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S Mancini

Showing results (251-260 of 347) with videos related to

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European Journal of Medical Genetics|November 5, 2018
Mutated zinc finger protein of the cerebellum 1 leads to microcephaly, cortical malformation, callosal agenesis, cerebellar dysplasia, tethered cord and scoliosisLaura V Vandervore, Rachel Schot, A Jeannette M Hoogeboom, et al.
Leukemia Research|July 21, 2018
Erythropoietin levels and erythroid differentiation parameters in patients with lower-risk myelodysplastic syndromesC Gurnari, R Latagliata, F Buccisano, et al.
American Journal of Medical Genetics. Part A|February 16, 2005
Autosomal dominant inheritance of left ventricular outflow tract obstructionMarja W Wessels, Rolf M F Berger, Ingrid M E Frohn-Mulder, et al.
Human Mutation|November 14, 2008
Expanded mutational spectrum in Cohen syndrome, tissue expression, and transcript variants of COH1Wenke Seifert, Muriel Holder-Espinasse, Jirko Kühnisch, et al.
Nature|December 22, 2016
XRCC1 mutation is associated with PARP1 hyperactivation and cerebellar ataxiaNicolas C Hoch, Hana Hanzlikova, Stuart L Rulten, et al.
Clinical Genetics|February 18, 2014
Novel KDM6A (UTX) mutations and a clinical and molecular review of the X-linked Kabuki syndrome (KS2)S Banka, D Lederer, V Benoit, et al.
Journal of Cellular Biochemistry|October 3, 2022
Knockout of NRF2 triggers prostate cancer cells death through ROS modulation and sensitizes to cisplatinMariana C S Mancini, Ana P Morelli, Matheus B Severino, et al.
Environmental Research|November 19, 2023
Multi-target assessment of advanced oxidation processes-based strategies for indirect potable reuse of tertiary wastewater: Fate of compounds of emerging concerns, microbial and ecotoxicological parametersS Murgolo, O De Giglio, C De Ceglie, et al.
European Journal of Human Genetics : EJHG|November 11, 2010
The clinical spectrum of complete FBN1 allele deletionsYvonne Hilhorst-Hofstee, Ben C J Hamel, Joke B G M Verheij, et al.
Journal of Inherited Metabolic Disease|May 11, 2011
Long-term follow-up and treatment in nine boys with X-linked creatine transporter defectJiddeke M van de Kamp, Petra J W Pouwels, Femke K Aarsen, et al.
Pageof 35

Showing results (251-260 of 347) with videos related to

Sort By:
Pageof 35
European Journal of Medical Genetics|November 5, 2018
Mutated zinc finger protein of the cerebellum 1 leads to microcephaly, cortical malformation, callosal agenesis, cerebellar dysplasia, tethered cord and scoliosisLaura V Vandervore, Rachel Schot, A Jeannette M Hoogeboom, et al.
Leukemia Research|July 21, 2018
Erythropoietin levels and erythroid differentiation parameters in patients with lower-risk myelodysplastic syndromesC Gurnari, R Latagliata, F Buccisano, et al.
American Journal of Medical Genetics. Part A|February 16, 2005
Autosomal dominant inheritance of left ventricular outflow tract obstructionMarja W Wessels, Rolf M F Berger, Ingrid M E Frohn-Mulder, et al.
Human Mutation|November 14, 2008
Expanded mutational spectrum in Cohen syndrome, tissue expression, and transcript variants of COH1Wenke Seifert, Muriel Holder-Espinasse, Jirko Kühnisch, et al.
Nature|December 22, 2016
XRCC1 mutation is associated with PARP1 hyperactivation and cerebellar ataxiaNicolas C Hoch, Hana Hanzlikova, Stuart L Rulten, et al.
Clinical Genetics|February 18, 2014
Novel KDM6A (UTX) mutations and a clinical and molecular review of the X-linked Kabuki syndrome (KS2)S Banka, D Lederer, V Benoit, et al.
Journal of Cellular Biochemistry|October 3, 2022
Knockout of NRF2 triggers prostate cancer cells death through ROS modulation and sensitizes to cisplatinMariana C S Mancini, Ana P Morelli, Matheus B Severino, et al.
Environmental Research|November 19, 2023
Multi-target assessment of advanced oxidation processes-based strategies for indirect potable reuse of tertiary wastewater: Fate of compounds of emerging concerns, microbial and ecotoxicological parametersS Murgolo, O De Giglio, C De Ceglie, et al.
European Journal of Human Genetics : EJHG|November 11, 2010
The clinical spectrum of complete FBN1 allele deletionsYvonne Hilhorst-Hofstee, Ben C J Hamel, Joke B G M Verheij, et al.
Journal of Inherited Metabolic Disease|May 11, 2011
Long-term follow-up and treatment in nine boys with X-linked creatine transporter defectJiddeke M van de Kamp, Petra J W Pouwels, Femke K Aarsen, et al.
Pageof 35