Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 20

1.

Complete genome sequence of Methanobacterium thermoautotrophicum deltaH: functional analysis and comparative genomics.

Smith DR, Doucette-Stamm LA, Deloughery C, Lee H, Dubois J, Aldredge T, Bashirzadeh R, Blakely D, Cook R, Gilbert K, Harrison D, Hoang L, Keagle P, Lumm W, Pothier B, Qiu D, Spadafora R, Vicaire R, Wang Y, Wierzbowski J, Gibson R, Jiwani N, Caruso A, Bush D, Reeve JN, et al.

J Bacteriol. 1997 Nov;179(22):7135-55.

2.

An insertional frameshift mutation of the beta-spectrin gene associated with elliptocytosis in spectrin nice (beta 220/216).

Tse WT, Gallagher PG, Pothier B, Costa FF, Scarpa A, Delaunay J, Forget BG.

Blood. 1991 Jul 15;78(2):517-23.

3.

Sp alpha V/41: a common spectrin polymorphism at the alpha IV-alpha V domain junction. Relevance to the expression level of hereditary elliptocytosis due to alpha-spectrin variants located in trans.

Alloisio N, Morlé L, Maréchal J, Roux AF, Ducluzeau MT, Guetarni D, Pothier B, Baklouti F, Ghanem A, Kastally R, Delaunay J, et al.

J Clin Invest. 1991 Jun;87(6):2169-77.

4.

Occurrence of the alpha I 22 Arg----His (CGT----CAT) spectrin mutation in Tunisia: potential association with severe elliptopoikilocytosis.

Baklouti F, Marechal J, Morle L, Alloisio N, Wilmotte R, Pothier B, Ducluzeau MT, Kastally R, Delaunay J.

Br J Haematol. 1991 May;78(1):108-13.

PMID:
2043465
5.

Exercise and arthritis. Kinesiology and the degenerative joint.

Pothier B, Allen ME.

Rheum Dis Clin North Am. 1990 Nov;16(4):989-1002. Review.

PMID:
2087588
6.

Two elliptocytogenic alpha I/74 variants of the spectrin alpha I domain. Spectrin Culoz (GGT----GTT; alpha I 40 Gly----Val) and spectrin Lyon (CTT----TTT; alpha I 43 Leu---Phe).

Morlé L, Roux AF, Alloisio N, Pothier B, Starck J, Denoroy L, Morlé F, Rudigoz RC, Forget BG, Delaunay J, et al.

J Clin Invest. 1990 Aug;86(2):548-54.

7.

A haemolytic syndrome associated with the complete absence of red cell membrane protein 4.2 in two Tunisian siblings.

Ghanem A, Pothier B, Marechal J, Ducluzeau MT, Morle L, Alloisio N, Feo C, Ben Abdeladhim A, Fattoum S, Delaunay J.

Br J Haematol. 1990 Jul;75(3):414-20.

PMID:
2386772
8.

Assignment of Sp alpha I/74 hereditary elliptocytosis to the alpha- or beta-chain of spectrin through in vitro dimer reconstitution.

Pothier B, Alloisio N, Maréchal J, Morlé L, Ducluzeau MT, Caldani C, Philippe N, Delaunay J.

Blood. 1990 May 15;75(10):2061-9.

9.

The red cell skeleton and its genetic disorders.

Delaunay J, Alloisio N, Morlé L, Pothier B.

Mol Aspects Med. 1990;11(3):161-241. Review. No abstract available.

PMID:
2403451
10.

Two distinct variants of erythrocyte spectrin beta IV domain.

Pothier B, Alloisio N, Morlé L, Maréchal J, Barthélemy H, Ducluzeau MT, Dorier A, Delaunay J.

Hum Genet. 1989 Nov;83(4):373-6.

PMID:
2807277
11.

Reduction of membrane band 7 and activation of volume stimulated (K+, Cl-)-cotransport in a case of congenital stomatocytosis.

Morlé L, Pothier B, Alloisio N, Féo C, Garay R, Bost M, Delaunay J.

Br J Haematol. 1989 Jan;71(1):141-6.

PMID:
2917122
12.

[Interaction between various alkylxanthines and the proteins of the erythrocyte skeleton].

Delaunay J, Pothier B, Baklouti F, Morlé L.

Pathol Biol (Paris). 1988 Oct;36(8 Pt 2):1076-80. French.

PMID:
3065699
13.

Spectrin Oran (alpha II/21), a new spectrin variant concerning the alpha II domain and causing severe elliptocytosis in the homozygous state.

Alloisio N, Morlé L, Pothier B, Roux AF, Maréchal J, Ducluzeau MT, Benhadji-Zouaoui Z, Delaunay J.

Blood. 1988 Apr;71(4):1039-47.

14.

Spectrin Tunis (alpha I/78): a new alpha I variant that causes asymptomatic hereditary elliptocytosis in the heterozygous state.

Morlé L, Alloisio N, Ducluzeau MT, Pothier B, Blibech R, Kastally R, Delaunay J.

Blood. 1988 Feb;71(2):508-11.

15.

Aberrant pattern of red cell membrane and cytosolic proteins in a case of congenital dyserythropoietic anaemia.

Pothier B, Morlé L, Alloisio N, Ducluzeau MT, Féo C, Blanchard D, Cartron JP, Garbarz M, Chaveroche I, Boivin P, et al.

Br J Haematol. 1987 Jul;66(3):393-400.

PMID:
3620358
16.

Spectrin Nice (beta 220/216): a shortened beta-chain variant associated with an increase of the alpha I/74 fragment in a case of elliptocytosis.

Pothier B, Morlé L, Alloisio N, Ducluzeau MT, Caldani C, Féo C, Garbarz M, Chaveroche I, Dhermy D, Lecomte MC, et al.

Blood. 1987 Jun;69(6):1759-65.

17.

Red cell membrane alteration involving protein 4.1 and protein 3 in a case of recessively inherited haemolytic anaemia.

Morlé L, Pothier B, Alloisio N, Ducluzeau MT, Marques S, Olim G, Martins e Silva J, Féo C, Garbarz M, Chaveroche I, et al.

Eur J Haematol. 1987 May;38(5):447-55.

PMID:
3653367
18.

Sp alpha I/65 hereditary elliptocytosis in North Africa.

Alloisio N, Guetarni D, Morlé L, Pothier B, Ducluzeau MT, Soun A, Colonna P, Clerc M, Philippe N, Delaunay J.

Am J Hematol. 1986 Oct;23(2):113-22.

PMID:
3752066
19.

Canada's Proposed CARE-MEDICO Project in Malaysia.

Pothier BE.

Can Med Assoc J. 1964 Jul 25;91(4):184. No abstract available.

20.

[Cardiac arrest in the operating room].

POTHIER B.

Union Med Can. 1959 Apr;88(4):434-7. French. No abstract available.

PMID:
13647700

Supplemental Content

Loading ...
Support Center