Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator CIITA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP292255.RAp27CvNi8VqysBrkysfAOwUgzbaZYh2sCxUesiXGswe4130_assertion description "[The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator CIITA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP292255.RAp27CvNi8VqysBrkysfAOwUgzbaZYh2sCxUesiXGswe4130_provenance.
• NP752943.RAsALq6Gv5aG-tBs3vTWkvyfxhlb5RzzFMdaPiFmSh5Bc130_assertion description "[The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator CIITA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP752943.RAsALq6Gv5aG-tBs3vTWkvyfxhlb5RzzFMdaPiFmSh5Bc130_provenance.
• NP232004.RAK09YIKsLp-V-IQ_GbHiTP9qnz26uc6EBOlvjW6Yiu3A130_assertion description "[The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator CIITA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP232004.RAK09YIKsLp-V-IQ_GbHiTP9qnz26uc6EBOlvjW6Yiu3A130_provenance.
• NP486806.RAZ2kmg7Wd66GQtrAc5KPB0rYRjUds8ADoYwWq5P-WMsw130_assertion description "[The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator CIITA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP486806.RAZ2kmg7Wd66GQtrAc5KPB0rYRjUds8ADoYwWq5P-WMsw130_provenance.
• NP618999.RAaYl_IWeO40TUrcByX5H1PSWhrshmEP3Nwed6P47YeD8130_assertion description "[The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator CIITA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP618999.RAaYl_IWeO40TUrcByX5H1PSWhrshmEP3Nwed6P47YeD8130_provenance.
• NP237538.RAJYdJaay41EIsCimu9xmE1ZIwdj7sBOu4yFE6O40mr_o130_assertion description "[The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator CIITA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237538.RAJYdJaay41EIsCimu9xmE1ZIwdj7sBOu4yFE6O40mr_o130_provenance.
• NP640953.RAy0hFZaJHXx9W2-Itj-H2ZYk_AxwD2xCpU4pXpcCetEs130_assertion description "[The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator CIITA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP640953.RAy0hFZaJHXx9W2-Itj-H2ZYk_AxwD2xCpU4pXpcCetEs130_provenance.
• NP742999.RA0_Zy71L7KEVHXEvXEKk7FosR9ofPIWYoivcdWCbA9HU130_assertion description "[The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator CIITA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP742999.RA0_Zy71L7KEVHXEvXEKk7FosR9ofPIWYoivcdWCbA9HU130_provenance.
• NP865339.RA16Ncpd5JRGSUvhBxuFlpLRHE5VJ1XqRb-L2Ppj9cYu0130_assertion description "[The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator CIITA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP865339.RA16Ncpd5JRGSUvhBxuFlpLRHE5VJ1XqRb-L2Ppj9cYu0130_provenance.
• NP860192.RA2GrvCEhv8DqwN23uwFebmf9QZOfZc5irYWoTkzPResQ130_assertion description "[The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator CIITA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP860192.RA2GrvCEhv8DqwN23uwFebmf9QZOfZc5irYWoTkzPResQ130_provenance.
• NP671624.RAUcRiGl8SgY1GpNVhNXfiY9XBckuhsEamot5uwkvJCMs130_assertion description "[The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator CIITA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP671624.RAUcRiGl8SgY1GpNVhNXfiY9XBckuhsEamot5uwkvJCMs130_provenance.
• NP671627.RAbwDHf5LP8oYPOoowAdAhLVnSuU3di-tJIZn4Aw7qNto130_assertion description "[The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator CIITA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP671627.RAbwDHf5LP8oYPOoowAdAhLVnSuU3di-tJIZn4Aw7qNto130_provenance.
• NP590045.RAFwErX2KfXW1WYBRJQUEw2krVOD6VeSzy0bqzjcLks0s130_assertion description "[The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator CIITA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP590045.RAFwErX2KfXW1WYBRJQUEw2krVOD6VeSzy0bqzjcLks0s130_provenance.
• assertion description "[The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator CIITA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP291728.RAWIoXnPX36u0Q8-Y4ihnAufcKXKkS5uRJZe0p9Djw_Po130_assertion description "[The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator CIITA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP291728.RAWIoXnPX36u0Q8-Y4ihnAufcKXKkS5uRJZe0p9Djw_Po130_provenance.
• NP671595.RAiReyFG0khO5OF9C67qmf7vKFNE-kmtR-QKepDdkfw3A130_assertion description "[The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator CIITA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP671595.RAiReyFG0khO5OF9C67qmf7vKFNE-kmtR-QKepDdkfw3A130_provenance.
• NP421541.RA0QSjdiTvNpThkbMVk21-zqjIm1ROM6IIzjwTPPlIde8130_assertion description "[The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator CIITA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP421541.RA0QSjdiTvNpThkbMVk21-zqjIm1ROM6IIzjwTPPlIde8130_provenance.
• NP556036.RAOxGLtVGUO2LPmkD7e8Sz2BC8DxGnLeDHb49Td_tUFH4130_assertion description "[The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator CIITA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP556036.RAOxGLtVGUO2LPmkD7e8Sz2BC8DxGnLeDHb49Td_tUFH4130_provenance.
• NP291726.RAEAQNax5JRXSXJvwA7rznp1NN2Voa__Fejq65gN3Ylfg130_assertion description "[The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator CIITA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP291726.RAEAQNax5JRXSXJvwA7rznp1NN2Voa__Fejq65gN3Ylfg130_provenance.
• NP291730.RALtsNRratGhNJx89d0V0K8SzafbKtEYPZgRzUjYLabbw130_assertion description "[The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator CIITA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP291730.RALtsNRratGhNJx89d0V0K8SzafbKtEYPZgRzUjYLabbw130_provenance.
• NP291732.RAPPcbVYmK22iD8_mUPwzxSXXmSjdAOjGdG_DAvVDJ2Q8130_assertion description "[The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator CIITA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP291732.RAPPcbVYmK22iD8_mUPwzxSXXmSjdAOjGdG_DAvVDJ2Q8130_provenance.
• NP671632.RAE71pMrkN6Kqznjr9T0-EllRAtkX7KgSd1kNpBa01vPc130_assertion description "[The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator CIITA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP671632.RAE71pMrkN6Kqznjr9T0-EllRAtkX7KgSd1kNpBa01vPc130_provenance.
• NP799383.RA7Yk4MOEZg4qnMgkW8W8kBN7gwUdnf-TA5R-2tKwZ7qU130_assertion description "[The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator CIITA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP799383.RA7Yk4MOEZg4qnMgkW8W8kBN7gwUdnf-TA5R-2tKwZ7qU130_provenance.
• NP291727.RA7zHKdKEQYRbi44nwlKDZEcNHZwrUQ3Bi77zOlmaOZ5Y130_assertion description "[The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator CIITA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP291727.RA7zHKdKEQYRbi44nwlKDZEcNHZwrUQ3Bi77zOlmaOZ5Y130_provenance.
• NP291729.RAy99e6OUlmIrz_iQFb-5tknnyvhqZTMuCYcJPi-2k2uc130_assertion description "[The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator CIITA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP291729.RAy99e6OUlmIrz_iQFb-5tknnyvhqZTMuCYcJPi-2k2uc130_provenance.
• NP291731.RAz9P9rdKFZH3WLjpBZ5osHWELRucPOZiNRcVZwWGxlh8130_assertion description "[The bare lymphocyte syndrome, a severe combined immunodeficiency due to loss of major histocompatibility complex (MHC) class II gene expression, is caused by inherited mutations in the genes encoding the heterotrimeric transcription factor RFX (RFX-B, RFX5, and RFXAP) and the class II transactivator CIITA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP291731.RAz9P9rdKFZH3WLjpBZ5osHWELRucPOZiNRcVZwWGxlh8130_provenance.