Publications by authors named "Lana Strmecki"

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Releasing Activity Disengages Cohesin's Smc3/Scc1 Interface in a Process Blocked by Acetylation.
Frederic Beckouët, Madhusudhan Srinivasan, Maurici Brunet Roig, Kok-Lung Chan, Johanna C Scheinost, Lana Strmecki

Mol Cell· February 2016

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De novo mutation in DMD gene in a patient with combined hemophilia A and Duchenne muscular dystrophy.
Lana Strmecki, Petra Hudler, Majda Benedik-Dolničar, Radovan Komel

Int J Hematol· February 2014

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A positively charged channel within the Smc1/Smc3 hinge required for sister chromatid cohesion.
Alexander Kurze, Katharine A Michie, Sarah E Dixon, Ajay Mishra, Takehiko Itoh, Lana Strmecki

EMBO J· January 2011

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Proteomic and microarray analyses of the Dictyostelium Zak1-GSK-3 signaling pathway reveal a role in early development.
Lana Strmecki, Gareth Bloomfield, Tsuyoshi Araki, Emma Dalton, Jason Skelton

Eukaryot Cell· February 2007

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PKD1 and PKD2 mutations in Slovenian families with autosomal dominant polycystic kidney disease.
Katja Vouk, Lana Strmecki, Jitka Stekrova, Jana Reiterova, Matjaz Bidovec

BMC Med Genet· January 2006

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Developmental decisions in Dictyostelium discoideum.
Lana Strmecki, David M Greene, Catherine J Pears

Dev Biol· August 2005

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Haemophilia A and mucopolysaccharidosis I-H (Hurler Syndrome): a case report.
Majda Benedik-Dolnicar, Lana Strmecki, Eduard Paschke, Cordula Steglich, Olga Kranjc

Haematologica· August 2002

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The position of the polycystic kidney disease 1 (PKD1) gene mutation correlates with the severity of renal disease.
Sandro Rossetti, Sarah Burton, Lana Strmecki, Gregory R Pond, Jośe L San Millán

J Am Soc Nephrol· May 2002

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Mutational analysis of 30 Slovenian cystic fibrosis patients compared to known Slovenian and European CF mutation spectra.
Katja Vouk, Lana Strmecki, Mirjana Liovic, Silvester Kopriva, Dusica Micetic-Turk

Pflugers Arch· January 2000

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