Results
|
221.
|
Leukocyte Adhesion Deficiency Type II is a generalized defect of de novo GDP-fucose biosynthesis. Endothelial cell fucosylation is not required for neutrophil rolling on human nonlymphoid endothelium. [electronic resource] by
- Karsan, A
- Cornejo, C J
- Winn, R K
- Schwartz, B R
- Way, W
- Lannir, N
- Gershoni-Baruch, R
- Etzioni, A
- Ochs, H D
- Harlan, J M
Producer: 19980626
In:
The Journal of clinical investigation vol. 101
Availability: No items available.
|
|
222.
|
Genetic and molecular definition of complementation group D in MHC class II deficiency. [electronic resource] by
- Fondaneche, M C
- Villard, J
- Wiszniewski, W
- Jouanguy, E
- Etzioni, A
- Le Deist, F
- Peijnenburg, A
- Casanova, J L
- Reith, W
- Mach, B
- Fischer, A
- Lisowska-Grospierre, B
Producer: 19980826
In:
Human molecular genetics vol. 7
Availability: No items available.
|
|
223.
|
Primary immunodeficiency mutation databases. [electronic resource] by
- Vihinen, M
- Arredondo-Vega, F X
- Casanova, J L
- Etzioni, A
- Giliani, S
- Hammarström, L
- Hershfield, M S
- Heyworth, P G
- Hsu, A P
- Lähdesmäki, A
- Lappalainen, I
- Notarangelo, L D
- Puck, J M
- Reith, W
- Roos, D
- Schumacher, R F
- Schwarz, K
- Vezzoni, P
- Villa, A
- Väliaho, J
- Smith, C I
Producer: 20010208
In:
Advances in genetics vol. 43
Availability: No items available.
|
|
224.
|
Clinical spectrum of X-linked hyper-IgM syndrome. [electronic resource] by
- Levy, J
- Espanol-Boren, T
- Thomas, C
- Fischer, A
- Tovo, P
- Bordigoni, P
- Resnick, I
- Fasth, A
- Baer, M
- Gomez, L
- Sanders, E A
- Tabone, M D
- Plantaz, D
- Etzioni, A
- Monafo, V
- Abinun, M
- Hammarstrom, L
- Abrahamsen, T
- Jones, A
- Finn, A
- Klemola, T
- DeVries, E
- Sanal, O
- Peitsch, M C
- Notarangelo, L D
Producer: 19970904
In:
The Journal of pediatrics vol. 131
Availability: No items available.
|
|
225.
|
The mutational spectrum of human malignant autosomal recessive osteopetrosis. [electronic resource] by
- Sobacchi, C
- Frattini, A
- Orchard, P
- Porras, O
- Tezcan, I
- Andolina, M
- Babul-Hirji, R
- Baric, I
- Canham, N
- Chitayat, D
- Dupuis-Girod, S
- Ellis, I
- Etzioni, A
- Fasth, A
- Fisher, A
- Gerritsen, B
- Gulino, V
- Horwitz, E
- Klamroth, V
- Lanino, E
- Mirolo, M
- Musio, A
- Matthijs, G
- Nonomaya, S
- Notarangelo, L D
- Ochs, H D
- Superti Furga, A
- Valiaho, J
- van Hove, J L
- Vihinen, M
- Vujic, D
- Vezzoni, P
- Villa, A
Producer: 20020115
In:
Human molecular genetics vol. 10
Availability: No items available.
|
|
226.
|
CD40lbase: a database of CD40L gene mutations causing X-linked hyper-IgM syndrome. [electronic resource] by
- Notarangelo, L D
- Peitsch, M C
- Abrahamsen, T G
- Bachelot, C
- Bordigoni, P
- Cant, A J
- Chapel, H
- Clementi, M
- Deacock, S
- de Saint Basile, G
- Duse, M
- Espanol, T
- Etzioni, A
- Fasth, A
- Fischer, A
- Giliani, S
- Gomez, L
- Hammarstorm, L
- Jones, A
- Kanariou, M
- Kinnon, C
- Klemola, T
- Kroczek, R A
- Levy, J
- Matamoros, N
- Monafo, V
- Paolucci, P
- Reznick, I
- Sanal, O
- Smith, C I
- Thompson, R A
- Tovo, P
- Villa, A
- Vihinen, M
- Vossen, J
- Zegers, B J
Producer: 19970206
In:
Immunology today vol. 17
Availability: No items available.
|