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Acta Geneticae Medicae Et Gemellologiae
|
January 1, 1977
Plasma protein variability in monozygotic twins: further studies and applications
M Milani-Comparetti, F Britti, D Casini, et al.
Blood
|
August 15, 2000
Human erythrocyte pyrimidine 5-nucleotidase, PN-I, is identical to p36, a protein associated to lupus inclusion formation in response to alpha-interferon
A Amici, M Emanuelli, N Raffaelli, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale
|
February 1, 1993
Establishment and characterization of two human small cell lung carcinoma cell lines
E Recanatini, F Marcheggiani, G Corinaldesi, et al.
The Journal of Biological Chemistry
|
January 5, 1996
Molecular cloning, heterologous expression, and characterization of human glyoxalase II
M Ridderström, F Saccucci, U Hellman, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale
|
March 30, 1980
[Incidence of the qh+ varients in the karyotype of subjects occupationally exposed to ionizing radiations]
M Milani-Comparetti, Q Catena, D Donati, et al.
Pregnancy Hypertension
|
June 25, 2015
PP035. Placental klotho protein in preeclampsia: A possible link to long term outcomes
S R Giannubilo, M Cecati, F Saccucci, et al.
Biochemistry and Molecular Biology International
|
May 19, 1998
Structural characterization of human glyoxalase II as probed by limited proteolysis
A Aceto, B Dragani, S Melino, et al.
The Journal of Biological Chemistry
|
October 12, 2000
Molecular cloning, chromosomal localization, tissue mRNA levels, bacterial expression, and enzymatic properties of human NMN adenylyltransferase
M Emanuelli, F Carnevali, F Saccucci, et al.
Acta Geneticae Medicae Et Gemellologiae
|
January 1, 1975
A case of "g 2 deletion syndrome": ring or partial monosomy? (46,XX,22r or 46,XX,22p- ?)
M Milani-Comparetti, V Rossolini, D P Pace, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale
|
August 30, 1983
Frequency of qh+ chromosomal variants in a) radioexposed, b) Down syndrome and c) control subjects
F Saccucci, Q Catena, F Dolcini, et al.
Page
of 3
Search research articles
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Showing results (11-20 of 27) with videos related to
Sort By:
Page
of 3
Acta Geneticae Medicae Et Gemellologiae
|
January 1, 1977
Plasma protein variability in monozygotic twins: further studies and applications
M Milani-Comparetti, F Britti, D Casini, et al.
Blood
|
August 15, 2000
Human erythrocyte pyrimidine 5-nucleotidase, PN-I, is identical to p36, a protein associated to lupus inclusion formation in response to alpha-interferon
A Amici, M Emanuelli, N Raffaelli, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale
|
February 1, 1993
Establishment and characterization of two human small cell lung carcinoma cell lines
E Recanatini, F Marcheggiani, G Corinaldesi, et al.
The Journal of Biological Chemistry
|
January 5, 1996
Molecular cloning, heterologous expression, and characterization of human glyoxalase II
M Ridderström, F Saccucci, U Hellman, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale
|
March 30, 1980
[Incidence of the qh+ varients in the karyotype of subjects occupationally exposed to ionizing radiations]
M Milani-Comparetti, Q Catena, D Donati, et al.
Pregnancy Hypertension
|
June 25, 2015
PP035. Placental klotho protein in preeclampsia: A possible link to long term outcomes
S R Giannubilo, M Cecati, F Saccucci, et al.
Biochemistry and Molecular Biology International
|
May 19, 1998
Structural characterization of human glyoxalase II as probed by limited proteolysis
A Aceto, B Dragani, S Melino, et al.
The Journal of Biological Chemistry
|
October 12, 2000
Molecular cloning, chromosomal localization, tissue mRNA levels, bacterial expression, and enzymatic properties of human NMN adenylyltransferase
M Emanuelli, F Carnevali, F Saccucci, et al.
Acta Geneticae Medicae Et Gemellologiae
|
January 1, 1975
A case of "g 2 deletion syndrome": ring or partial monosomy? (46,XX,22r or 46,XX,22p- ?)
M Milani-Comparetti, V Rossolini, D P Pace, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale
|
August 30, 1983
Frequency of qh+ chromosomal variants in a) radioexposed, b) Down syndrome and c) control subjects
F Saccucci, Q Catena, F Dolcini, et al.
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of 3