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European Journal of Human Genetics : EJHG
|
March 17, 2005
Novel mutations in BCOR in three patients with oculo-facio-cardio-dental syndrome, but none in Lenz microphthalmia syndrome
Denise Horn, Magdalena Chyrek, Saskia Kleier, et al.
Journal of Molecular and Cellular Cardiology
|
February 23, 2017
Disrupting the key circadian regulator CLOCK leads to age-dependent cardiovascular disease
Faisal J Alibhai, Jonathan LaMarre, Cristine J Reitz, et al.
Journal of Human Genetics
|
April 27, 2023
Expanding the phenotypic spectrum and clinical severity associated with WLS gene
Ghada M H Abdel-Salam, Hanan H Afifi, Mohamed S Abdel-Hamid, et al.
Plos One
|
March 9, 2010
Helicobacter pylori induces miR-155 in T cells in a cAMP-Foxp3-dependent manner
Lina Fassi Fehri, Manuel Koch, Elena Belogolova, et al.
Kidney International
|
June 21, 2021
NPHP1 gene-associated nephronophthisis is associated with an occult retinopathy
Johannes Birtel, Georg Spital, Marius Book, et al.
Pharmaceutics
|
January 21, 2022
Pharmacokinetics of Pullulan-Dexamethasone Conjugates in Retinal Drug Delivery
Eva Kicková, Amir Sadeghi, Jooseppi Puranen, et al.
Plos Neglected Tropical Diseases
|
June 21, 2013
Geographic distribution, age pattern and sites of lesions in a cohort of Buruli ulcer patients from the Mapé Basin of Cameroon
Martin W Bratschi, Miriam Bolz, Jacques C Minyem, et al.
Scientific Reports
|
March 21, 2018
Clinical and genetic characteristics of 251 consecutive patients with macular and cone/cone-rod dystrophy
Johannes Birtel, Tobias Eisenberger, Martin Gliem, et al.
Cardiovascular Research
|
November 23, 2022
Disrupting circadian control of peripheral myogenic reactivity mitigates cardiac injury following myocardial infarction
Jeffrey T Kroetsch, Darcy Lidington, Faisal J Alibhai, et al.
Plos One
|
February 4, 2015
An efficient and comprehensive strategy for genetic diagnostics of polycystic kidney disease
Tobias Eisenberger, Christian Decker, Milan Hiersche, et al.
Page
of 87
Search research articles
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Showing results (691-700 of 866) with videos related to
Sort By:
Page
of 87
European Journal of Human Genetics : EJHG
|
March 17, 2005
Novel mutations in BCOR in three patients with oculo-facio-cardio-dental syndrome, but none in Lenz microphthalmia syndrome
Denise Horn, Magdalena Chyrek, Saskia Kleier, et al.
Journal of Molecular and Cellular Cardiology
|
February 23, 2017
Disrupting the key circadian regulator CLOCK leads to age-dependent cardiovascular disease
Faisal J Alibhai, Jonathan LaMarre, Cristine J Reitz, et al.
Journal of Human Genetics
|
April 27, 2023
Expanding the phenotypic spectrum and clinical severity associated with WLS gene
Ghada M H Abdel-Salam, Hanan H Afifi, Mohamed S Abdel-Hamid, et al.
Plos One
|
March 9, 2010
Helicobacter pylori induces miR-155 in T cells in a cAMP-Foxp3-dependent manner
Lina Fassi Fehri, Manuel Koch, Elena Belogolova, et al.
Kidney International
|
June 21, 2021
NPHP1 gene-associated nephronophthisis is associated with an occult retinopathy
Johannes Birtel, Georg Spital, Marius Book, et al.
Pharmaceutics
|
January 21, 2022
Pharmacokinetics of Pullulan-Dexamethasone Conjugates in Retinal Drug Delivery
Eva Kicková, Amir Sadeghi, Jooseppi Puranen, et al.
Plos Neglected Tropical Diseases
|
June 21, 2013
Geographic distribution, age pattern and sites of lesions in a cohort of Buruli ulcer patients from the Mapé Basin of Cameroon
Martin W Bratschi, Miriam Bolz, Jacques C Minyem, et al.
Scientific Reports
|
March 21, 2018
Clinical and genetic characteristics of 251 consecutive patients with macular and cone/cone-rod dystrophy
Johannes Birtel, Tobias Eisenberger, Martin Gliem, et al.
Cardiovascular Research
|
November 23, 2022
Disrupting circadian control of peripheral myogenic reactivity mitigates cardiac injury following myocardial infarction
Jeffrey T Kroetsch, Darcy Lidington, Faisal J Alibhai, et al.
Plos One
|
February 4, 2015
An efficient and comprehensive strategy for genetic diagnostics of polycystic kidney disease
Tobias Eisenberger, Christian Decker, Milan Hiersche, et al.
Page
of 87