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Pacing and Clinical Electrophysiology : PACE|February 6, 2013
Differences in clinical and echocardiographic parameters between paroxysmal and persistent atrial flutter in the AURUM 8 study: targets for prevention of persistent arrhythmia?Lars Lickfett, Erica Mittmann-Braun, Christian Weiss, et al.
Plant, Cell & Environment|October 18, 2018
Modelling predicts that soybean is poised to dominate crop production across AfricaChristine H Foyer, Kadambot H M Siddique, Amos P K Tai, et al.
The Journal of Allergy and Clinical Immunology|June 23, 2022
Art v 1 IgE epitopes of patients and humanized mice are conformationalMaja Zabel, Milena Weber, Bernhard Kratzer, et al.
Eclinicalmedicine|February 8, 2021
Nocturnal respiratory rate predicts ICD benefit: A prospective, controlled, multicentre cohort studyMichael Dommasch, Alexander Steger, Petra Barthel, et al.
JCI Insight|February 8, 2019
Hypomorphic mutations of TRIP11 cause odontochondrodysplasiaAnika Wehrle, Tomasz M Witkos, Sheila Unger, et al.
American Journal of Medical Genetics. Part A|April 14, 2007
Ovotestes and XY sex reversal in a female with an interstitial 9q33.3-q34.1 deletion encompassing NR5A1 and LMX1B causing features of Genitopatellar syndromeSilke Schlaubitz, Svetlana A Yatsenko, Laurie D Smith, et al.
Theriogenology|August 27, 2018
Expression pattern of new genes regulating female sex differentiation and in vitro maturational status of oocytes in pigsKatarzyna Ożegowska, Marta Dyszkiewicz-Konwińska, Piotr Celichowski, et al.
The Journal of Experimental Medicine|November 2, 1999
Human G protein-coupled receptor GPR-9-6/CC chemokine receptor 9 is selectively expressed on intestinal homing T lymphocytes, mucosal lymphocytes, and thymocytes and is required for thymus-expressed chemokine-mediated chemotaxisB A Zabel, W W Agace, J J Campbell, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 9, 2010
Osteopathia striata with cranial sclerosis owing to WTX gene defectBram Perdu, Fenna de Freitas, Suzanne G M Frints, et al.
Nature Genetics|February 26, 2008
Mutations in the cyclin family member FAM58A cause an X-linked dominant disorder characterized by syndactyly, telecanthus and anogenital and renal malformationsSheila Unger, Detlef Böhm, Frank J Kaiser, et al.
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