Search research articles
Contact Us
Filters
Showing results (101-110 of 338) with videos related to
Page
of 34
Sort By:
European Journal of Human Genetics : EJHG
|
June 19, 2014
Germline PTPN11 and somatic PIK3CA variant in a boy with megalencephaly-capillary malformation syndrome (MCAP)--pure coincidence?
Dennis Döcker, Max Schubach, Moritz Menzel, et al.
Thrombosis Research
|
April 3, 2002
Differences between neonates and adults in carbohydrate sequences and reaction kinetics of plasmin and alpha(2)-antiplasmin
Martin Ries, Richard L Easton, Colin Longstaff, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
June 15, 2013
Impaired motor cortex plasticity in patients with Noonan syndrome
Florian Mainberger, Martin Zenker, Nikolai H Jung, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
September 17, 2024
Cancer in Multilineage Mosaic RASopathies due to Pathogenic Variants in HRAS or KRAS: A Systematic Review and Meta-analysis
Jonas Windrich, Gina M Ney, Philip S Rosenberg, et al.
Molecular Nutrition & Food Research
|
November 1, 2018
Food-Derived Xeno-microRNAs: Influence of Diet and Detectability in Gastrointestinal Tract-Proof-of-Principle Study
Jastin Link, Cosima Thon, Denny Schanze, et al.
Human Molecular Genetics
|
October 13, 2012
Diverging gain-of-function mechanisms of two novel KRAS mutations associated with Noonan and cardio-facio-cutaneous syndromes
Ion C Cirstea, Lothar Gremer, Radovan Dvorsky, et al.
Molecular Psychiatry
|
June 11, 2024
Differential methylation of OPRK1 in borderline personality disorder is associated with childhood trauma
Dorothee Maria Gescher, Denny Schanze, Peter Vavra, et al.
Endocrine Connections
|
March 4, 2022
Outcomes in growth hormone-treated Noonan syndrome children: impact of PTPN11 mutation status
Alexander A L Jorge, Thomas Edouard, Mohamad Maghnie, et al.
Pigment Cell & Melanoma Research
|
December 15, 2018
Detection of a multilineage mosaic NRAS mutation c.181C>A (p.Gln61Lys) in an individual with a complex congenital nevus syndrome
Maximilian Ulrich, Sigrid Tinschert, Eberhard Siebert, et al.
Journal of the Neurological Sciences
|
October 19, 2015
Hereditary diffuse leukoencephalopathy with spheroids (HDLS) with a novel CSF1R mutation and spinal cord involvement
Peter Körtvelyessy, Ingeborg Krägeloh-Mann, Christian Mawrin, et al.
Page
of 34
Search research articles
Search
Showing results (101-110 of 338) with videos related to
Sort By:
Page
of 34
European Journal of Human Genetics : EJHG
|
June 19, 2014
Germline PTPN11 and somatic PIK3CA variant in a boy with megalencephaly-capillary malformation syndrome (MCAP)--pure coincidence?
Dennis Döcker, Max Schubach, Moritz Menzel, et al.
Thrombosis Research
|
April 3, 2002
Differences between neonates and adults in carbohydrate sequences and reaction kinetics of plasmin and alpha(2)-antiplasmin
Martin Ries, Richard L Easton, Colin Longstaff, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
June 15, 2013
Impaired motor cortex plasticity in patients with Noonan syndrome
Florian Mainberger, Martin Zenker, Nikolai H Jung, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
September 17, 2024
Cancer in Multilineage Mosaic RASopathies due to Pathogenic Variants in HRAS or KRAS: A Systematic Review and Meta-analysis
Jonas Windrich, Gina M Ney, Philip S Rosenberg, et al.
Molecular Nutrition & Food Research
|
November 1, 2018
Food-Derived Xeno-microRNAs: Influence of Diet and Detectability in Gastrointestinal Tract-Proof-of-Principle Study
Jastin Link, Cosima Thon, Denny Schanze, et al.
Human Molecular Genetics
|
October 13, 2012
Diverging gain-of-function mechanisms of two novel KRAS mutations associated with Noonan and cardio-facio-cutaneous syndromes
Ion C Cirstea, Lothar Gremer, Radovan Dvorsky, et al.
Molecular Psychiatry
|
June 11, 2024
Differential methylation of OPRK1 in borderline personality disorder is associated with childhood trauma
Dorothee Maria Gescher, Denny Schanze, Peter Vavra, et al.
Endocrine Connections
|
March 4, 2022
Outcomes in growth hormone-treated Noonan syndrome children: impact of PTPN11 mutation status
Alexander A L Jorge, Thomas Edouard, Mohamad Maghnie, et al.
Pigment Cell & Melanoma Research
|
December 15, 2018
Detection of a multilineage mosaic NRAS mutation c.181C>A (p.Gln61Lys) in an individual with a complex congenital nevus syndrome
Maximilian Ulrich, Sigrid Tinschert, Eberhard Siebert, et al.
Journal of the Neurological Sciences
|
October 19, 2015
Hereditary diffuse leukoencephalopathy with spheroids (HDLS) with a novel CSF1R mutation and spinal cord involvement
Peter Körtvelyessy, Ingeborg Krägeloh-Mann, Christian Mawrin, et al.
Page
of 34