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Gudrun A Rappold

Showing results (51-60 of 77) with videos related to

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Hormone Research in Paediatrics|May 14, 2015
Radiological Features in Patients with Short Stature Homeobox-Containing (SHOX) Gene Deficiency and Turner Syndrome before and after 2 Years of GH TreatmentChristopher J Child, Gabriel Kalifa, Christine Jones, et al.
Human Molecular Genetics|December 10, 2015
Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorderElliot Sollis, Sarah A Graham, Arianna Vino, et al.
Frontiers in Endocrinology|July 1, 2021
Evidence That Non-Syndromic Familial Tall Stature Has an Oligogenic Origin Including Ciliary GenesBirgit Weiss, Birgit Eberle, Ralph Roeth, et al.
The Journal of Biological Chemistry|May 18, 2004
The short stature homeodomain protein SHOX induces cellular growth arrest and apoptosis and is expressed in human growth plate chondrocytesAntonio Marchini, Tiina Marttila, Anja Winter, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2017
Identification of SLC20A1 and SLC15A4 among other genes as potential risk factors for combined pituitary hormone deficiencyFranziska Simm, Anne Griesbeck, Daniela Choukair, et al.
Molecular Psychiatry|May 22, 2021
Imbalanced post- and extrasynaptic SHANK2A functions during development affect social behavior in SHANK2-mediated neuropsychiatric disordersAhmed Eltokhi, Miguel A Gonzalez-Lozano, Lars-Lennart Oettl, et al.
Journal of the American Heart Association|January 22, 2026
<i>CAV1</i>-A Susceptibility Gene for Atrial Fibrillation: The Impact of Coding and Noncoding VariantsKristin Rädecke, David Rheinert, Annette Löwen, et al.
Molecular Psychiatry|July 8, 2021
Correction: Imbalanced post- and extrasynaptic SHANK2A functions during development affect social behavior in SHANK2-mediated neuropsychiatric disordersAhmed Eltokhi, Miguel A Gonzalez-Lozano, Lars-Lennart Oettl, et al.
Hormone Research in Paediatrics|December 4, 2013
Alu-mediated recombination defect in IGF1R: haploinsufficiency in a patient with short statureEva-Maria Harmel, Gerhard Binder, Anja Barnikol-Oettler, et al.
Hormone Research in Paediatrics|May 20, 2020
Identification of Transient Receptor Potential Channel 4-Associated Protein as a Novel Candidate Gene Causing Congenital Primary HypothyroidismDaniela Choukair, Birgit Eberle, Philipp Vick, et al.
Pageof 8

Showing results (51-60 of 77) with videos related to

Sort By:
Pageof 8
Hormone Research in Paediatrics|May 14, 2015
Radiological Features in Patients with Short Stature Homeobox-Containing (SHOX) Gene Deficiency and Turner Syndrome before and after 2 Years of GH TreatmentChristopher J Child, Gabriel Kalifa, Christine Jones, et al.
Human Molecular Genetics|December 10, 2015
Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorderElliot Sollis, Sarah A Graham, Arianna Vino, et al.
Frontiers in Endocrinology|July 1, 2021
Evidence That Non-Syndromic Familial Tall Stature Has an Oligogenic Origin Including Ciliary GenesBirgit Weiss, Birgit Eberle, Ralph Roeth, et al.
The Journal of Biological Chemistry|May 18, 2004
The short stature homeodomain protein SHOX induces cellular growth arrest and apoptosis and is expressed in human growth plate chondrocytesAntonio Marchini, Tiina Marttila, Anja Winter, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2017
Identification of SLC20A1 and SLC15A4 among other genes as potential risk factors for combined pituitary hormone deficiencyFranziska Simm, Anne Griesbeck, Daniela Choukair, et al.
Molecular Psychiatry|May 22, 2021
Imbalanced post- and extrasynaptic SHANK2A functions during development affect social behavior in SHANK2-mediated neuropsychiatric disordersAhmed Eltokhi, Miguel A Gonzalez-Lozano, Lars-Lennart Oettl, et al.
Journal of the American Heart Association|January 22, 2026
<i>CAV1</i>-A Susceptibility Gene for Atrial Fibrillation: The Impact of Coding and Noncoding VariantsKristin Rädecke, David Rheinert, Annette Löwen, et al.
Molecular Psychiatry|July 8, 2021
Correction: Imbalanced post- and extrasynaptic SHANK2A functions during development affect social behavior in SHANK2-mediated neuropsychiatric disordersAhmed Eltokhi, Miguel A Gonzalez-Lozano, Lars-Lennart Oettl, et al.
Hormone Research in Paediatrics|December 4, 2013
Alu-mediated recombination defect in IGF1R: haploinsufficiency in a patient with short statureEva-Maria Harmel, Gerhard Binder, Anja Barnikol-Oettler, et al.
Hormone Research in Paediatrics|May 20, 2020
Identification of Transient Receptor Potential Channel 4-Associated Protein as a Novel Candidate Gene Causing Congenital Primary HypothyroidismDaniela Choukair, Birgit Eberle, Philipp Vick, et al.
Pageof 8