Browse by UCL Departments and Centres
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Group by: Author | Type
Number of items: 21.
A
| ALTERMAN, LA and DEALWIS, M and GENET, S and LOVERING, R and MIDDLETONPRICE, H and MORGAN, G and JONES, A and MALCOLM, S and LEVINSKY, RJ and KINNON, C (1993) CARRIER DETERMINATION FOR X-LINKED AGAMMAGLOBULINEMIA USING X-INACTIVATION ANALYSIS OF PURIFIED B-CELLS. J IMMUNOL METHODS , 166 (1) 111 - 116. |
| Alton, EWFE and Middleton, PG and Caplen, NJ and Smith, SN and Steel, DM and Munkonge, FM and Jeffrey, PK and Geddes, DM and Hart, SL and Williamson, R and Fasold, KI and Miller, AD and Dickinson, P and Stevenson, BJ and McLachlan, G and Dorin, JR (1993) Non-invasive liposome-mediated gene delivery can correct the ion transport defect in cystic fibrosis mutant mice. Nature Genetics , 5 135 - 142. |
G
| Gustafsson, K and Germana, S and Sundt, TM and Sachs, DH and LeGuern, C (1993) Extensive allelic polymorphism in the CDR2-like region of the miniature swine CD4 molecule. J Immunol , 151 (3) 1365 - 1370. |
| Gustafsson, K and Rask, L and Andersson, L (1993) Structure of porcine MHC class II DRB genes. Immunogenetics , 37 (4) 312 - 314. |
H
| Holmdahl, R and Karlsson, M and Gustafsson, K and Hedrich, H (1993) Structural polymorphism of six rat RT1Ba genes. Immunogenetics , 38 (5) 381 - ?. |
J
| Jones, A and Morris, T and de Alwis, M and Malcolm, S and Levinsky, RJ and Kinnon, C (1993) Physical and genetic mapping in the region of Xq12-21, which contains the locus for X-linked severe combined immunodeficiency. Immunodeficiency , 4 (1-4) 259 - 262. |
| JONES, AM and MALCOLM, S and LEVINSKY, RJ and KINNON, C (1993) PHYSICAL MAPPING IN THE REGION OF HUMAN XQ12-21.1 USING PULSED-FIELD GEL-ELECTROPHORESIS. HUM GENET , 91 (5) 485 - 488. |
K
| KINNON, C and HINSHELWOOD, S and LEVINSKY, RJ and LOVERING, RC (1993) X-LINKED AGAMMAGLOBULINEMIA - GENE CLONING AND FUTURE-PROSPECTS. IMMUNOL TODAY , 14 (11) 554 - 558. |
| KINNON, C and OREILLY, MA and SWEATMAN, A and BRADLEY, L and ALTERMAN, L and LOVERING, R and MALCOLM, S and LEVINSKY, R (1993) PHYSICAL APPROACHES TO THE ISOLATION OF THE X-LINKED AGAMMAGLOBULINEMIA GENE (XLA). J CELL BIOCHEM 165 - 165. |
L
| LEVINSKY, RJ and PARKAR, MH and COLLINS, MKL and KINNON, C and PORTER, CD (1993) X-LINKED CHRONIC GRANULOMATOUS-DISEASE - CORRECTION OF NADPH OXIDASE DEFECTS BY RETROVIRUS-MEDIATED GENE-TRANSFER. J CELL BIOCHEM 232 - 232. |
| LOVERING, R and MIDDLETONPRICE, HR and OREILLY, MAJ and GENET, SA and PARKAR, M and SWEATMAN, AK and BRADLEY, LD and ALTERMAN, LA and MALCOLM, S and MORGAN, G and LEVINSKY, RJ and KINNON, C (1993) GENETIC-LINKAGE ANALYSIS IDENTIFIES NEW PROXIMAL AND DISTAL FLANKING MARKERS FOR THE X-LINKED AGAMMAGLOBULINEMIA GENE LOCUS, REFINING ITS LOCALIZATION IN XQ22. HUM MOL GENET , 2 (2) 139 - 141. |
| LOVERING, R and PADAYACHEE, M and OREILLY, MA and MIDDLETONPRICE, H and GENET, S and PARKAR, M and ALTERMAN, L and SWEATMAN, A and BRADLEY, L and MALCOLM, S and LEVINSKY, R and KINNON, C (1993) GENETIC-LINKAGE ANALYSIS FOR X-LINKED AGAMMAGLOBULINEMIA (XLA) AND X-LINKED HYPER IGM (XHM). J CELL BIOCHEM 182 - 182. |
| LOVERING, R and SWEATMAN, AK and OREILLY, MAJ and GENET, SA and MIDDLETONPRICE, H and MALCOLM, S and LEVINSKY, RJ and KINNON, C (1993) PHYSICAL MAPPING IDENTIFIES DXS265 AS A USEFUL GENETIC-MARKER FOR CARRIER DETECTION AND PRENATAL-DIAGNOSIS OF X-LINKED AGAMMAGLOBULINEMIA. HUM GENET , 91 (2) 178 - 180. |
M
| Mattsson, R and Mattson, A and Brunsberg, U and Holmdahl, R and Gustafsson, K (1993) Tansgenic MHC class II A mouse model of potential interest for studies of antifetal immune rections. J.Immunol. , 151 1365 - 1370. |
O
| OREILLY, MAJ and ALTERMAN, LA and ZIJLSTRA, J and MALCOLM, S and LEVINSKY, RJ and KINNON, C (1993) PULSED-FIELD GEL-ELECTROPHORESIS AND RADIATION HYBRID MAPPING ANALYSES ENABLE THE ORDERING OF 11 DNA LOCI IN XQ22. GENOMICS , 15 (2) 275 - 282. |
| OREILLY, MAJ and SWEATMAN, AK and BRADLEY, LD and ALTERMAN, LA and LOVERING, R and MALCOLM, S and LEVINSKY, RJ and KINNON, C (1993) ISOLATION AND MAPPING OF DISCRETE DXS101 LOCI IN XQ22 NEAR THE X-LINKED AGAMMAGLOBULINEMIA GENE LOCUS. HUM GENET , 91 (6) 605 - 608. |
P
| PADAYACHEE, M and LEVINSKY, RJ and KINNON, C and FINN, A and MCKEOWN, C and FEIGHERY, C and NOTARANGELO, LD and HENDRIKS, RW and READ, AP and MALCOLM, S (1993) MAPPING OF THE X-LINKED FORM OF HYPER-IGM SYNDROME (HIGM1). J MED GENET , 30 (3) 202 - 205. |
| PORTER, CD and PARKAR, MH and LEVINSKY, RJ and COLLINS, MKL and KINNON, C (1993) X-LINKED CHRONIC GRANULOMATOUS-DISEASE - CORRECTION OF NADPH OXIDASE DEFECT BY RETROVIRUS-MEDIATED EXPRESSION OF GP91-PHOX. BLOOD , 82 (7) 2196 - 2202. |
S
| SWEATMAN, A and LOVERING, R and MIDDLETONPRICE, H and JONES, A and MORGAN, G and LEVINSKY, R and KINNON, C (1993) A NEW RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM AT THE DXS101 LOCUS ALLOWS CARRIER DETECTION IN A FAMILY WITH X-LINKED AGAMMAGLOBULINEMIA. J MED GENET , 30 (6) 512 - 514. |
T
| Thrasher, A and Segal, A and Casimir, C (1993) Chronic granulomatous disease: towards gene therapy. Immunodeficiency , 4 (1-4) 327 - 333. |
V
| VETRIE, D and VORECHOVSKY, I and SIDERAS, P and HOLLAND, J and DAVIES, A and FLINTER, F and HAMMARSTROM, L and KINNON, C and LEVINSKY, R and BOBROW, M and SMITH, CIE and BENTLEY, DR (1993) THE GENE INVOLVED IN X-LINKED AGAMMAGLOBULINEMIA IS A MEMBER OF THE SRC FAMILY OF PROTEIN-TYROSINE KINASES. NATURE , 361 (6409) 226 - 233. |


