| | Title | Authors / Editors | Date |
|
unige:10898 |
An MRL/MpJ-lpr/lpr substrain with a limited expansion of lpr double-negative T cells and a reduced autoimmune syndrome |
Fossati-Jimack, Liliane; Takahashi, Satoru; Merino, Ramon; Iwamoto, Masahiro; ... Izui, Shozo |
1993 |
|
unige:161989 |
Carboxypeptidase A6 gene (CPA6) mutations in a recessive familial form of febrile seizures and temporal lobe epilepsy and in sporadic temporal lobe epilepsy |
Salzmann, Annick; Guipponi, Michel; Lyons, Peter J; Fricker, Lloyd D; ... Malafosse, Alain |
2012 |
|
unige:160563 |
Cas9-mediated allelic exchange repairs compound heterozygous recessive mutations in mice |
Wang, Dan; Li, Jia; Song, Chun-Qing; Tran, Karen; ... Gao, Guangping |
2018 |
|
unige:160765 |
Chorea-Acanthocytosis: genetic linkage to chromosome 9q21 |
Rubio, Justin P.; Danek, Adrian; Stone, Caroline; Chalmers, Richard; ... Monaco, Anthony P. |
1997 |
|
unige:11214 |
Functional analysis of T cell subsets from mice bearing the lpr gene |
Davignon, J. L.; Budd, R. C.; Ceredig, R.; Piguet, P. F.; ... Izui, Shozo |
1985 |
|
unige:10918 |
IgG rheumatoid factors and cryoglobulins in mice bearing the mutant gene lpr (lymphoproliferation) |
Izui, Shozo; Abdelmoula, M.; Gyotoku, Y.; Lange, G.; Lambert, Paul Henri |
1984 |
|
unige:11347 |
Induction of various autoantibodies by mutant gene lpr in several strains of mice |
Izui, Shozo; Kelley, V. E.; Masuda, K.; Yoshida, Haruyoshi; ... Murphy, E. D. |
1984 |
|
unige:76385 |
Infectious disease. Life-threatening influenza and impaired interferon amplification in human IRF7 deficiency |
Ciancanelli, Michael J; Huang, Sarah X L; Luthra, Priya; Garner, Hannah; ... Casanova, Jean-Laurent |
2015 |
|
unige:8935 |
Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V-factor VIII deficiency |
Neerman Arbez, Marguerite; Johnson, K. M.; Morris, Michael Andréw; McVey, J. H.; ... Tuddenham, E. G. |
1999 |
|
unige:8638 |
Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness |
Ben-Yosef, T.; Wattenhofer, M.; Riazuddin, S.; Ahmed, Z. M.; ... Morell, R. J. |
2001 |
|
unige:8937 |
Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family |
Neerman Arbez, Marguerite; Vu, Dung; Abu-Libdeh, Bassam; Bouchardy, Isabelle; Morris, Michael Andréw |
2003 |
|
unige:77288 |
Recessive thrombocytopenia likely due to a homozygous pathogenic variant in the FYB gene: case report |
Al Hamami, Hanan; Makrythanasis, Periklis; Al-Allawi, Nasir; Muhsin, Abdulrahman A; Antonarakis, Stylianos |
2014 |
|
unige:9259 |
Refined genetic mapping of the autosomal recessive non-syndromic deafness locus DFNB8 on human chromosome 21q22.3 |
Scott, Hamish Steele; Antonarakis, Stylianos; Mittaz, L.; Lalioti, M. D.; ... Gal, A. |
2000 |
|
unige:8639 |
Refined localization of autosomal recessive nonsyndromic deafness DFNB10 locus using 34 novel microsatellite markers, genomic structure, and exclusion of six known genes in the region |
Berry, A.; Scott, Hamish Steele; Kudoh, J.; Talior, I.; ... Bonne-Tamir, B. |
2000 |
|
unige:11348 |
Resistance to tolerance induction is not prerequisite to development of murine SLE |
Izui, Shozo; Masuda, K. |
1984 |
|
unige:11544 |
The bare lymphocyte syndrome and the regulation of MHC expression |
Reith, Walter; Mach, Bernard |
2001 |
|
unige:1279 |
TMPRSS3, a type II transmembrane serine protease mutated in non-syndromic autosomal recessive deafness |
Guipponi, Michel; Antonarakis, Stylianos; Scott, Hamish Steele |
2008 |
Genes, recessive
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