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Items: 8

1.

XIAP controls RIPK2 signaling by preventing its deposition in speck-like structures.

Ellwanger K, Briese S, Arnold C, Kienes I, Heim V, Nachbur U, Kufer TA.

Life Sci Alliance. 2019 Jul 26;2(4). pii: e201900346. doi: 10.26508/lsa.201900346. Print 2019 Aug.

2.

A hospital-based intermittent nocturnal hemodialysis program for children and adolescents.

Hoppe A, von Puttkamer C, Linke U, Kahler C, Booss M, Braunauer-Kolberg R, Hofmann K, Joachimsky P, Hirte I, Schley S, Utsch B, Thumfart J, Briese S, Gellermann J, Zimmering M, Querfeld U, Müller D.

J Pediatr. 2011 Jan;158(1):95-9, 99.e1. doi: 10.1016/j.jpeds.2010.06.036. Epub 2010 Aug 9.

PMID:
20691454
3.

Arterial stiffness in children after renal transplantation.

Briese S, Claus M, Querfeld U.

Pediatr Nephrol. 2008 Dec;23(12):2241-5. doi: 10.1007/s00467-008-0894-y. Epub 2008 Jun 27.

PMID:
18584211
4.

Endocytosis of the glucose transporter GLUT8 is mediated by interaction of a dileucine motif with the beta2-adaptin subunit of the AP-2 adaptor complex.

Schmidt U, Briese S, Leicht K, Schürmann A, Joost HG, Al-Hasani H.

J Cell Sci. 2006 Jun 1;119(Pt 11):2321-31.

5.

Arterial and cardiac disease in young adults with childhood-onset end-stage renal disease-impact of calcium and vitamin D therapy.

Briese S, Wiesner S, Will JC, Lembcke A, Opgen-Rhein B, Nissel R, Wernecke KD, Andreae J, Haffner D, Querfeld U.

Nephrol Dial Transplant. 2006 Jul;21(7):1906-14. Epub 2006 Mar 22.

PMID:
16554325
6.

Two familial cases with tumor necrosis factor receptor-associated periodic syndrome caused by a non-cysteine mutation (T50M) in the TNFRSF1A gene associated with severe multiorganic amyloidosis.

Kallinich T, Briese S, Roesler J, Rudolph B, Sarioglu N, Blankenstein O, Keitzer R, Querfeld U, Haffner D.

J Rheumatol. 2004 Dec;31(12):2519-22.

PMID:
15570662
7.

Post-transplantation swelling of the lower eyelid.

Koenig K, Briese S, Wiemann D, Haffner D, Querfeld U.

Nephrol Dial Transplant. 2004 Apr;19(4):1001-3. No abstract available.

PMID:
15031366
8.

A gene locus for steroid-resistant nephrotic syndrome with deafness maps to chromosome 14q24.2.

Ruf RG, Wolf MT, Hennies HC, Lucke B, Zinn C, Varnholt V, Lichtenberger A, Pasch A, Imm A, Briese S, Lennert T, Fuchshuber A, Nurnberg P, Hildebrandt F.

J Am Soc Nephrol. 2003 Jun;14(6):1519-22.

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