Zobrazeno 1 - 7
of 7
pro vyhledávání: '"G D, Montoya"'
Autor:
D, Feldman, J, Kearns, J, Wu, S, Bassinger, G D, Montoya, M, McKeen, S, Birkos, T M, Williams, M, Kamoun
Publikováno v:
Tissue antigens. 59(5)
Sequence specific oligonucleotide probe hybridization and sequence specific primer PCR typing of volunteer bone marrow donors suggested the presence of variants of known HLA-B alleles in two individuals. PCR products encompassing HLA-B locus exons 1,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::98240f1f139df78865798988c31fd019
https://pubmed.ncbi.nlm.nih.gov/12144629
https://pubmed.ncbi.nlm.nih.gov/12144629
Autor:
I S, Gourley, J, Kearns, J, Hou, J, Wu, S, Bassinger, G D, Montoya, M, McKeen, S, Birkos, T M, Williams, M, Kamoun
Publikováno v:
Tissue antigens. 58(3)
Sequence-specific oligonucleotide probe hybridization and sequence-specific primer polymerase chain reaction (PCR) typing of volunteer bone marrow donors suggested the presence of variants of known HLA-B alleles in five individuals. PCR products enco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0447c54b0b20683df09fb0d65a8ba056
https://pubmed.ncbi.nlm.nih.gov/11703832
https://pubmed.ncbi.nlm.nih.gov/11703832
Autor:
T M, Williams, J, Wu, S, Bassinger, G D, Montoya, J, Yee, B B, Griffith, J, Kearns, M, McKeen, S, Birkos, I S, Gourley, M, Kamoun
Publikováno v:
Tissue antigens. 55(5)
Several methods for low-resolution class I typing of potential bone marrow donors are available. The National Marrow Donor Program (NMDP) has initiated pilot projects for large-scale DNA-based class I typing to initially characterize donors. Sequence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9b59062679a5175cf223b7e4131a0164
https://pubmed.ncbi.nlm.nih.gov/10885568
https://pubmed.ncbi.nlm.nih.gov/10885568
Autor:
I S, Gourley, J, Wu, S, Bassinger, G D, Montoya, J, Yee, B B, Griffith, J, Kearns, M, McKeen, S, Birkos, T M, Williams, M, Kamoun
Publikováno v:
Tissue antigens. 55(4)
Sequence-specific oligonucleotide probe hybridization and sequence-specific primer polymerase chain reaction (PCR) typing suggested the presence of variants of HLA-B*40 in three individuals. Two were part of 3,500 potential marrow donors being screen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::01d18b2eb3bcf314d86e13721ffd3f83
https://pubmed.ncbi.nlm.nih.gov/10852391
https://pubmed.ncbi.nlm.nih.gov/10852391
Autor:
P J, Garry, R N, Baumgartner, S G, Brodie, G D, Montoya, H C, Liang, R D, Lindeman, T M, Williams
Publikováno v:
Clinical chemistry. 45(8 Pt 1)
Pharmacogenomics, the study of genetic loci that modulate drug responsiveness, may help to explain why estrogen replacement therapy (ERT) has differential effects on serum lipid and lipoprotein concentrations in postmenopausal women who inherit disti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a075f29fc6bb7332042ef23b69f9cbc3
https://pubmed.ncbi.nlm.nih.gov/10430787
https://pubmed.ncbi.nlm.nih.gov/10430787
Publikováno v:
The Journal of Immunology. 141:1161-1167
Preleptotene spermatocytes and spermatogonia are germ cells located outside the blood-testis barrier provided by the Sertoli cells. These cells have been found to express autoantigens accessible to circulating antibodies. Mice immunized with syngenei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4865561b8661f3d68dffaa926a50bce7
https://doi.org/10.4049/jimmunol.141.4.1161
https://doi.org/10.4049/jimmunol.141.4.1161
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950). 141(4)
Preleptotene spermatocytes and spermatogonia are germ cells located outside the blood-testis barrier provided by the Sertoli cells. These cells have been found to express autoantigens accessible to circulating antibodies. Mice immunized with syngenei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c0e8c10f869ea8189dc940565934e38b
https://pubmed.ncbi.nlm.nih.gov/3397538
https://pubmed.ncbi.nlm.nih.gov/3397538