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Journal of Medical Genetics
|
December 1, 2019
Linked-read genome sequencing identifies biallelic pathogenic variants in <i>DONSON</i> as a novel cause of Meier-Gorlin syndrome
Karen M Knapp, Rosie Sullivan, Jennie Murray, et al.
Molecular Cell
|
April 23, 2013
Ribonucleotides misincorporated into DNA act as strand-discrimination signals in eukaryotic mismatch repair
Medini Manohar Ghodgaonkar, Federico Lazzaro, Maite Olivera-Pimentel, et al.
Orphanet Journal of Rare Diseases
|
September 19, 2015
Meier-Gorlin syndrome
Sonja A de Munnik, Elisabeth H Hoefsloot, Jolt Roukema, et al.
Genome Research
|
July 15, 2018
Variant antigen repertoires in <i>Trypanosoma congolense</i> populations and experimental infections can be profiled from deep sequence data using universal protein motifs
Sara Silva Pereira, Aitor Casas-Sánchez, Lee R Haines, et al.
Nature
|
September 3, 2013
Cerebral organoids model human brain development and microcephaly
Madeline A Lancaster, Magdalena Renner, Carol-Anne Martin, et al.
Nature Communications
|
August 10, 2020
DONSON and FANCM associate with different replisomes distinguished by replication timing and chromatin domain
Jing Zhang, Marina A Bellani, Ryan C James, et al.
American Journal of Human Genetics
|
June 17, 2004
Mutations in microcephalin cause aberrant regulation of chromosome condensation
Marc Trimborn, Sandra M Bell, Clive Felix, et al.
Cancer Research
|
August 30, 2018
Ribonucleotide Excision Repair Is Essential to Prevent Squamous Cell Carcinoma of the Skin
Björn Hiller, Anja Hoppe, Christa Haase, et al.
Nature Genetics
|
December 25, 2007
Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signaling
Elen Griffith, Sarah Walker, Carol-Anne Martin, et al.
Nature
|
May 27, 2021
An invariant Trypanosoma vivax vaccine antigen induces protective immunity
Delphine Autheman, Cécile Crosnier, Simon Clare, et al.
Page
of 15
Search research articles
Search
Showing results (61-70 of 145) with videos related to
Sort By:
Page
of 15
Journal of Medical Genetics
|
December 1, 2019
Linked-read genome sequencing identifies biallelic pathogenic variants in <i>DONSON</i> as a novel cause of Meier-Gorlin syndrome
Karen M Knapp, Rosie Sullivan, Jennie Murray, et al.
Molecular Cell
|
April 23, 2013
Ribonucleotides misincorporated into DNA act as strand-discrimination signals in eukaryotic mismatch repair
Medini Manohar Ghodgaonkar, Federico Lazzaro, Maite Olivera-Pimentel, et al.
Orphanet Journal of Rare Diseases
|
September 19, 2015
Meier-Gorlin syndrome
Sonja A de Munnik, Elisabeth H Hoefsloot, Jolt Roukema, et al.
Genome Research
|
July 15, 2018
Variant antigen repertoires in <i>Trypanosoma congolense</i> populations and experimental infections can be profiled from deep sequence data using universal protein motifs
Sara Silva Pereira, Aitor Casas-Sánchez, Lee R Haines, et al.
Nature
|
September 3, 2013
Cerebral organoids model human brain development and microcephaly
Madeline A Lancaster, Magdalena Renner, Carol-Anne Martin, et al.
Nature Communications
|
August 10, 2020
DONSON and FANCM associate with different replisomes distinguished by replication timing and chromatin domain
Jing Zhang, Marina A Bellani, Ryan C James, et al.
American Journal of Human Genetics
|
June 17, 2004
Mutations in microcephalin cause aberrant regulation of chromosome condensation
Marc Trimborn, Sandra M Bell, Clive Felix, et al.
Cancer Research
|
August 30, 2018
Ribonucleotide Excision Repair Is Essential to Prevent Squamous Cell Carcinoma of the Skin
Björn Hiller, Anja Hoppe, Christa Haase, et al.
Nature Genetics
|
December 25, 2007
Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signaling
Elen Griffith, Sarah Walker, Carol-Anne Martin, et al.
Nature
|
May 27, 2021
An invariant Trypanosoma vivax vaccine antigen induces protective immunity
Delphine Autheman, Cécile Crosnier, Simon Clare, et al.
Page
of 15