommens, et al.
American Journal of Human Genetics|April 17, 1999
Juvenile hemochromatosis locus maps to chromosome 1qA Roetto, A Totaro, M Cazzola, et al.
BMC Pediatrics|May 11, 2020
Dental anomalies as a possible clue of 1p36 deletion syndrome due to germline mosaicism: a case reportD Nistico', F Guidolin, C O Navarra, et al.
Sports Biomechanics|June 27, 2023
Can gluteal muscle activation discriminate functional performance in moderately trained women? - A cross-sectional studyMarcos S A Souza, Victória M A Valadao, Ana I Teruyu, et al.
Kidney International|March 22, 2001
Cystinuria type I: identification of eight new mutations in SLC3A1L Bisceglia, J Purroy, M Jiménez-Vidal, et al.
American Journal of Human Genetics|August 29, 2001
Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 3T Joensuu, R Hämäläinen, B Yuan, et al.
Pageof 21

Showing results (161-170 of 204) with videos related to

Sort By:
Pageof 21
European Journal of Human Genetics : EJHG|February 5, 1998
Juvenile and adult hemochromatosis are distinct genetic disordersC Camaschella, A Roetto, M Cicilano, et al.
Human Mutation|July 20, 2001
DHPLC analysis of the MECP2 gene in Italian Rett patientsP Nicolao, M Carella, B Giometto, et al.
European Journal of Human Genetics : EJHG|March 14, 2000
High carrier frequency of the 35delG deafness mutation in European populations. Genetic Analysis Consortium of GJB2 35delGP Gasparini, R Rabionet, G Barbujani, et al.
Oncogene|June 28, 2011
miR-130a targets MET and induces TRAIL-sensitivity in NSCLC by downregulating miR-221 and 222M Acunzo, R Visone, G Romano, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Generation of a transcription map of a 1 Mbase region containing the HFE gene (6p22)A Totaro, A Roetto, J M Rommens, et al.
American Journal of Human Genetics|April 17, 1999
Juvenile hemochromatosis locus maps to chromosome 1qA Roetto, A Totaro, M Cazzola, et al.
BMC Pediatrics|May 11, 2020
Dental anomalies as a possible clue of 1p36 deletion syndrome due to germline mosaicism: a case reportD Nistico', F Guidolin, C O Navarra, et al.
Sports Biomechanics|June 27, 2023
Can gluteal muscle activation discriminate functional performance in moderately trained women? - A cross-sectional studyMarcos S A Souza, Victória M A Valadao, Ana I Teruyu, et al.
Kidney International|March 22, 2001
Cystinuria type I: identification of eight new mutations in SLC3A1L Bisceglia, J Purroy, M Jiménez-Vidal, et al.
American Journal of Human Genetics|August 29, 2001
Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 3T Joensuu, R Hämäläinen, B Yuan, et al.
Pageof 21