Search research articles
Contact Us
Filters
Showing results (21-30 of 135) with videos related to
Page
of 14
Sort By:
Molecular Cancer Research : MCR
|
September 13, 2006
Nuclear factor Y drives basal transcription of the human TLX3, a gene overexpressed in T-cell acute lymphocytic leukemia
Silvia Borghini, Manuela Vargiolu, Marco Di Duca, et al.
Experimental Cell Research
|
April 18, 2015
Identification of novel pathways and molecules able to down-regulate PHOX2B gene expression by in vitro drug screening approaches in neuroblastoma cells
Eleonora Di Zanni, Diego Fornasari, Roberto Ravazzolo, et al.
European Journal of Human Genetics : EJHG
|
October 3, 2008
Mutational analysis of the ACVR1 gene in Italian patients affected with fibrodysplasia ossificans progressiva: confirmations and advancements
Renata Bocciardi, Domenico Bordo, Marco Di Duca, et al.
The Biochemical Journal
|
April 11, 2013
TMEM16A-TMEM16B chimaeras to investigate the structure-function relationship of calcium-activated chloride channels
Paolo Scudieri, Elvira Sondo, Emanuela Caci, et al.
Medycyna Wieku Rozwojowego
|
August 9, 2005
[Clinical picture and molecular analysis in a familial case of Nail-Patella Syndrome--identification of a new mutation in LMX1B gene]
Krzysztof Szczałuba, Ewa Obersztyn, Kazimierz Kozłowski, et al.
Gene Expression
|
July 3, 2003
The first intron of the human osteopontin gene contains a C/EBP-beta-responsive enhancer
Francesca Giacopelli, Nadia Rosatto, Maria Teresa Divizia, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
February 22, 2011
Low amounts of PHOX2B expanded alleles in asymptomatic parents suggest unsuspected recurrence risk in congenital central hypoventilation syndrome
Tiziana Bachetti, Sara Parodi, Marco Di Duca, et al.
BMB Reports
|
January 5, 2010
Functional characterization of a minimal sequence essential for the expression of human TLX2 gene
Silvia Borghini, Tiziana Bachetti, Monica Fava, et al.
Oncotarget
|
October 27, 2017
Targeting of <i>PHOX2B</i> expression allows the identification of drugs effective in counteracting neuroblastoma cell growth
Eleonora Di Zanni, Giovanna Bianchi, Roberto Ravazzolo, et al.
Human Molecular Genetics
|
May 13, 2005
Distinct pathogenetic mechanisms for PHOX2B associated polyalanine expansions and frameshift mutations in congenital central hypoventilation syndrome
Tiziana Bachetti, Ivana Matera, Silvia Borghini, et al.
Page
of 14
Search research articles
Search
Showing results (21-30 of 135) with videos related to
Sort By:
Page
of 14
Molecular Cancer Research : MCR
|
September 13, 2006
Nuclear factor Y drives basal transcription of the human TLX3, a gene overexpressed in T-cell acute lymphocytic leukemia
Silvia Borghini, Manuela Vargiolu, Marco Di Duca, et al.
Experimental Cell Research
|
April 18, 2015
Identification of novel pathways and molecules able to down-regulate PHOX2B gene expression by in vitro drug screening approaches in neuroblastoma cells
Eleonora Di Zanni, Diego Fornasari, Roberto Ravazzolo, et al.
European Journal of Human Genetics : EJHG
|
October 3, 2008
Mutational analysis of the ACVR1 gene in Italian patients affected with fibrodysplasia ossificans progressiva: confirmations and advancements
Renata Bocciardi, Domenico Bordo, Marco Di Duca, et al.
The Biochemical Journal
|
April 11, 2013
TMEM16A-TMEM16B chimaeras to investigate the structure-function relationship of calcium-activated chloride channels
Paolo Scudieri, Elvira Sondo, Emanuela Caci, et al.
Medycyna Wieku Rozwojowego
|
August 9, 2005
[Clinical picture and molecular analysis in a familial case of Nail-Patella Syndrome--identification of a new mutation in LMX1B gene]
Krzysztof Szczałuba, Ewa Obersztyn, Kazimierz Kozłowski, et al.
Gene Expression
|
July 3, 2003
The first intron of the human osteopontin gene contains a C/EBP-beta-responsive enhancer
Francesca Giacopelli, Nadia Rosatto, Maria Teresa Divizia, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
February 22, 2011
Low amounts of PHOX2B expanded alleles in asymptomatic parents suggest unsuspected recurrence risk in congenital central hypoventilation syndrome
Tiziana Bachetti, Sara Parodi, Marco Di Duca, et al.
BMB Reports
|
January 5, 2010
Functional characterization of a minimal sequence essential for the expression of human TLX2 gene
Silvia Borghini, Tiziana Bachetti, Monica Fava, et al.
Oncotarget
|
October 27, 2017
Targeting of <i>PHOX2B</i> expression allows the identification of drugs effective in counteracting neuroblastoma cell growth
Eleonora Di Zanni, Giovanna Bianchi, Roberto Ravazzolo, et al.
Human Molecular Genetics
|
May 13, 2005
Distinct pathogenetic mechanisms for PHOX2B associated polyalanine expansions and frameshift mutations in congenital central hypoventilation syndrome
Tiziana Bachetti, Ivana Matera, Silvia Borghini, et al.
Page
of 14