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Nature Communications
|
April 11, 2023
FOXI3 pathogenic variants cause one form of craniofacial microsomia
Ke Mao, Christelle Borel, Muhammad Ansar, et al.
Epilepsia
|
February 18, 2022
PIGN encephalopathy: Characterizing the epileptology
Allan Bayat, Guillem de Valles-Ibáñez, Manuela Pendziwiat, et al.
Human Genetics
|
May 24, 2024
The detection of a strong episignature for Chung-Jansen syndrome, partially overlapping with Börjeson-Forssman-Lehmann and White-Kernohan syndromes
Niels Vos, Sadegheh Haghshenas, Liselot van der Laan, et al.
HGG Advances
|
January 20, 2022
Novel diagnostic DNA methylation episignatures expand and refine the epigenetic landscapes of Mendelian disorders
Michael A Levy, Haley McConkey, Jennifer Kerkhof, et al.
American Journal of Human Genetics
|
July 16, 2024
Comprehensive EHMT1 variants analysis broadens genotype-phenotype associations and molecular mechanisms in Kleefstra syndrome
Dmitrijs Rots, Arianne Bouman, Ayumi Yamada, et al.
Human Mutation
|
July 29, 2022
Functional correlation of genome-wide DNA methylation profiles in genetic neurodevelopmental disorders
Michael A Levy, Raissa Relator, Haley McConkey, et al.
Nature
|
September 2, 2011
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus
Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey, et al.
Autophagy
|
January 23, 2016
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
Daniel J Klionsky, Kotb Abdelmohsen, Akihisa Abe, et al.
Autophagy
|
February 26, 2021
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)<sup>1</sup>
Daniel J Klionsky, Amal Kamal Abdel-Aziz, Sara Abdelfatah, et al.
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Search research articles
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Showing results (121-130 of 129) with videos related to
Sort By:
Page
of 13
You have reached the last page of results.
This site can display upto 129 results.
Nature Communications
|
April 11, 2023
FOXI3 pathogenic variants cause one form of craniofacial microsomia
Ke Mao, Christelle Borel, Muhammad Ansar, et al.
Epilepsia
|
February 18, 2022
PIGN encephalopathy: Characterizing the epileptology
Allan Bayat, Guillem de Valles-Ibáñez, Manuela Pendziwiat, et al.
Human Genetics
|
May 24, 2024
The detection of a strong episignature for Chung-Jansen syndrome, partially overlapping with Börjeson-Forssman-Lehmann and White-Kernohan syndromes
Niels Vos, Sadegheh Haghshenas, Liselot van der Laan, et al.
HGG Advances
|
January 20, 2022
Novel diagnostic DNA methylation episignatures expand and refine the epigenetic landscapes of Mendelian disorders
Michael A Levy, Haley McConkey, Jennifer Kerkhof, et al.
American Journal of Human Genetics
|
July 16, 2024
Comprehensive EHMT1 variants analysis broadens genotype-phenotype associations and molecular mechanisms in Kleefstra syndrome
Dmitrijs Rots, Arianne Bouman, Ayumi Yamada, et al.
Human Mutation
|
July 29, 2022
Functional correlation of genome-wide DNA methylation profiles in genetic neurodevelopmental disorders
Michael A Levy, Raissa Relator, Haley McConkey, et al.
Nature
|
September 2, 2011
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus
Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey, et al.
Autophagy
|
January 23, 2016
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
Daniel J Klionsky, Kotb Abdelmohsen, Akihisa Abe, et al.
Autophagy
|
February 26, 2021
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)<sup>1</sup>
Daniel J Klionsky, Amal Kamal Abdel-Aziz, Sara Abdelfatah, et al.
Page
of 13