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1 fan anemia (DBA) is a cancer-prone inherited bone marrow failure syndrome.
2 of Shwachman-Diamond syndrome, an inherited bone marrow failure syndrome.
3 keratosis congenita (DC) is a rare inherited bone marrow failure syndrome.
4 ality among hematopoietic stem cells in this bone marrow failure syndrome.
5 d to define the relationship between PNH and bone marrow failure syndromes.
6 e development of hematologic malignancies or bone marrow failure syndromes.
7 s in the 5q-syndrome, DBA, and perhaps other bone marrow failure syndromes.
8 rited and acquired red cell disorders and in bone marrow failure syndromes.
9 ologic disease, is the paradigm of the human bone marrow failure syndromes.
10 A DRB1 locus is a marker for immune-mediated bone marrow failure syndromes.
11 aplastic anemia and other cytokine-mediated bone marrow failure syndromes.
12 e treatment of aplastic anemia and inherited bone marrow failure syndromes.
13 n implicated in the pathophysiology of human bone marrow failure syndromes.
14 lar causes have been recognized to result in bone marrow failure syndromes: (1) defects in the Fancon
16 eratosis congenita, DBA is both an inherited bone marrow failure syndrome and a cancer predisposition
17 ubiquitination of FANCD2 was normal in other bone marrow failure syndromes and chromosomal breakage s
18 ome of CD34 cells derived from patients with bone marrow failure syndromes and identified characteris
19 sm of clonal selection and leukemogenesis in bone marrow failure syndromes and our data suggest that
20 me synthesis may contribute to each of these bone marrow failure syndromes (and perhaps others), prec
22 have recently shown that some patients with bone marrow failure syndromes are heterozygous carriers
26 Dyskeratosis congenita (DC) is an inherited bone marrow failure syndrome associated with increased c
27 wachman-Diamond syndrome (SDS), an inherited bone marrow failure syndrome associated with leukemia pr
28 ribosomal subunit maturation to an inherited bone marrow failure syndrome associated with leukemia pr
31 this reverse transcriptase is mutated in the bone marrow failure syndrome autosomal dominant dyskerat
32 to dyskeratosis congenita (DC), an inherited bone marrow failure syndrome caused by defects in telome
33 linked dyskeratosis congenita (DC) is a rare bone marrow failure syndrome caused by mostly missense m
34 X-linked dyskeratosis congenita (DC) is a bone marrow failure syndrome caused by mutations in the
35 amond Blackfan anaemia (DBA) is a congenital bone marrow failure syndrome characterised by selective
37 Dyskeratosis congenita (DC) is a multisystem bone marrow failure syndrome characterized by a triad of
38 Dyskeratosis congenita (DC) is a multisystem bone marrow failure syndrome characterized by a triad of
39 Diamond-Blackfan anemia (DBA), an inherited bone marrow failure syndrome characterized by anemia tha
41 Dyskeratosis congenita (DC) is an inherited bone marrow failure syndrome characterized by cutaneous
42 iamond Blackfan anemia (DBA) is an inherited bone marrow failure syndrome characterized by erythroid
43 iamond-Blackfan anemia (DBA) is a congenital bone marrow failure syndrome characterized by erythroid
44 TERT and hTR cause dyskeratosis congenita, a bone marrow failure syndrome characterized by mucocutane
45 iamond Blackfan anemia (DBA) is an inherited bone marrow failure syndrome characterized by red cell a
47 gy to create a mouse model for the inherited bone marrow failure syndrome, DBA.The result, while reca
48 vely, these observations identify a distinct bone-marrow-failure syndrome due to mutations in ERCC6L2
51 an gene encoding dyskerin cause the skin and bone marrow failure syndrome dyskeratosis congenita (DC)
52 erase deficiency in the X-linked form of the bone marrow failure syndrome dyskeratosis congenita, mut
54 nifestations of telomere disease include the bone marrow failure syndromes dyskeratosis congenita and
55 riptase, telomerase, are associated with the bone marrow failure syndromes dyskeratosis congenita, ap
56 , the protein defective in patients with the bone marrow failure syndrome Fanconi anemia complementat
59 is congenita (DC), a heterogeneous inherited bone marrow failure syndrome, have abnormalities in telo
60 ome (SDS) (OMIM #260400) is a rare inherited bone marrow failure syndrome (IBMFS) that is primarily c
62 Dyskeratosis congenita (DC) is an inherited bone marrow failure syndrome in which the known suscepti
63 ng their contributions to the development of bone marrow failure syndromes in Tak1-knockout mice (Tak
64 tibody-based immunosuppressive treatment for bone marrow failure syndromes in the absence of transpla
65 -Hreidarsson syndrome (HHS), are multisystem bone-marrow-failure syndromes in which the principal pat
66 for certain aspects of the pathology seen in bone marrow failure syndromes, including aplastic anemia
67 addition of SDS to the growing list of human bone marrow failure syndromes involving the ribosome.
70 nd syndrome (SDS; OMIM 260400), an inherited bone marrow failure syndrome, is caused by mutations in
71 eratosis congenita (AD DC), a rare inherited bone marrow failure syndrome, is caused by mutations in
72 stic anemia, the paradigm of immune-mediated bone marrow failure syndromes, is characterized by hemat
73 Diamond-Blackfan anemia (DBA), a congenital bone-marrow-failure syndrome, is characterized by red bl
75 needed to identify genes causally related to bone marrow failure syndromes, myelodysplastic syndromes
77 emia at older age is complex and ranges from bone marrow failure syndromes to chronic kidney disease,
78 congenital neutropenia (CN) is a preleukemic bone marrow failure syndrome with a 20% risk of evolving
79 Androgens have been used in the treatment of bone marrow failure syndromes without a clear understand
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