Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 152

1.

Comparative mapping of canine and human proximal Xq and genetic analysis of canine X-linked severe combined immunodeficiency.

Deschênes SM, Puck JM, Dutra AS, Somberg RL, Felsburg PJ, Henthorn PS.

Genomics. 1994 Sep 1;23(1):62-8.

PMID:
7829103
2.

IL-2R gamma gene microdeletion demonstrates that canine X-linked severe combined immunodeficiency is a homologue of the human disease.

Henthorn PS, Somberg RL, Fimiani VM, Puck JM, Patterson DF, Felsburg PJ.

Genomics. 1994 Sep 1;23(1):69-74.

PMID:
7829104
3.

The interleukin-2 receptor gamma chain maps to Xq13.1 and is mutated in X-linked severe combined immunodeficiency, SCIDX1.

Puck JM, Deschênes SM, Porter JC, Dutra AS, Brown CJ, Willard HF, Henthorn PS.

Hum Mol Genet. 1993 Aug;2(8):1099-104.

PMID:
8401490
4.
5.
6.

Physical and linkage mapping of human chromosome 17 loci to dog chromosomes 9 and 5.

Werner P, Raducha MG, Prociuk U, Henthorn PS, Patterson DF.

Genomics. 1997 May 15;42(1):74-82.

PMID:
9177778
7.

Transplantation of X-linked severe combined immunodeficient dogs with CD34+ bone marrow cells.

Hartnett BJ, Yao D, Suter SE, Ellinwood NM, Henthorn PS, Moore PE, McSweeney PA, Nash RA, Brown JD, Weinberg KI, Felsburg PJ.

Biol Blood Marrow Transplant. 2002;8(4):188-97.

8.

Missense mutation in exon 7 of the common gamma chain gene causes a moderate form of X-linked combined immunodeficiency.

Schmalstieg FC, Leonard WJ, Noguchi M, Berg M, Rudloff HE, Denney RM, Dave SK, Brooks EG, Goldman AS.

J Clin Invest. 1995 Mar;95(3):1169-73.

9.

Fine mapping of the human SCIDX1 locus at Xq12-13.1.

Markiewicz S, DiSanto JP, Chelly J, Fairweather N, Le Marec B, Griscelli C, Graeber MB, Müller U, Fischer A, Monaco AP, et al.

Hum Mol Genet. 1993 Jun;2(6):651-4.

PMID:
8353486
10.

Bone marrow transplantation for canine X-linked severe combined immunodeficiency.

Hartnett BJ, Henthorn PS, Moore PF, Weinberg KI, Ochs HD, Felsburg PJ.

Vet Immunol Immunopathol. 1999 Aug 2;69(2-4):137-44.

PMID:
10507301
11.
12.

Fine mapping of canine XLPRA establishes homology of the human and canine RP3 intervals.

Zhang Q, Acland GM, Zangerl B, Johnson JL, Mao Z, Zeiss CJ, Ostrander EA, Aguirre GD.

Invest Ophthalmol Vis Sci. 2001 Oct;42(11):2466-71.

PMID:
11581184
14.

Trisomy X in a female member of a family with X linked severe combined immunodeficiency: implications for carrier diagnosis.

Lester T, de Alwis M, Clark PA, Jones AM, Katz F, Levinsky RJ, Kinnon C.

J Med Genet. 1994 Sep;31(9):717-20.

15.

Mapping of X-linked progressive retinal atrophy (XLPRA), the canine homolog of retinitis pigmentosa 3 (RP3).

Zeiss CJ, Ray K, Acland GM, Aguirre GD.

Hum Mol Genet. 2000 Mar 1;9(4):531-7.

PMID:
10699176
16.

Characterization of the canine desmin (DES) gene and evaluation as a candidate gene for dilated cardiomyopathy in the Dobermann.

Stabej P, Imholz S, Versteeg SA, Zijlstra C, Stokhof AA, Domanjko-Petric A, Leegwater PA, van Oost BA.

Gene. 2004 Oct 13;340(2):241-9.

PMID:
15475165
17.

X chromosome linked immunodeficiency.

Schwaber J, Rosen FS.

Immunodefic Rev. 1990;2(3):233-51. Review.

PMID:
1981831
18.
19.

Carrier identification in X-linked immunodeficiency diseases.

Li SL, Ting SS, Lindeman R, Ffrench R, Ziegler JB.

J Paediatr Child Health. 1998 Jun;34(3):273-9.

PMID:
9633977
20.

Alport syndrome. Molecular genetic aspects.

Hertz JM.

Dan Med Bull. 2009 Aug;56(3):105-52.

PMID:
19728970

Supplemental Content

Support Center