Matches in Nanopublications for { ?s ?p "[In humans, however, loss-of-function mutations of TREM2/DAP12 leave myeloid cells unaffected but induce an autosomal recessive disease characterized, together with bone cysts, by a spectrum of pathological lesions in the cortex, thalamus and basal ganglia with clinical symptoms of progressive dementia (polycystic lipomembraneous osteodysplasia with sclerosing leukoencephalopathy).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP535660.RAVFPMMV9LIL1LLBKNUBtQIrdmhjpdATeZx-k9R6EbI6U130_assertion description "[In humans, however, loss-of-function mutations of TREM2/DAP12 leave myeloid cells unaffected but induce an autosomal recessive disease characterized, together with bone cysts, by a spectrum of pathological lesions in the cortex, thalamus and basal ganglia with clinical symptoms of progressive dementia (polycystic lipomembraneous osteodysplasia with sclerosing leukoencephalopathy).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP535660.RAVFPMMV9LIL1LLBKNUBtQIrdmhjpdATeZx-k9R6EbI6U130_provenance.
- NP922986.RARIMssONKe0VbAvdWvGzfZrWPcG8M9hv_bOraKDBmyVs130_assertion description "[In humans, however, loss-of-function mutations of TREM2/DAP12 leave myeloid cells unaffected but induce an autosomal recessive disease characterized, together with bone cysts, by a spectrum of pathological lesions in the cortex, thalamus and basal ganglia with clinical symptoms of progressive dementia (polycystic lipomembraneous osteodysplasia with sclerosing leukoencephalopathy).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP922986.RARIMssONKe0VbAvdWvGzfZrWPcG8M9hv_bOraKDBmyVs130_provenance.
- NP630234.RAowUULjmIyw5BAHHNZZHPD83UUps1VWKqKFCYjAjop1I130_assertion description "[In humans, however, loss-of-function mutations of TREM2/DAP12 leave myeloid cells unaffected but induce an autosomal recessive disease characterized, together with bone cysts, by a spectrum of pathological lesions in the cortex, thalamus and basal ganglia with clinical symptoms of progressive dementia (polycystic lipomembraneous osteodysplasia with sclerosing leukoencephalopathy).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP630234.RAowUULjmIyw5BAHHNZZHPD83UUps1VWKqKFCYjAjop1I130_provenance.
- NP898789.RA6NmM0Fa6XYVmVwVZqZSJtR28JMXr74t4pRyUBGLK_f4130_assertion description "[In humans, however, loss-of-function mutations of TREM2/DAP12 leave myeloid cells unaffected but induce an autosomal recessive disease characterized, together with bone cysts, by a spectrum of pathological lesions in the cortex, thalamus and basal ganglia with clinical symptoms of progressive dementia (polycystic lipomembraneous osteodysplasia with sclerosing leukoencephalopathy).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP898789.RA6NmM0Fa6XYVmVwVZqZSJtR28JMXr74t4pRyUBGLK_f4130_provenance.
- NP925923.RAz3trIxgcoikNzBwiLor_qaDci9FlaQ0ZVEzHHTHs0sU130_assertion description "[In humans, however, loss-of-function mutations of TREM2/DAP12 leave myeloid cells unaffected but induce an autosomal recessive disease characterized, together with bone cysts, by a spectrum of pathological lesions in the cortex, thalamus and basal ganglia with clinical symptoms of progressive dementia (polycystic lipomembraneous osteodysplasia with sclerosing leukoencephalopathy).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925923.RAz3trIxgcoikNzBwiLor_qaDci9FlaQ0ZVEzHHTHs0sU130_provenance.
- NP909526.RA0CuXgaL9x9IKV0vOTKA9Hz_eozYTF0_jvstMa-hr4u4130_assertion description "[In humans, however, loss-of-function mutations of TREM2/DAP12 leave myeloid cells unaffected but induce an autosomal recessive disease characterized, together with bone cysts, by a spectrum of pathological lesions in the cortex, thalamus and basal ganglia with clinical symptoms of progressive dementia (polycystic lipomembraneous osteodysplasia with sclerosing leukoencephalopathy).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP909526.RA0CuXgaL9x9IKV0vOTKA9Hz_eozYTF0_jvstMa-hr4u4130_provenance.
- NP764255.RAClkfdUm5TCfH031iUo_SJXwaxlfz9ON2-ntbVvJCsqE130_assertion description "[In humans, however, loss-of-function mutations of TREM2/DAP12 leave myeloid cells unaffected but induce an autosomal recessive disease characterized, together with bone cysts, by a spectrum of pathological lesions in the cortex, thalamus and basal ganglia with clinical symptoms of progressive dementia (polycystic lipomembraneous osteodysplasia with sclerosing leukoencephalopathy).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP764255.RAClkfdUm5TCfH031iUo_SJXwaxlfz9ON2-ntbVvJCsqE130_provenance.