Similar articles for PMID: 8070816

Year	Number of Results
1985	2
1986	1
1988	2
1990	5
1991	7
1992	1
1993	9
1994	6
1995	17
1996	4
1997	6
1998	2
1999	11
2000	7
2001	2
2002	3
2003	2
2004	2
2005	2
2006	3
2007	2
2009	1
2010	3
2011	1
2012	1
2013	1
2016	1
2017	1
2022	1
2023	1
2024	0

1

MHC class II-deficient combined immunodeficiency: a disease of gene regulation.

Mach B, Steimle V, Reith W. Mach B, et al. Immunol Rev. 1994 Apr;138:207-21. doi: 10.1111/j.1600-065x.1994.tb00853.x. Immunol Rev. 1994. PMID: 8070816 Review. No abstract available.

2

Major histocompatibility complex class II deficiency: clinical manifestations, immunologic features, and outcome.

Klein C, Lisowska-Grospierre B, LeDeist F, Fischer A, Griscelli C. Klein C, et al. J Pediatr. 1993 Dec;123(6):921-8. doi: 10.1016/s0022-3476(05)80388-9. J Pediatr. 1993. PMID: 8229525

3

T cell differentiation and generation of the antigen-specific T cell repertoire in man: observations in MHC class II deficiency.

Mannhalter JW, Wolf HM, Hauber I, Miricka M, Gadner H, Eibl MM. Mannhalter JW, et al. Clin Exp Immunol. 1994 Sep;97(3):392-5. doi: 10.1111/j.1365-2249.1994.tb06100.x. Clin Exp Immunol. 1994. PMID: 8082293 Free PMC article.

4

Long-term survival of a urodele amphibian despite depleted major histocompatibility complex variation.

Babik W, Pabijan M, Arntzen JW, Cogâlniceanu D, Durka W, Radwan J. Babik W, et al. Mol Ecol. 2009 Mar;18(5):769-81. doi: 10.1111/j.1365-294X.2008.04057.x. Mol Ecol. 2009. PMID: 19207255

5

The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: evidence for a founder effect in the Moroccan population.

Naamane H, El Maataoui O, Ailal F, Barakat A, Bennani S, Najib J, Hassar M, Saile R, Bousfiha AA. Naamane H, et al. Eur J Pediatr. 2010 Sep;169(9):1069-74. doi: 10.1007/s00431-010-1179-6. Epub 2010 Apr 23. Eur J Pediatr. 2010. PMID: 20414676

6

Major histocompatibility complex class II deficiency: a disease of gene regulation.

Steimle V, Reith W, Mach B. Steimle V, et al. Adv Immunol. 1996;61:327-40. doi: 10.1016/s0065-2776(08)60870-6. Adv Immunol. 1996. PMID: 8834499 Review. No abstract available.

7

The bare lymphocyte syndrome: molecular clues to the transcriptional regulation of major histocompatibility complex class II genes.

DeSandro A, Nagarajan UM, Boss JM. DeSandro A, et al. Am J Hum Genet. 1999 Aug;65(2):279-86. doi: 10.1086/302519. Am J Hum Genet. 1999. PMID: 10417269 Free PMC article. Review. No abstract available.

8

Regulation of MHC class II genes: lessons from a disease.

Mach B, Steimle V, Martinez-Soria E, Reith W. Mach B, et al. Annu Rev Immunol. 1996;14:301-31. doi: 10.1146/annurev.immunol.14.1.301. Annu Rev Immunol. 1996. PMID: 8717517 Review.

9

RFXAP, a novel subunit of the RFX DNA binding complex is mutated in MHC class II deficiency.

Durand B, Sperisen P, Emery P, Barras E, Zufferey M, Mach B, Reith W. Durand B, et al. EMBO J. 1997 Mar 3;16(5):1045-55. doi: 10.1093/emboj/16.5.1045. EMBO J. 1997. PMID: 9118943 Free PMC article.

10

Genetic control of MHC class II expression.

Ting JP, Trowsdale J. Ting JP, et al. Cell. 2002 Apr;109 Suppl:S21-33. doi: 10.1016/s0092-8674(02)00696-7. Cell. 2002. PMID: 11983150 Free article. Review.

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