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Birth Defects Research
|
April 1, 2022
Re-sequencing of candidate genes FOXF1, HSPA6, HAAO, and KYNU in 522 individuals with VATER/VACTERL, VACTER/VACTERL-like association, and isolated anorectal malformation
Corina E Thiem, Jil D Stegmann, Alina C Hilger, et al.
Journal of Dental Research
|
September 16, 2021
MiRNA-149 as a Candidate for Facial Clefting and Neural Crest Cell Migration
L G Stüssel, R Hollstein, M Laugsch, et al.
American Journal of Human Genetics
|
April 18, 2025
A non-syndromic orofacial cleft risk locus links tRNA splicing defects to neural crest cell pathologies
Michaela Bartusel, Skylar X Kim, Rizwan Rehimi, et al.
Epigenomics
|
January 15, 2019
Evidence for DNA methylation mediating genetic liability to non-syndromic cleft lip/palate
Laurence J Howe, Tom G Richardson, Ryan Arathimos, et al.
Nature
|
February 19, 2026
Host control of persistent Epstein-Barr virus infection
Axel Schmidt, T Madhusankha Alawathurage, Friederike S David, et al.
European Journal of Oral Sciences
|
September 19, 2012
Evaluating SKI as a candidate gene for non-syndromic cleft lip with or without cleft palate
Elisabeth Mangold, Heiko Reutter, Rafael B R León-Cachón, et al.
Human Molecular Genetics
|
January 15, 2017
Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only
Kerstin U Ludwig, Anne C Böhmer, John Bowes, et al.
Clinical Epigenetics
|
January 16, 2024
Pancreatic cancer acquires resistance to MAPK pathway inhibition by clonal expansion and adaptive DNA hypermethylation
Laura K Godfrey, Jan Forster, Sven-Thorsten Liffers, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
June 22, 2010
Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population: Evidence for IRF6 and variants at 8q24 and 10q25
Augusto Rojas-Martinez, Heiko Reutter, Oscar Chacon-Camacho, et al.
Psychiatric Genetics
|
September 27, 2016
Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2
Franziska Degenhardt, Barbara Heinemann, Jana Strohmaier, et al.
Page
of 21
Search research articles
Search
Showing results (141-150 of 204) with videos related to
Sort By:
Page
of 21
Birth Defects Research
|
April 1, 2022
Re-sequencing of candidate genes FOXF1, HSPA6, HAAO, and KYNU in 522 individuals with VATER/VACTERL, VACTER/VACTERL-like association, and isolated anorectal malformation
Corina E Thiem, Jil D Stegmann, Alina C Hilger, et al.
Journal of Dental Research
|
September 16, 2021
MiRNA-149 as a Candidate for Facial Clefting and Neural Crest Cell Migration
L G Stüssel, R Hollstein, M Laugsch, et al.
American Journal of Human Genetics
|
April 18, 2025
A non-syndromic orofacial cleft risk locus links tRNA splicing defects to neural crest cell pathologies
Michaela Bartusel, Skylar X Kim, Rizwan Rehimi, et al.
Epigenomics
|
January 15, 2019
Evidence for DNA methylation mediating genetic liability to non-syndromic cleft lip/palate
Laurence J Howe, Tom G Richardson, Ryan Arathimos, et al.
Nature
|
February 19, 2026
Host control of persistent Epstein-Barr virus infection
Axel Schmidt, T Madhusankha Alawathurage, Friederike S David, et al.
European Journal of Oral Sciences
|
September 19, 2012
Evaluating SKI as a candidate gene for non-syndromic cleft lip with or without cleft palate
Elisabeth Mangold, Heiko Reutter, Rafael B R León-Cachón, et al.
Human Molecular Genetics
|
January 15, 2017
Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only
Kerstin U Ludwig, Anne C Böhmer, John Bowes, et al.
Clinical Epigenetics
|
January 16, 2024
Pancreatic cancer acquires resistance to MAPK pathway inhibition by clonal expansion and adaptive DNA hypermethylation
Laura K Godfrey, Jan Forster, Sven-Thorsten Liffers, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
June 22, 2010
Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population: Evidence for IRF6 and variants at 8q24 and 10q25
Augusto Rojas-Martinez, Heiko Reutter, Oscar Chacon-Camacho, et al.
Psychiatric Genetics
|
September 27, 2016
Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2
Franziska Degenhardt, Barbara Heinemann, Jana Strohmaier, et al.
Page
of 21