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D Padilla

Showing results (121-130 of 148) with videos related to

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Molecular and Cellular Endocrinology|December 23, 2008
HSD17B4 overexpression, an independent biomarker of poor patient outcome in prostate cancerKrishan K Rasiah, Margaret Gardiner-Garden, Emma J D Padilla, et al.
BJU International|November 8, 2007
The rs743572 common variant in the promoter of CYP17A1 is not associated with prostate cancer risk or circulating hormonal levelsGianluca Severi, Vanessa M Hayes, Andrea A Tesoriero, et al.
Nature Genetics|January 4, 2001
Dominant effector genetics in mammalian cellsX Xu, C Leo, Y Jang, et al.
International Journal of Neonatal Screening|December 16, 2020
Philippine Performance Evaluation and Assessment Scheme (PPEAS): Experiences in Newborn Screening System Quality ImprovementCarmencita D Padilla, Bradford L Therrell, Karen Asuncion R Panol, et al.
Revista Espanola De Quimioterapia : Publicacion Oficial De La Sociedad Espanola De Quimioterapia|December 5, 2019
[Development of animal experimental model for bacterial peritonitis]O Montenegro, S Illescas, J C González, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|June 16, 2006
Variants in the prostate-specific antigen (PSA) gene and prostate cancer risk, survival, and circulating PSAGianluca Severi, Vanessa M Hayes, Petra Neufing, et al.
Molecular Genetics and Metabolism|June 10, 2018
Universal newborn screening: A roadmap for actionC P Howson, B Cedergren, R Giugliani, et al.
Molecular Genetics and Metabolism|June 25, 2019
Corrigendum to Universal newborn screening: A roadmap for action molecular genetics and metabolism 124 (2018) 177-183C P Howson, B Cedergren, R Giugliani, et al.
Medrxiv : the Preprint Server for Health Sciences|January 8, 2026
Laterality and Completeness Patterns of Nonsyndromic Clefts in a Multiethnic CohortChristina Spencer, Ligiane A Machado-Paula, Fang Qian, et al.
Orphanet Journal of Rare Diseases|September 11, 2024
Operational description of rare diseases: a reference to improve the recognition and visibility of rare diseasesChiuhui Mary Wang, Amy Heagle Whiting, Ana Rath, et al.
Pageof 15

Showing results (121-130 of 148) with videos related to

Sort By:
Pageof 15
Molecular and Cellular Endocrinology|December 23, 2008
HSD17B4 overexpression, an independent biomarker of poor patient outcome in prostate cancerKrishan K Rasiah, Margaret Gardiner-Garden, Emma J D Padilla, et al.
BJU International|November 8, 2007
The rs743572 common variant in the promoter of CYP17A1 is not associated with prostate cancer risk or circulating hormonal levelsGianluca Severi, Vanessa M Hayes, Andrea A Tesoriero, et al.
Nature Genetics|January 4, 2001
Dominant effector genetics in mammalian cellsX Xu, C Leo, Y Jang, et al.
International Journal of Neonatal Screening|December 16, 2020
Philippine Performance Evaluation and Assessment Scheme (PPEAS): Experiences in Newborn Screening System Quality ImprovementCarmencita D Padilla, Bradford L Therrell, Karen Asuncion R Panol, et al.
Revista Espanola De Quimioterapia : Publicacion Oficial De La Sociedad Espanola De Quimioterapia|December 5, 2019
[Development of animal experimental model for bacterial peritonitis]O Montenegro, S Illescas, J C González, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|June 16, 2006
Variants in the prostate-specific antigen (PSA) gene and prostate cancer risk, survival, and circulating PSAGianluca Severi, Vanessa M Hayes, Petra Neufing, et al.
Molecular Genetics and Metabolism|June 10, 2018
Universal newborn screening: A roadmap for actionC P Howson, B Cedergren, R Giugliani, et al.
Molecular Genetics and Metabolism|June 25, 2019
Corrigendum to Universal newborn screening: A roadmap for action molecular genetics and metabolism 124 (2018) 177-183C P Howson, B Cedergren, R Giugliani, et al.
Medrxiv : the Preprint Server for Health Sciences|January 8, 2026
Laterality and Completeness Patterns of Nonsyndromic Clefts in a Multiethnic CohortChristina Spencer, Ligiane A Machado-Paula, Fang Qian, et al.
Orphanet Journal of Rare Diseases|September 11, 2024
Operational description of rare diseases: a reference to improve the recognition and visibility of rare diseasesChiuhui Mary Wang, Amy Heagle Whiting, Ana Rath, et al.
Pageof 15