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European Journal of Medical Genetics
|
December 22, 2010
SNP-array based whole genome homozygosity mapping: a quick and powerful tool to achieve an accurate diagnosis in LGMD2 patients
Lea Papić, Dirk Fischer, Slave Trajanoski, et al.
European Journal of Endocrinology
|
May 14, 2025
Bariatric surgery promotes recruitment of brown fat linked to alterations in the gut microbiota
Carsten T Herz, Oana C Kulterer, Marlene Prager, et al.
Journal of Neurology
|
March 15, 2014
Whole-exome sequencing in patients with inherited neuropathies: outcome and challenges
Maria Schabhüttl, Thomas Wieland, Jan Senderek, et al.
Nutrients
|
March 26, 2022
Insights into the Composition of a Co-Culture of 10 Probiotic Strains (OMNi BiOTiC<sup>®</sup> AAD10) and Effects of Its Postbiotic Culture Supernatant
Bernhard Kienesberger, Beate Obermüller, Georg Singer, et al.
American Journal of Human Genetics
|
June 19, 2012
Exome sequencing identifies a REEP1 mutation involved in distal hereditary motor neuropathy type V
Christian Beetz, Thomas R Pieber, Nicole Hertel, et al.
The Journal of Investigative Dermatology
|
November 12, 2010
The dermoscopical and histopathological patterns of nevi correlate with the frequency of BRAF mutations
Iris Zalaudek, Christian Guelly, Giovanni Pellacani, et al.
The Journal of Investigative Dermatology
|
May 15, 2025
Urocanase-Positive Skin-Resident Bacteria Metabolize cis-Urocanic Acid and in Turn Reduce the Immunosuppressive Properties of UVR
VijayKumar Patra, Slave Trajanoski, Aaroh Joshi, et al.
Plos One
|
October 29, 2015
Lactobacillus casei Shirota Supplementation Does Not Restore Gut Microbiota Composition and Gut Barrier in Metabolic Syndrome: A Randomized Pilot Study
Vanessa Stadlbauer, Bettina Leber, Sandra Lemesch, et al.
Peerj
|
February 8, 2021
Patients with coronary heart disease, dilated cardiomyopathy and idiopathic ventricular tachycardia share overlapping patterns of pathogenic variation in cardiac risk genes
Christian Guelly, Zhannur Abilova, Omirbek Nuralinov, et al.
Journal of Neurology
|
September 6, 2011
SNP array-based whole genome homozygosity mapping as the first step to a molecular diagnosis in patients with Charcot-Marie-Tooth disease
Carina Fischer, Slave Trajanoski, Lea Papić, et al.
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of 6
Search research articles
Search
Showing results (41-50 of 53) with videos related to
Sort By:
Page
of 6
European Journal of Medical Genetics
|
December 22, 2010
SNP-array based whole genome homozygosity mapping: a quick and powerful tool to achieve an accurate diagnosis in LGMD2 patients
Lea Papić, Dirk Fischer, Slave Trajanoski, et al.
European Journal of Endocrinology
|
May 14, 2025
Bariatric surgery promotes recruitment of brown fat linked to alterations in the gut microbiota
Carsten T Herz, Oana C Kulterer, Marlene Prager, et al.
Journal of Neurology
|
March 15, 2014
Whole-exome sequencing in patients with inherited neuropathies: outcome and challenges
Maria Schabhüttl, Thomas Wieland, Jan Senderek, et al.
Nutrients
|
March 26, 2022
Insights into the Composition of a Co-Culture of 10 Probiotic Strains (OMNi BiOTiC<sup>®</sup> AAD10) and Effects of Its Postbiotic Culture Supernatant
Bernhard Kienesberger, Beate Obermüller, Georg Singer, et al.
American Journal of Human Genetics
|
June 19, 2012
Exome sequencing identifies a REEP1 mutation involved in distal hereditary motor neuropathy type V
Christian Beetz, Thomas R Pieber, Nicole Hertel, et al.
The Journal of Investigative Dermatology
|
November 12, 2010
The dermoscopical and histopathological patterns of nevi correlate with the frequency of BRAF mutations
Iris Zalaudek, Christian Guelly, Giovanni Pellacani, et al.
The Journal of Investigative Dermatology
|
May 15, 2025
Urocanase-Positive Skin-Resident Bacteria Metabolize cis-Urocanic Acid and in Turn Reduce the Immunosuppressive Properties of UVR
VijayKumar Patra, Slave Trajanoski, Aaroh Joshi, et al.
Plos One
|
October 29, 2015
Lactobacillus casei Shirota Supplementation Does Not Restore Gut Microbiota Composition and Gut Barrier in Metabolic Syndrome: A Randomized Pilot Study
Vanessa Stadlbauer, Bettina Leber, Sandra Lemesch, et al.
Peerj
|
February 8, 2021
Patients with coronary heart disease, dilated cardiomyopathy and idiopathic ventricular tachycardia share overlapping patterns of pathogenic variation in cardiac risk genes
Christian Guelly, Zhannur Abilova, Omirbek Nuralinov, et al.
Journal of Neurology
|
September 6, 2011
SNP array-based whole genome homozygosity mapping as the first step to a molecular diagnosis in patients with Charcot-Marie-Tooth disease
Carina Fischer, Slave Trajanoski, Lea Papić, et al.
Page
of 6