21
TITLE: Stable recombinant expression and characterization of the two haemophilic factor VIII variants C329S (CRM-) and G1948D (CRMr)  Full Text
AUTHORS: David, D; Saenko, EL; Santos, IMA; Johnson, DJD; Tuddenham, EGD; McVey, JH; Kemball Cook, G;
PUBLISHED: 2001, SOURCE: BRITISH JOURNAL OF HAEMATOLOGY, VOLUME: 113, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
22
TITLE: Mutations in alpha PIX, encoding a guanine nucleotide exchange factor for Rho GT-Pases, in patients with X-linked mental retardation.
AUTHORS: Kutsche, K; Yntema, H; Brandt, A; Jantke, I; Nothwang, HG; Orth, U; Boavida, MG; David, D; Moraine, C; Ropers, HH; van Bokhoven, H; Gal, A;
PUBLISHED: 2000, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 67, ISSUE: 4
INDEXED IN: WOS
23
TITLE: Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardation  Full Text
AUTHORS: Kutsche, K; Yntema, H; Brandt, A; Jantke, I; Nothwang, HG; Orth, U; Boavida, MG; David, D; Chelly, J; Fryns, JP; Moraine, C; Ropers, HH; Hamel, BCJ; van Bokhoven, H; Gal, A;
PUBLISHED: 2000, SOURCE: NATURE GENETICS, VOLUME: 26, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef
IN MY: ORCID
24
TITLE: Characterization of a splicing mutation in the factor VIII gene at the RNA level
AUTHORS: Dezs� David; Alice Tavares; Joao Lavinha;
PUBLISHED: 1995, SOURCE: Human Genetics, VOLUME: 95, ISSUE: 1
INDEXED IN: CrossRef: 9
IN MY: ORCID
25
TITLE: ANALYSIS OF THE ESSENTIAL SEQUENCES OF THE FACTOR-VIII GENE IN 12 HEMOPHILIA-A PATIENTS BY SINGLE-STRANDED CONFORMATION POLYMORPHISM
AUTHORS: DAVID, D; MOREIRA, I; LALLOZ, MRA; ROSA, HAV; SCHWAAB, R; MORAIS, S; DINIZ, MJ; DEDEUS, G; CAMPOS, M; LAVINHA, J; JOHNSON, D; TUDDENHAM, EGD;
PUBLISHED: 1994, SOURCE: BLOOD COAGULATION & FIBRINOLYSIS, VOLUME: 5, ISSUE: 2
INDEXED IN: Scopus WOS
26
TITLE: Single-strand conformation polymorphism (SSCP) analysis of the molecular pathology of hemophilia B
AUTHORS: Dezso David; Humberto A V Rosa; Susan Pemberton; Maria J Diniz; Manuel Campos; João Lavinha;
PUBLISHED: 1993, SOURCE: Human Mutation - Hum. Mutat., VOLUME: 2, ISSUE: 5
INDEXED IN: CrossRef
IN MY: ORCID
27
TITLE: Molecular Analysis and Genetic Mapping of the Rhodopsin Gene in Families with Autosomal Dominant Retinitis Pigmentosa  Full Text
AUTHORS: Bunge, S; Wedemann, H; David, D; D.J Terwilliger; L.I van den Born; Aulehla-Scholz, C; Samanns, C; Horn, M; Ott, J; Schwinger, E; Schinzel, A; M.J Denton; Gal, A;
PUBLISHED: 1993, SOURCE: Genomics, VOLUME: 17, ISSUE: 1
INDEXED IN: CrossRef
IN MY: ORCID
28
TITLE: Parental origin of extra chromosomes in persons with X chromosome tetrasomy.
AUTHORS: David, D; Marques, RA; Carreiro, MH; Moreira, I; Boavida, MG;
PUBLISHED: 1992, SOURCE: Journal of Medical Genetics, VOLUME: 29, ISSUE: 8
INDEXED IN: CrossRef
IN MY: ORCID
29
TITLE: Regulation of Liver Gene Expression in Dexamethasone Resistant Hepatoma Cells
AUTHORS: Venetianer, A; David, D;
PUBLISHED: 1990, SOURCE: Activation of Hormone and Growth Factor Receptors
INDEXED IN: CrossRef: 1
IN MY: ORCID
Page 3 of 3. Total results: 29.