Publications by authors named "Stephan Tanner"

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Use of modern magnetic resonance imaging technology for lumbar screw planning.
Yorck Rommelspacher, Andrew Dixon, André Pascal Schulte, Stephan Tanner, Frank Schellhammer

Brain Spine· December 2025

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Evaluation of MRI technologies for surgical spine planning and navigation.
Yorck Rommelspacher, André Pascal Schulte, Stephan Tanner, Frank Schellhammer, Sabine Kling

Eur Spine J· April 2025

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Current updates in radiocontrast-associated acute kidney injury.
Mohammed Mahgoub, Jerry Fan, Luis Concepcion, Stephan B Tanner, Kadilee Adams

Proc (Bayl Univ Med Cent)· August 2024

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Human iPSC-derived iMSCs improve bone regeneration in mini-pigs.
Pascal Jungbluth, Lucas-Sebastian Spitzhorn, Jan Grassmann, Stephan Tanner, David Latz

Bone Res· October 2019

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Is computerised 3D templating more accurate than 2D templating to predict size of components in primary total hip arthroplasty?
Erik Schiffner, David Latz, Pascal Jungbluth, Jan P Grassmann, Stephan Tanner

Hip Int· May 2019

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Germline allele-specific expression of DAPK1 in chronic lymphocytic leukemia.
Quan-Xiang Wei, Rainer Claus, Thomas Hielscher, Daniel Mertens, Aparna Raval, Stephan M Tanner

PLoS One· July 2013

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Hereditary intrinsic factor deficiency in chaldeans.
Amy C Sturm, Elizabeth C Baack, Michael B Armstrong, Deborah Schiff, Ayesha Zia, Stephan M Tanner

JIMD Rep· February 2013

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Acute lymphoblastic leukemia and vitamin B12 deficiency secondary to a gastric intrinsic factor gene mutation.
Ayesha Zia, Tunç Fışgin, Catherine Sokolowski, Stephan M Tanner, Süreyya Savaşan

Pediatr Blood Cancer· October 2012

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Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns.
Stephan M Tanner, Amy C Sturm, Elizabeth C Baack, Sandya Liyanarachchi, Albert de la Chapelle

Orphanet J Rare Dis· August 2012

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miR-3151 interplays with its host gene BAALC and independently affects outcome of patients with cytogenetically normal acute myeloid leukemia.
Ann-Kathrin Eisfeld, Guido Marcucci, Kati Maharry, Sebastian Schwind, Michael D Radmacher, Stephan M Tanner

Blood· July 2012

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Imerslund-Gräsbeck syndrome: new mutation in amnionless.
Narumon Densupsoontorn, Kleebsabai Sanpakit, Chodchanok Vijarnsorn, Aniruth Pattaragarn, Channagarn Kangwanpornsiri, Stephan M Tanner

Pediatr Int· June 2012

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Heritable polymorphism predisposes to high BAALC expression in acute myeloid leukemia.
Ann-Kathrin Eisfeld, Guido Marcucci, Sandya Liyanarachchi, Konstanze Döhner, Sebastian Schwind, Stephan M Tanner

Proc Natl Acad Sci U S A· April 2012

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Juvenile cobalamin deficiency in a 17-year-old child with autonomic dysfunction and skin changes.
Abdul Hafeez Siddiqui, Aamir Ansari, Cameron M Beech, Nidhi P Shah, Stephan M Tanner

J Pediatr Hematol Oncol· March 2012

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Familial peripheral keratopathy without PAX6 mutation.
Wendy M Smith, Julie M Lange, Amy C Sturm, Stephan M Tanner, Thomas F Mauger

Cornea· February 2012

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Variants in the netrin-1 receptor UNC5C prevent apoptosis and increase risk of familial colorectal cancer.
Marie-May Coissieux, Jerneja Tomsic, Marie Castets, Heather Hampel, Sari Tuupanen, Stephan M Tanner

Gastroenterology· December 2011

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Ancient founder mutation is responsible for Imerslund-Gräsbeck Syndrome among diverse ethnicities.
Cameron M Beech, Sandya Liyanarachchi, Nidhi P Shah, Amy C Sturm, May F Sadiq, Stephan M Tanner

Orphanet J Rare Dis· November 2011

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Juvenile selective vitamin B₁₂ malabsorption: 50 years after its description-10 years of genetic testing.
Ralph Gräsbeck, Stephan M Tanner

Pediatr Res· September 2011

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[Homozygous mutation in the intrinsic factor gene in a child with severe vitamin B12 deficiency].
Tina Lund Leunbach, Preben Johansen, Stephan M Tanner, Ralph Gräsbeck, Jon Helgestad

Ugeskr Laeger· August 2011

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Investigation of the ABC transporter MRP1 in selected patients with presumed defects in vitamin B12 absorption.
Nidhi P Shah, Cameron M Beech, Amy C Sturm, Stephan M Tanner

Blood· April 2011

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Allele-specific expression of TGFBR1 in colon cancer patients.
Jerneja Tomsic, Kishore Guda, Sandya Liyanarachchi, Heather Hampel, Leanna Natale, Stephan M Tanner

Carcinogenesis· October 2010

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Epigallocatechin gallate-induced modulation of FoxO signaling in mammalian cells and C. elegans: FoxO stimulation is masked via PI3K/Akt activation by hydrogen peroxide formed in cell culture.
André Bartholome, Andreas Kampkötter, Stephan Tanner, Helmut Sies, Lars-Oliver Klotz

Arch Biochem Biophys· September 2010

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Vitamin B12 deficiency in a 15-year old boy due to mutations in the intrinsic factor gene, GIF.
Ulrik M Overgaard, Stephan M Tanner, Henrik S Birgens

Br J Haematol· August 2010

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RelA/p65 functions to maintain cellular senescence by regulating genomic stability and DNA repair.
Jingxin Wang, Naduparambil K Jacob, Katherine J Ladner, Amer Beg, James D Perko, Stephan M Tanner

EMBO Rep· November 2009

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Infrequent detection of germline allele-specific expression of TGFBR1 in lymphoblasts and tissues of colon cancer patients.
Kishore Guda, Leanna Natale, James Lutterbaugh, Georgia L Wiesner, Susan Lewis, Stephan M Tanner

Cancer Res· June 2009

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Juvenile cobalamin deficiency in individuals of African ancestry is caused by a founder mutation in the intrinsic factor gene GIF.
Andrea E Ament, Zhongyuan Li, Amy C Sturm, James D Perko, Sarah Lawson, Stephan M Tanner

Br J Haematol· February 2009

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