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L Ruiz

Showing results (811-820 of 908) with videos related to

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Human Mutation|June 13, 2012
Mutations in PLOD2 cause autosomal-recessive connective tissue disorders within the Bruck syndrome--osteogenesis imperfecta phenotypic spectrumMaria Trinidad Puig-Hervás, Samia Temtamy, Mona Aglan, et al.
AIDS Research and Human Retroviruses|April 25, 2000
Baseline HIV type 1 genotypic resistance to a newly added nucleoside analog is predictive of virologic failure of the new therapyK Van Vaerenbergh, K Van Laethem, E Van Wijngaerden, et al.
Microorganisms|December 22, 2019
Identification of Insect-Deterrent Metabolites from <i>Acremonium masseei</i> strain CICY026, a Saprophytic Fungus from a Sinkhole in YucatánAna L Ruiz-Jiménez, Esaú Ruiz-Sánchez, Gabriela Heredia, et al.
American Journal of Medical Genetics. Part A|April 28, 2015
Identification of a premature stop codon mutation in the PHGDH gene in severe Neu-Laxova syndrome-evidence for phenotypic variabilityEduardo P Mattos, André Anjos da Silva, José Antônio A Magalhães, et al.
American Journal of Medical Genetics. Part A|October 29, 2022
A large, ten-generation family with autosomal dominant preaxial polydactyly/triphalangeal thumb: Historical, clinical, genealogical, and molecular studiesLuis Francisco González Álvarez, Jair Tenorio-Castaño, Fernando A Poletta, et al.
The Review of Scientific Instruments|December 3, 2008
One-dimensional neutron imager for the Sandia Z facilityDavid N Fittinghoff, Dan E Bower, James R Hollaway, et al.
Human Mutation|October 8, 2009
Widening the mutation spectrum of EVC and EVC2: ectopic expression of Weyer variants in NIH 3T3 fibroblasts disrupts Hedgehog signalingMaria Valencia, Pablo Lapunzina, Derek Lim, et al.
Cancer Epidemiology|July 9, 2016
Perinatal and childhood factors and risk of prostate cancer in adulthood: MCC-Spain case-control studyVirginia Lope, Esther García-Esquinas, José Manuel Ruiz-Dominguez, et al.
Human Molecular Genetics|October 4, 2017
GLI1 inactivation is associated with developmental phenotypes overlapping with Ellis-van Creveld syndromeAdrian Palencia-Campos, Asmat Ullah, Julian Nevado, et al.
Physical Review Letters|August 23, 2002
X-ray imaging measurements of capsule implosions driven by a Z-pinch dynamic hohlraumJ E Bailey, G A Chandler, S A Slutz, et al.
Pageof 91

Showing results (811-820 of 908) with videos related to

Sort By:
Pageof 91
Human Mutation|June 13, 2012
Mutations in PLOD2 cause autosomal-recessive connective tissue disorders within the Bruck syndrome--osteogenesis imperfecta phenotypic spectrumMaria Trinidad Puig-Hervás, Samia Temtamy, Mona Aglan, et al.
AIDS Research and Human Retroviruses|April 25, 2000
Baseline HIV type 1 genotypic resistance to a newly added nucleoside analog is predictive of virologic failure of the new therapyK Van Vaerenbergh, K Van Laethem, E Van Wijngaerden, et al.
Microorganisms|December 22, 2019
Identification of Insect-Deterrent Metabolites from <i>Acremonium masseei</i> strain CICY026, a Saprophytic Fungus from a Sinkhole in YucatánAna L Ruiz-Jiménez, Esaú Ruiz-Sánchez, Gabriela Heredia, et al.
American Journal of Medical Genetics. Part A|April 28, 2015
Identification of a premature stop codon mutation in the PHGDH gene in severe Neu-Laxova syndrome-evidence for phenotypic variabilityEduardo P Mattos, André Anjos da Silva, José Antônio A Magalhães, et al.
American Journal of Medical Genetics. Part A|October 29, 2022
A large, ten-generation family with autosomal dominant preaxial polydactyly/triphalangeal thumb: Historical, clinical, genealogical, and molecular studiesLuis Francisco González Álvarez, Jair Tenorio-Castaño, Fernando A Poletta, et al.
The Review of Scientific Instruments|December 3, 2008
One-dimensional neutron imager for the Sandia Z facilityDavid N Fittinghoff, Dan E Bower, James R Hollaway, et al.
Human Mutation|October 8, 2009
Widening the mutation spectrum of EVC and EVC2: ectopic expression of Weyer variants in NIH 3T3 fibroblasts disrupts Hedgehog signalingMaria Valencia, Pablo Lapunzina, Derek Lim, et al.
Cancer Epidemiology|July 9, 2016
Perinatal and childhood factors and risk of prostate cancer in adulthood: MCC-Spain case-control studyVirginia Lope, Esther García-Esquinas, José Manuel Ruiz-Dominguez, et al.
Human Molecular Genetics|October 4, 2017
GLI1 inactivation is associated with developmental phenotypes overlapping with Ellis-van Creveld syndromeAdrian Palencia-Campos, Asmat Ullah, Julian Nevado, et al.
Physical Review Letters|August 23, 2002
X-ray imaging measurements of capsule implosions driven by a Z-pinch dynamic hohlraumJ E Bailey, G A Chandler, S A Slutz, et al.
Pageof 91