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W Brouwer

Showing results (201-210 of 227) with videos related to

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Biological Psychiatry|October 18, 2016
Nonsynonymous Variation in NKPD1 Increases Depressive Symptoms in European PopulationsNajaf Amin, Nadezhda M Belonogova, Olivera Jovanova, et al.
Cell Reports|May 21, 2020
MAU2 and NIPBL Variants Impair the Heterodimerization of the Cohesin Loader Subunits and Cause Cornelia de Lange SyndromeIlaria Parenti, Farah Diab, Sara Ruiz Gil, et al.
American Journal of Human Genetics|June 13, 2017
Loss-of-Function Variants in MYLK Cause Recessive Megacystis Microcolon Intestinal Hypoperistalsis SyndromeDanny Halim, Erwin Brosens, Françoise Muller, et al.
Gastroenterology|March 31, 2018
Identification of Variants in RET and IHH Pathway Members in a Large Family With History of Hirschsprung DiseaseYunia Sribudiani, Rajendra K Chauhan, Maria M Alves, et al.
Birth Defects Research|April 17, 2020
Infantile hypertrophic pyloric stenosis in patients with esophageal atresiaChantal A Ten Kate, Rutger W W Brouwer, Yolande van Bever, et al.
Nature Cell Biology|May 6, 2020
In vitro capture and characterization of embryonic rosette-stage pluripotency between naive and primed statesAlex Neagu, Emiel van Genderen, Irene Escudero, et al.
Journal of Leukocyte Biology|December 8, 2020
Comparison of the PU.1 transcriptional regulome and interactome in human and mouse inflammatory dendritic cellsMaaike R Scheenstra, Patricia Martínez-Botía, Andrea Acebes-Huerta, et al.
Blood Advances|May 3, 2021
Molecular analysis of the erythroid phenotype of a patient with BCL11A haploinsufficiencyMarja W Wessels, Marjon H Cnossen, Thamar B van Dijk, et al.
Leukemia|November 6, 2021
The tumor suppressor MIR139 is silenced by POLR2M to promote AML oncogenesisChristiaan J Stavast, Iris van Zuijen, Elena Karkoulia, et al.
Molecular Psychiatry|March 22, 2017
A rare missense variant in RCL1 segregates with depression in extended familiesN Amin, F M S de Vrij, M Baghdadi, et al.
Pageof 23

Showing results (201-210 of 227) with videos related to

Sort By:
Pageof 23
Biological Psychiatry|October 18, 2016
Nonsynonymous Variation in NKPD1 Increases Depressive Symptoms in European PopulationsNajaf Amin, Nadezhda M Belonogova, Olivera Jovanova, et al.
Cell Reports|May 21, 2020
MAU2 and NIPBL Variants Impair the Heterodimerization of the Cohesin Loader Subunits and Cause Cornelia de Lange SyndromeIlaria Parenti, Farah Diab, Sara Ruiz Gil, et al.
American Journal of Human Genetics|June 13, 2017
Loss-of-Function Variants in MYLK Cause Recessive Megacystis Microcolon Intestinal Hypoperistalsis SyndromeDanny Halim, Erwin Brosens, Françoise Muller, et al.
Gastroenterology|March 31, 2018
Identification of Variants in RET and IHH Pathway Members in a Large Family With History of Hirschsprung DiseaseYunia Sribudiani, Rajendra K Chauhan, Maria M Alves, et al.
Birth Defects Research|April 17, 2020
Infantile hypertrophic pyloric stenosis in patients with esophageal atresiaChantal A Ten Kate, Rutger W W Brouwer, Yolande van Bever, et al.
Nature Cell Biology|May 6, 2020
In vitro capture and characterization of embryonic rosette-stage pluripotency between naive and primed statesAlex Neagu, Emiel van Genderen, Irene Escudero, et al.
Journal of Leukocyte Biology|December 8, 2020
Comparison of the PU.1 transcriptional regulome and interactome in human and mouse inflammatory dendritic cellsMaaike R Scheenstra, Patricia Martínez-Botía, Andrea Acebes-Huerta, et al.
Blood Advances|May 3, 2021
Molecular analysis of the erythroid phenotype of a patient with BCL11A haploinsufficiencyMarja W Wessels, Marjon H Cnossen, Thamar B van Dijk, et al.
Leukemia|November 6, 2021
The tumor suppressor MIR139 is silenced by POLR2M to promote AML oncogenesisChristiaan J Stavast, Iris van Zuijen, Elena Karkoulia, et al.
Molecular Psychiatry|March 22, 2017
A rare missense variant in RCL1 segregates with depression in extended familiesN Amin, F M S de Vrij, M Baghdadi, et al.
Pageof 23