ライフサイエンスコーパス: platelet disorder

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1 a previously undescribed dominant Mendelian platelet disorder.

2 edicine and in high turnover/high activation platelet disorders.

3 a spectrum of congenital red blood cell and platelet disorders.

4 the management of thrombocytopenia and other platelet disorders.

5 oter-driven MuLV vectors for gene therapy of platelet disorders.

6 l applications toward human gene therapy for platelet disorders.

7 in platelet production can lead to inherited platelet disorders.

8 ts of patients with constitutional (familial platelet disorder/acute myeloid leukemia) or acquired (c

9 matologic malignancies that include familial platelet disorder/acute myeloid leukemia, primary or sec

10 similar to that seen in patients with Quebec platelet disorder, affirming the role of ectopic urokina

11 a large pedigree with an autosomal dominant platelet disorder and a striking propensity in affected

12 a new and simple tool to identify inherited platelet disorders and myeloid neoplasms with abnormalit

13 ng the mutant loci in a variety of inherited platelet disorders, and these findings are beginning to

14 Some familial platelet disorders are associated with predisposition to

15 elet membrane is the cause of the congenital platelet disorder Bernard-Soulier syndrome (BSS).

16 nrelated families in the BRIDGE Bleeding and Platelet Disorders (BPD) collection who carry a TPM4 var

17 Glanzmann thrombasthenia (GT), an inherited platelet disorder caused by mutations in integrin alphaI

18 s with ITP seen at the New York Presbyterian Platelet Disorder Center in the past 10 years.

19 Glanzmann's thrombasthenia is a qualitative platelet disorder characterized by a deficiency in the p

20 FPD/AML is a familial platelet disorder characterized by platelet defects, pre

21 To prevent and treat immune-mediated platelet disorders (e.g. neonatal allo-immune thrombocyt

22 nic sequestration and destruction in various platelet disorders, especially idiopathic thrombocytopen

23 For patients with inherited platelet disorders, ex vivo-generated platelets offer th

24 One rare example of a platelet disorder, Glanzmann thrombasthenia (GT), is cha

25 In certain forms of the inherited platelet disorder, Glanzmann thrombasthenia (GT), mutant

26 Platelet disorders have been successfully modeled and ge

27 1-3p22.1 has not been previously linked to a platelet disorder; identification of the GPS gene will l

28 ing actin dynamics have been associated with platelet disorders in humans and mice.

29 harboring variants responsible for inherited platelet disorders (IPDs).

30 By implication, in patients experiencing platelet disorders, platelet (dys)function is almost com

31 appears to be an additional and (at least in platelet disorders) -possibly clinically relevant mechan

32 malities in human patients with the familial platelet disorder resulting from AML1 haploinsufficiency

33 syndrome (GPS) is a predominantly recessive platelet disorder that is characterized by mild thromboc

34 stian (SBS) syndromes are autosomal dominant platelet disorders that share macrothrombocytopenia and

35 on factor RUNX1 are associated with familial platelet disorder, thrombocytopenia, and predisposition

36 report the linkage of the autosomal dominant platelet disorder to markers on chromosome 21q22.

37 es in pedigrees with unexplained bleeding or platelet disorders to data from 5422 controls.

38 It belongs to a group of hereditary platelet disorders typified by normal platelet numbers a

39 The nature of an inherited platelet disorder was investigated in three siblings aff

40 e protease neutrophil elastase, and familial platelet disorder with acute myelogenous leukemia (AML),

41 ion domain, found in a patient with familial platelet disorder with AML, fails to stimulate the ELA2

42 Monoallelic RUNX1 mutations cause familial platelet disorder with predisposition for acute myelogen

43 Familial platelet disorder with predisposition to acute myelogeno

44 Familial platelet disorder with predisposition to acute myeloid l

45 a (AML) and in association with the familial platelet disorder with propensity to develop AML (FPD/AM

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