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Clinical Genetics
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January 1, 1996
Homozygosity and heterozygosity for the transthyretin Leu64 mutation: clinical, biochemical and molecular findings
A Ferlini, F Salvi, A Uncini, et al.
Blood
|
November 24, 1999
Intrathymic restriction and peripheral expansion of the T-cell repertoire in Omenn syndrome
S Signorini, L Imberti, S Pirovano, et al.
Acta Bio-Medica De L'Ateneo Parmense : Organo Della Societa Di Medicina E Scienze Naturali Di Parma
|
January 1, 1984
[Analysis of the enzyme terminal deoxyribonucleotidyl transferase in lymphoma and leukemia cells]
E Bombardieri, F Campagnari, F De Braud, et al.
Breast Cancer Research and Treatment
|
March 13, 1998
Establishment and characterization of a new mammary adenocarcinoma cell line derived from MMTV neu transgenic mice
M G Sacco, L Gribaldo, O Barbieri, et al.
Molecular Cell
|
January 15, 2000
The RAG1/RAG2 complex constitutes a 3' flap endonuclease: implications for junctional diversity in V(D)J and transpositional recombination
S Santagata, E Besmer, A Villa, et al.
Calcified Tissue International
|
October 3, 2003
Association between a polymorphism affecting an AP1 binding site in the promoter of the TCIRG1 gene and bone mass in women
C Sobacchi, P Vezzoni, D M Reid, et al.
Gene Therapy
|
December 1, 1996
Partial regression, yet incomplete eradication of mammary tumors in transgenic mice by retrovirally mediated HSVtk transfer 'in vivo'
M G Sacco, S Benedetti, A Duflot-Dancer, et al.
Cell
|
June 18, 1998
Partial V(D)J recombination activity leads to Omenn syndrome
A Villa, S Santagata, F Bozzi, et al.
Genomics
|
October 14, 2000
Identification and characterization of an Xq26-q27 duplication in a family with spina bifida and panhypopituitarism suggests the involvement of two distinct genes
F A Hol, M T Schepens, S E van Beersum, et al.
British Journal of Haematology
|
September 30, 1998
Molecular and biochemical characterization of JAK3 deficiency in a patient with severe combined immunodeficiency over 20 years after bone marrow transplantation: implications for treatment
F Bozzi, G Lefranc, A Villa, et al.
Page
of 10
Search research articles
Search
Showing results (81-90 of 100) with videos related to
Sort By:
Page
of 10
Clinical Genetics
|
January 1, 1996
Homozygosity and heterozygosity for the transthyretin Leu64 mutation: clinical, biochemical and molecular findings
A Ferlini, F Salvi, A Uncini, et al.
Blood
|
November 24, 1999
Intrathymic restriction and peripheral expansion of the T-cell repertoire in Omenn syndrome
S Signorini, L Imberti, S Pirovano, et al.
Acta Bio-Medica De L'Ateneo Parmense : Organo Della Societa Di Medicina E Scienze Naturali Di Parma
|
January 1, 1984
[Analysis of the enzyme terminal deoxyribonucleotidyl transferase in lymphoma and leukemia cells]
E Bombardieri, F Campagnari, F De Braud, et al.
Breast Cancer Research and Treatment
|
March 13, 1998
Establishment and characterization of a new mammary adenocarcinoma cell line derived from MMTV neu transgenic mice
M G Sacco, L Gribaldo, O Barbieri, et al.
Molecular Cell
|
January 15, 2000
The RAG1/RAG2 complex constitutes a 3' flap endonuclease: implications for junctional diversity in V(D)J and transpositional recombination
S Santagata, E Besmer, A Villa, et al.
Calcified Tissue International
|
October 3, 2003
Association between a polymorphism affecting an AP1 binding site in the promoter of the TCIRG1 gene and bone mass in women
C Sobacchi, P Vezzoni, D M Reid, et al.
Gene Therapy
|
December 1, 1996
Partial regression, yet incomplete eradication of mammary tumors in transgenic mice by retrovirally mediated HSVtk transfer 'in vivo'
M G Sacco, S Benedetti, A Duflot-Dancer, et al.
Cell
|
June 18, 1998
Partial V(D)J recombination activity leads to Omenn syndrome
A Villa, S Santagata, F Bozzi, et al.
Genomics
|
October 14, 2000
Identification and characterization of an Xq26-q27 duplication in a family with spina bifida and panhypopituitarism suggests the involvement of two distinct genes
F A Hol, M T Schepens, S E van Beersum, et al.
British Journal of Haematology
|
September 30, 1998
Molecular and biochemical characterization of JAK3 deficiency in a patient with severe combined immunodeficiency over 20 years after bone marrow transplantation: implications for treatment
F Bozzi, G Lefranc, A Villa, et al.
Page
of 10