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Basic Research in Cardiology
|
May 4, 2016
Coding and non-coding variants in the SHOX2 gene in patients with early-onset atrial fibrillation
Sandra Hoffmann, Sebastian Clauss, Ina M Berger, et al.
Molecular Neurodegeneration
|
June 3, 2021
Parkinson mice show functional and molecular changes in the gut long before motoric disease onset
Manuela Gries, Anne Christmann, Steven Schulte, et al.
Human Mutation
|
September 18, 2010
Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits
Denise Horn, Johannes Kapeller, Núria Rivera-Brugués, et al.
American Journal of Human Genetics
|
April 17, 2012
SHANK1 Deletions in Males with Autism Spectrum Disorder
Daisuke Sato, Anath C Lionel, Claire S Leblond, et al.
Cell Death & Disease
|
May 30, 2024
Biallelic variants in CSMD1 are implicated in a neurodevelopmental disorder with intellectual disability and variable cortical malformations
Elizabeth A Werren, Emily R Peirent, Henna Jantti, et al.
Plos Genetics
|
November 5, 2020
A complementary study approach unravels novel players in the pathoetiology of Hirschsprung disease
Tanja Mederer, Stefanie Schmitteckert, Julia Volz, et al.
Scientific Reports
|
November 2, 2017
miR-16 and miR-103 impact 5-HT<sub>4</sub> receptor signalling and correlate with symptom profile in irritable bowel syndrome
Carolin Wohlfarth, Stefanie Schmitteckert, Janina D Härtle, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
September 19, 2022
The serotonin receptor 3E variant is a risk factor for female IBS-D
Nikola Fritz, Sabrina Berens, Yuanjun Dong, et al.
Journal of Cellular and Molecular Medicine
|
June 24, 2021
The alternative serotonin transporter promoter P2 impacts gene function in females with irritable bowel syndrome
Sandra Mohr, Nikola Fritz, Christian Hammer, et al.
Plos Genetics
|
September 5, 2014
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments
Claire S Leblond, Caroline Nava, Anne Polge, et al.
Page
of 16
Search research articles
Search
Showing results (151-160 of 160) with videos related to
Sort By:
Page
of 16
You have reached the last page of results.
This site can display upto 160 results.
Basic Research in Cardiology
|
May 4, 2016
Coding and non-coding variants in the SHOX2 gene in patients with early-onset atrial fibrillation
Sandra Hoffmann, Sebastian Clauss, Ina M Berger, et al.
Molecular Neurodegeneration
|
June 3, 2021
Parkinson mice show functional and molecular changes in the gut long before motoric disease onset
Manuela Gries, Anne Christmann, Steven Schulte, et al.
Human Mutation
|
September 18, 2010
Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits
Denise Horn, Johannes Kapeller, Núria Rivera-Brugués, et al.
American Journal of Human Genetics
|
April 17, 2012
SHANK1 Deletions in Males with Autism Spectrum Disorder
Daisuke Sato, Anath C Lionel, Claire S Leblond, et al.
Cell Death & Disease
|
May 30, 2024
Biallelic variants in CSMD1 are implicated in a neurodevelopmental disorder with intellectual disability and variable cortical malformations
Elizabeth A Werren, Emily R Peirent, Henna Jantti, et al.
Plos Genetics
|
November 5, 2020
A complementary study approach unravels novel players in the pathoetiology of Hirschsprung disease
Tanja Mederer, Stefanie Schmitteckert, Julia Volz, et al.
Scientific Reports
|
November 2, 2017
miR-16 and miR-103 impact 5-HT<sub>4</sub> receptor signalling and correlate with symptom profile in irritable bowel syndrome
Carolin Wohlfarth, Stefanie Schmitteckert, Janina D Härtle, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
September 19, 2022
The serotonin receptor 3E variant is a risk factor for female IBS-D
Nikola Fritz, Sabrina Berens, Yuanjun Dong, et al.
Journal of Cellular and Molecular Medicine
|
June 24, 2021
The alternative serotonin transporter promoter P2 impacts gene function in females with irritable bowel syndrome
Sandra Mohr, Nikola Fritz, Christian Hammer, et al.
Plos Genetics
|
September 5, 2014
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments
Claire S Leblond, Caroline Nava, Anne Polge, et al.
Page
of 16