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Results: 1-14 |
Results: 14
Ethiopian exodus: A practice journal.
Authors: Nichols, WC
Citation: Wc. Nichols, Ethiopian exodus: A practice journal., CONT FAM TH, 23(1), 2001, pp. 147-149
Creative conversations: Meetings with family therapists and their ideas [Skapande konversationr].
Authors: Nichols, WC
Citation: Wc. Nichols, Creative conversations: Meetings with family therapists and their ideas [Skapande konversationr]., CONT FAM TH, 23(1), 2001, pp. 149-150
Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasia
Authors: Trembath, RC Thomson, JR Machado, RD Morgan, NV Atkinson, C Winship, I Simonneau, G Galie, N Loyd, JE Humbert, M Nichols, WC Morrell, NW Berg, J Manes, A McGaughran, J Pauciulo, M Wheeler, L
Citation: Rc. Trembath et al., Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasia, N ENG J MED, 345(5), 2001, pp. 325-334
Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura
Authors: Levy, GG Nichols, WC Lian, EC Foroud, T McClintick, JN McGee, BM Yang, AY Siemieniak, DR Stark, KR Gruppo, R Sarode, R Shurin, SB Chandrasekaran, V Stabler, SP Sabio, H Bouhassira, EE Upshaw, JD Ginsburg, D Tsai, HM
Citation: Gg. Levy et al., Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura, NATURE, 413(6855), 2001, pp. 488-494
BMPR2 haploinsufficiency as the inherited molecular mechanism for primary pulmonary hypertension
Authors: Machado, RD Pauciulo, MW Thomson, JR Lane, KB Morgan, NV Wheeler, L Phillips, JA Newman, J Williams, D Galie, N Manes, A McNeil, K Yacoub, M Mikhail, G Rogers, P Corris, P Humbert, M Donnai, D Martensson, G Tranebjaerg, L Loyd, JE Trembath, RC Nichols, WC
Citation: Rd. Machado et al., BMPR2 haploinsufficiency as the inherited molecular mechanism for primary pulmonary hypertension, AM J HU GEN, 68(1), 2001, pp. 92-102
Heterozygous germline mutations in BMPR2, encoding a TGF-beta receptor, cause familial primary pulmonary hypertension
Authors: Lane, KB Machado, RD Pauciulo, MW Thomson, JR Phillips, JA Loyd, JE Nichols, WC Trembath, RC
Citation: Kb. Lane et al., Heterozygous germline mutations in BMPR2, encoding a TGF-beta receptor, cause familial primary pulmonary hypertension, NAT GENET, 26(1), 2000, pp. 81-84
A physical and transcript map based upon refinement of the critical interval for PPH1, a gene for familial primary pulmonary hypertension
Authors: Machado, RD Pauciulo, MW Fretwell, N Veal, C Thomson, JR Guell, CV Aldred, M Brannon, CA Trembath, RC Nichols, WC
Citation: Rd. Machado et al., A physical and transcript map based upon refinement of the critical interval for PPH1, a gene for familial primary pulmonary hypertension, GENOMICS, 68(2), 2000, pp. 220-228
Sporadic primary pulmonary hypertension is associated with germline mutations of the gene encoding BMPR-II, a receptor member of the TGF-beta family
Authors: Thomson, JR Machado, RD Pauciulo, MW Morgan, NV Humbert, M Elliott, GC Ward, K Yacoub, M Mikhail, G Rogers, P Newman, J Wheeler, L Higenbottam, T Gibbs, JSR Egan, J Crozier, A Peacock, A Allcock, R Corris, P Loyd, JE Trembath, RC Nichols, WC
Citation: Jr. Thomson et al., Sporadic primary pulmonary hypertension is associated with germline mutations of the gene encoding BMPR-II, a receptor member of the TGF-beta family, J MED GENET, 37(10), 2000, pp. 741-745
Integrative marital therapy
Authors: Nichols, WC
Citation: Wc. Nichols, Integrative marital therapy, SPR S COMPA, 2000, pp. 210-228
The molecular basis of von Willebrand disease
Authors: Mohlke, KL Nichols, WC Ginsburg, D
Citation: Kl. Mohlke et al., The molecular basis of von Willebrand disease, INT J CL L, 29(1), 1999, pp. 1-7
Mannose-dependent endoplasmic reticulum (ER)-Golgi intermediate compartment-53-mediated ER to Golgi trafficking of coagulation factors V and VIII
Authors: Moussalli, M Pipe, SW Hauri, HP Nichols, WC Ginsburg, D Kaufman, RJ
Citation: M. Moussalli et al., Mannose-dependent endoplasmic reticulum (ER)-Golgi intermediate compartment-53-mediated ER to Golgi trafficking of coagulation factors V and VIII, J BIOL CHEM, 274(46), 1999, pp. 32539-32542
Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V factor VIII deficiency
Authors: Neerman-Arbez, M Johnson, KM Morris, MA McVey, JH Peyvandi, F Nichols, WC Ginsburg, D Rossier, C Antonarakis, SE Tuddenham, EGD
Citation: M. Neerman-arbez et al., Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V factor VIII deficiency, BLOOD, 93(7), 1999, pp. 2253-2260
ERGIC-53 gene structure and mutation analysis in 19 combined factors V andVIII deficiency families
Authors: Nichols, WC Terry, VH Wheatley, MA Yang, A Zivelin, A Ciavarella, N Stefanile, C Matsushita, T Saito, H de Bosch, NB Ruiz-Saez, A Torres, A Thompson, AR Feinstein, DI White, GC Negrier, C Vinciguerra, C Aktan, M Kaufman, RJ Ginsburg, D Seligsohn, U
Citation: Wc. Nichols et al., ERGIC-53 gene structure and mutation analysis in 19 combined factors V andVIII deficiency families, BLOOD, 93(7), 1999, pp. 2261-2266
From the ER to the Golgi: Insights from the study of combined factors V and VIII deficiency
Authors: Nichols, WC Ginsburg, D
Citation: Wc. Nichols et D. Ginsburg, From the ER to the Golgi: Insights from the study of combined factors V and VIII deficiency, AM J HU GEN, 64(6), 1999, pp. 1493-1498
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