Detalhe da pesquisa
1.
Fusion of intact human erythrocytes and erythrocyte ghosts.
J Cell Biol
; 63(1): 1-11, 1974 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-4371393
2.
Interconnected network of ganglion-like neural cell spheres formed on hydrozoan skeleton.
Tissue Eng
; 13(3): 473-82, 2007 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-17518598
3.
Triggered C-reactive protein (CRP) concentrations and the CRP gene -717A>G polymorphism in acute stroke or transient ischemic attack.
Eur J Neurol
; 14(3): 315-20, 2007 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-17355554
4.
Diversity of Glanzmann thrombasthenia in southern India: 10 novel mutations identified among 15 unrelated patients.
J Thromb Haemost
; 4(8): 1730-7, 2006 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-16879215
5.
Aragonite crystalline biomatrices support astrocytic tissue formation in vitro and in vivo.
Tissue Eng
; 12(7): 1763-73, 2006 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-16889507
6.
A 13-bp deletion in alpha(IIb) gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia.
J Thromb Haemost
; 3(12): 2764-72, 2005 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-16359514
7.
Time dependent protection of amifostine from renal and hematopoietic cisplatin induced toxicity.
Life Sci
; 76(16): 1825-34, 2005 Mar 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-15698860
8.
Mendelian diseases among Roman Jews: implications for the origins of disease alleles.
J Clin Endocrinol Metab
; 84(12): 4405-9, 1999 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-10599695
9.
Two p16 (CDKN2A) germline mutations in 30 Israeli melanoma families.
Eur J Hum Genet
; 8(8): 590-6, 2000 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-10951521
10.
A common ancestral mutation (C128X) occurring in 11 non-Jewish families from the UK with factor XI deficiency.
J Thromb Haemost
; 2(6): 918-24, 2004 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-15140127
11.
Detection of the Glanzmann's thrombasthenia mutations in Arab and Iraqi-Jewish patients by polymerase chain reaction and restriction analysis of blood or urine samples.
Thromb Haemost
; 66(4): 500-4, 1991 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-1796402
12.
Molecular characterization of four novel mutations causing factor VII deficiency.
Hematol J
; 1(6): 382-9, 2000.
Artigo
em Inglês
| MEDLINE | ID: mdl-11920218
13.
Cytokine network in nonresponding chronic hepatitis C patients with genotype 1: role of triple therapy with interferon alpha, ribavirin, and ursodeoxycholate.
Clin Biochem
; 34(3): 183-8, 2001 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-11408015
14.
The risk of fragile X premutation expansion is lower in carriers detected by general prenatal screening than in carriers from known fragile X families.
Genet Test
; 4(3): 289-92, 2000.
Artigo
em Inglês
| MEDLINE | ID: mdl-11142761
15.
[Macroenzymes: an interesting laboratory finding, without clinical relevance].
Harefuah
; 133(9): 359-62, 415, 1997 Nov 02.
Artigo
em Hebraico
| MEDLINE | ID: mdl-9418337
16.
Type I mutation in the F11 gene is a third ancestral mutation which causes factor XI deficiency in Ashkenazi Jews.
J Thromb Haemost
; 11(4): 724-30, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23332144
17.
Search for genetic variants associated with cutaneous malignant melanoma in the Ashkenazi Jewish population.
J Med Genet
; 42(5): e30, 2005 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-15863662
18.
Point mutations regarded as missense mutations cause splicing defects in the factor XI gene.
J Thromb Haemost
; 9(10): 1977-84, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21718436
19.
Glanzmann thrombasthenia: new insights from an historical perspective.
Semin Hematol
; 31(4): 301-11, 1994 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-7831575
20.
Molecular biology techniques in the diagnosis of monogenic diseases.
Clin Chim Acta
; 225(1): S35-50, 1994 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-8033350