Pignata C - Search Results

1

FOXN1 in organ development and human diseases.

Palamaro L, Romano R, Fusco A, Giardino G, Gallo V, Pignata C. Palamaro L, et al. Among authors: pignata c. Int Rev Immunol. 2014 Mar;33(2):83-93. doi: 10.3109/08830185.2013.870171. Epub 2014 Jan 17. Int Rev Immunol. 2014. PMID: 24432845 Review.

2

Human equivalent of the mouse Nude/SCID phenotype: long-term evaluation of immunologic reconstitution after bone marrow transplantation.

Pignata C, Gaetaniello L, Masci AM, Frank J, Christiano A, Matrecano E, Racioppi L. Pignata C, et al. Blood. 2001 Feb 15;97(4):880-5. doi: 10.1182/blood.v97.4.880. Blood. 2001. PMID: 11159512 Free article.

3

Ancestral founder mutation of the nude (FOXN1) gene in congenital severe combined immunodeficiency associated with alopecia in southern Italy population.

Adriani M, Martinez-Mir A, Fusco F, Busiello R, Frank J, Telese S, Matrecano E, Ursini MV, Christiano AM, Pignata C. Adriani M, et al. Among authors: pignata c. Ann Hum Genet. 2004 May;68(Pt 3):265-8. doi: 10.1046/j.1529-8817.2004.00091.x. Ann Hum Genet. 2004. PMID: 15180707

4

FOXN1 homozygous mutation associated with anencephaly and severe neural tube defect in human athymic Nude/SCID fetus.

Amorosi S, D'Armiento M, Calcagno G, Russo I, Adriani M, Christiano AM, Weiner L, Brissette JL, Pignata C. Amorosi S, et al. Among authors: pignata c. Clin Genet. 2008 Apr;73(4):380-4. doi: 10.1111/j.1399-0004.2008.00977.x. Clin Genet. 2008. PMID: 18339010

5

The cellular amount of the common gamma-chain influences spontaneous or induced cell proliferation.

Amorosi S, Russo I, Amodio G, Garbi C, Vitiello L, Palamaro L, Adriani M, Vigliano I, Pignata C. Amorosi S, et al. Among authors: pignata c. J Immunol. 2009 Mar 1;182(5):3304-9. doi: 10.4049/jimmunol.0802400. J Immunol. 2009. PMID: 19234229

6

In ataxia-teleangiectasia betamethasone response is inversely correlated to cerebellar atrophy and directly to antioxidative capacity.

Russo I, Cosentino C, Del Giudice E, Broccoletti T, Amorosi S, Cirillo E, Aloj G, Fusco A, Costanzo V, Pignata C. Russo I, et al. Among authors: pignata c. Eur J Neurol. 2009 Jun;16(6):755-9. doi: 10.1111/j.1468-1331.2009.02600.x. Eur J Neurol. 2009. PMID: 19475758

7

Human clinical phenotype associated with FOXN1 mutations.

Pignata C, Fusco A, Amorosi S. Pignata C, et al. Adv Exp Med Biol. 2009;665:195-206. Adv Exp Med Biol. 2009. PMID: 20429426 Review.

8

Altered signaling through IL-12 receptor in children with very high serum IgE levels.

Fusco A, Vigliano I, Palamaro L, Cirillo E, Aloj G, Piscopo G, Giardino G, Pignata C. Fusco A, et al. Among authors: pignata c. Cell Immunol. 2010;265(1):74-9. doi: 10.1016/j.cellimm.2010.07.005. Epub 2010 Jul 21. Cell Immunol. 2010. PMID: 20696422

9

Efficacy of very-low-dose betamethasone on neurological symptoms in ataxia-telangiectasia.

Broccoletti T, Del Giudice E, Cirillo E, Vigliano I, Giardino G, Ginocchio VM, Bruscoli S, Riccardi C, Pignata C. Broccoletti T, et al. Among authors: pignata c. Eur J Neurol. 2011 Apr;18(4):564-70. doi: 10.1111/j.1468-1331.2010.03203.x. Epub 2010 Sep 14. Eur J Neurol. 2011. PMID: 20840352 Clinical Trial.

10

Brain alteration in a Nude/SCID fetus carrying FOXN1 homozygous mutation.

Amorosi S, Vigliano I, Del Giudice E, Panico L, Maruotti GM, Fusco A, Quarantelli M, Ciccone C, Ursini MV, Martinelli P, Pignata C. Amorosi S, et al. Among authors: pignata c. J Neurol Sci. 2010 Nov 15;298(1-2):121-3. doi: 10.1016/j.jns.2010.08.066. J Neurol Sci. 2010. PMID: 20864124

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