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Cintia Fridman

Showing results (11-20 of 24) with videos related to

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Epilepsia|July 31, 2003
Angelman syndrome: difficulties in EEG pattern recognition and possible misinterpretationsKette D Valente, Joaquina Q Andrade, Rosi M Grossmann, et al.
Forensic Science International. Genetics|December 17, 2008
Brazilian population profile of 15 STR markersCintia Fridman, Paulo César Costa dos Santos, Priscila Kohler, et al.
Epilepsy Research|October 18, 2005
Angelman syndrome: uniparental paternal disomy 15 determines mild epilepsy, but has no influence on EEG patternsKette D Valente, Cintia Fridman, Monica C Varela, et al.
Journal of Community Genetics|November 27, 2024
Motivations, perceptions and impacts of direct-to-consumer genetic testing among users in BrazilLarissa Siqueira Penna, Raphael Bruno Amemiya, Thiago Pires, et al.
In Vitro Cellular & Developmental Biology. Animal|December 10, 2009
Establishment and characterization of androgen-independent human prostate cancer cell lines, PcBra1, PcBra2, and PcBra3Camila B Piantino, Juliana M Sousa-Canavez, Marta Bellodi-Privato, et al.
European Archives of Psychiatry and Clinical Neuroscience|March 29, 2003
Association of a new polymorphism in ALOX12 gene with bipolar disorderCintia Fridman, Elida P B Ojopi, Sheila P Gregório, et al.
International Journal of Legal Medicine|February 28, 2025
Uniparental disomy (UPD) as the cause of inconsistencies in parentage tests: report of maternal UPD of chromosome 2 and review of the literatureCintia Fridman, João Paulo Gervasio Batista, Pamela Viana Bianchini, et al.
Genetics and Molecular Biology|June 8, 2017
Growth hormone insensitivity with immune dysfunction caused by a STAT5B mutation in the south of Brazil: evidence for a founder effectRenata C Scalco, Fernanda T Gonçalves, Hadassa C Santos, et al.
In Vitro Cellular & Developmental Biology. Animal|November 17, 2009
Establishment and characterization of human bladder cancer cell lines BexBra1, BexBra2, and BexBra4Camila B Piantino, Juliana M Sousa-Canavez, Victor Srougi, et al.
American Journal of Medical Genetics. Part A|March 26, 2014
The E180splice mutation in the GHR gene causing Laron syndrome: witness of a Sephardic Jewish exodus from the Iberian Peninsula to the New World?Fernanda T Gonçalves, Cintia Fridman, Emília M Pinto, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Epilepsia|July 31, 2003
Angelman syndrome: difficulties in EEG pattern recognition and possible misinterpretationsKette D Valente, Joaquina Q Andrade, Rosi M Grossmann, et al.
Forensic Science International. Genetics|December 17, 2008
Brazilian population profile of 15 STR markersCintia Fridman, Paulo César Costa dos Santos, Priscila Kohler, et al.
Epilepsy Research|October 18, 2005
Angelman syndrome: uniparental paternal disomy 15 determines mild epilepsy, but has no influence on EEG patternsKette D Valente, Cintia Fridman, Monica C Varela, et al.
Journal of Community Genetics|November 27, 2024
Motivations, perceptions and impacts of direct-to-consumer genetic testing among users in BrazilLarissa Siqueira Penna, Raphael Bruno Amemiya, Thiago Pires, et al.
In Vitro Cellular & Developmental Biology. Animal|December 10, 2009
Establishment and characterization of androgen-independent human prostate cancer cell lines, PcBra1, PcBra2, and PcBra3Camila B Piantino, Juliana M Sousa-Canavez, Marta Bellodi-Privato, et al.
European Archives of Psychiatry and Clinical Neuroscience|March 29, 2003
Association of a new polymorphism in ALOX12 gene with bipolar disorderCintia Fridman, Elida P B Ojopi, Sheila P Gregório, et al.
International Journal of Legal Medicine|February 28, 2025
Uniparental disomy (UPD) as the cause of inconsistencies in parentage tests: report of maternal UPD of chromosome 2 and review of the literatureCintia Fridman, João Paulo Gervasio Batista, Pamela Viana Bianchini, et al.
Genetics and Molecular Biology|June 8, 2017
Growth hormone insensitivity with immune dysfunction caused by a STAT5B mutation in the south of Brazil: evidence for a founder effectRenata C Scalco, Fernanda T Gonçalves, Hadassa C Santos, et al.
In Vitro Cellular & Developmental Biology. Animal|November 17, 2009
Establishment and characterization of human bladder cancer cell lines BexBra1, BexBra2, and BexBra4Camila B Piantino, Juliana M Sousa-Canavez, Victor Srougi, et al.
American Journal of Medical Genetics. Part A|March 26, 2014
The E180splice mutation in the GHR gene causing Laron syndrome: witness of a Sephardic Jewish exodus from the Iberian Peninsula to the New World?Fernanda T Gonçalves, Cintia Fridman, Emília M Pinto, et al.
Pageof 3