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Clinical Genetics
|
September 5, 2015
Mutation spectrum of the MTM1 gene in XLMTM patients: 10 years of experience in prenatal and postnatal diagnosis
G Longo, S Russo, G Novelli, et al.
Neuron
|
July 1, 1994
Orthopedia, a novel homeobox-containing gene expressed in the developing CNS of both mouse and Drosophila
A Simeone, M R D'Apice, V Nigro, et al.
The EMBO Journal
|
July 1, 1993
A vertebrate gene related to orthodenticle contains a homeodomain of the bicoid class and demarcates anterior neuroectoderm in the gastrulating mouse embryo
A Simeone, D Acampora, A Mallamaci, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
January 9, 2008
Diagnosis of atypical CF: a case-report to reflect
F Alghisi, A Angioni, A C Tomaiuolo, et al.
European Review for Medical and Pharmacological Sciences
|
August 4, 2017
Prevention of neural tube defects and maternal gestational diabetes through the inositol supplementation: preliminary results
D Dell'Edera, F Sarlo, A Allegretti, et al.
Clinical and Experimental Medicine
|
December 28, 2006
Gene expression profile study in CFTR mutated bronchial cell lines
S Gambardella, M Biancolella, M R D'Apice, et al.
Clinical Genetics
|
June 17, 2008
Increased release and activity of matrix metalloproteinase-9 in patients with mandibuloacral dysplasia type A, a rare premature ageing syndrome
F Lombardi, G F Fasciglione, M R D'Apice, et al.
Gene
|
January 17, 2015
Clinical and molecular spectra in galactosemic patients from neonatal screening in northeastern Italy: structural and functional characterization of new variations in the galactose-1-phosphate uridyltransferase (GALT) gene
E Viggiano, A Marabotti, A P Burlina, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
February 19, 2008
Epidemiology and a novel procedure for large scale analysis of CFTR rearrangements in classic and atypical CF patients: a multicentric Italian study
R Tomaiuolo, F Sangiuolo, C Bombieri, et al.
European Journal of Histochemistry : EJH
|
February 3, 2012
Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria
V Cenni, C Capanni, M Columbaro, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 13) with videos related to
Sort By:
Page
of 2
Clinical Genetics
|
September 5, 2015
Mutation spectrum of the MTM1 gene in XLMTM patients: 10 years of experience in prenatal and postnatal diagnosis
G Longo, S Russo, G Novelli, et al.
Neuron
|
July 1, 1994
Orthopedia, a novel homeobox-containing gene expressed in the developing CNS of both mouse and Drosophila
A Simeone, M R D'Apice, V Nigro, et al.
The EMBO Journal
|
July 1, 1993
A vertebrate gene related to orthodenticle contains a homeodomain of the bicoid class and demarcates anterior neuroectoderm in the gastrulating mouse embryo
A Simeone, D Acampora, A Mallamaci, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
January 9, 2008
Diagnosis of atypical CF: a case-report to reflect
F Alghisi, A Angioni, A C Tomaiuolo, et al.
European Review for Medical and Pharmacological Sciences
|
August 4, 2017
Prevention of neural tube defects and maternal gestational diabetes through the inositol supplementation: preliminary results
D Dell'Edera, F Sarlo, A Allegretti, et al.
Clinical and Experimental Medicine
|
December 28, 2006
Gene expression profile study in CFTR mutated bronchial cell lines
S Gambardella, M Biancolella, M R D'Apice, et al.
Clinical Genetics
|
June 17, 2008
Increased release and activity of matrix metalloproteinase-9 in patients with mandibuloacral dysplasia type A, a rare premature ageing syndrome
F Lombardi, G F Fasciglione, M R D'Apice, et al.
Gene
|
January 17, 2015
Clinical and molecular spectra in galactosemic patients from neonatal screening in northeastern Italy: structural and functional characterization of new variations in the galactose-1-phosphate uridyltransferase (GALT) gene
E Viggiano, A Marabotti, A P Burlina, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
February 19, 2008
Epidemiology and a novel procedure for large scale analysis of CFTR rearrangements in classic and atypical CF patients: a multicentric Italian study
R Tomaiuolo, F Sangiuolo, C Bombieri, et al.
European Journal of Histochemistry : EJH
|
February 3, 2012
Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria
V Cenni, C Capanni, M Columbaro, et al.
Page
of 2