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Christian Babbs

Showing results (21-30 of 47) with videos related to

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Methods and Protocols|June 6, 2019
Robust CRISPR/Cas9 Genome Editing of the HUDEP-2 Erythroid Precursor Line Using Plasmids and Single-Stranded Oligonucleotide DonorsGemma Moir-Meyer, Pak Leng Cheong, Aude-Anais Olijnik, et al.
British Journal of Haematology|April 13, 2022
Functional impairment of erythropoiesis in Congenital Dyserythropoietic Anaemia type I arises at the progenitor levelCaroline Scott, Kerol Bartolovic, Sally-Ann Clark, et al.
Journal of Medical Genetics|February 2, 2020
ATR-16 syndrome: mechanisms linking monosomy to phenotypeChristian Babbs, Jill Brown, Sharon W Horsley, et al.
Human Molecular Genetics|May 12, 2023
A new mouse model of ATR-X syndrome carrying a common patient mutation exhibits neurological and morphological defectsRebekah Tillotson, Keqin Yan, Julie Ruston, et al.
Haematologica|May 30, 2013
Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type IChristian Babbs, Nigel A Roberts, Luis Sanchez-Pulido, et al.
Nature Communications|July 2, 2026
CDIN1-Codanin-1 complex defective in congenital dyserythropoietic anaemia type I is an RNA nucleaseSanja Brolih, Hafiz Saqib Ali, Caroline Scott, et al.
Blood|January 21, 2014
Mutations in Kruppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expressionVip Viprakasit, Supachai Ekwattanakit, Suchada Riolueang, et al.
Nature Communications|September 23, 2018
A tissue-specific self-interacting chromatin domain forms independently of enhancer-promoter interactionsJill M Brown, Nigel A Roberts, Bryony Graham, et al.
Cell Death & Disease|May 28, 2026
MAFF regulates ferroptotic sensitivity through iron homeostasis and fatty acid synthesisNuria Vilaplana Lopera, Jiyoung Kim, Pei Ju Lee, et al.
Biorxiv : the Preprint Server for Biology|October 9, 2023
Ancient genomic linkage couples metabolism with erythroid developmentAlexandra E Preston, Joe N Frost, Mohsin Badat, et al.
Pageof 5

Showing results (21-30 of 47) with videos related to

Sort By:
Pageof 5
Methods and Protocols|June 6, 2019
Robust CRISPR/Cas9 Genome Editing of the HUDEP-2 Erythroid Precursor Line Using Plasmids and Single-Stranded Oligonucleotide DonorsGemma Moir-Meyer, Pak Leng Cheong, Aude-Anais Olijnik, et al.
British Journal of Haematology|April 13, 2022
Functional impairment of erythropoiesis in Congenital Dyserythropoietic Anaemia type I arises at the progenitor levelCaroline Scott, Kerol Bartolovic, Sally-Ann Clark, et al.
Journal of Medical Genetics|February 2, 2020
ATR-16 syndrome: mechanisms linking monosomy to phenotypeChristian Babbs, Jill Brown, Sharon W Horsley, et al.
Human Molecular Genetics|May 12, 2023
A new mouse model of ATR-X syndrome carrying a common patient mutation exhibits neurological and morphological defectsRebekah Tillotson, Keqin Yan, Julie Ruston, et al.
Haematologica|May 30, 2013
Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type IChristian Babbs, Nigel A Roberts, Luis Sanchez-Pulido, et al.
Nature Communications|July 2, 2026
CDIN1-Codanin-1 complex defective in congenital dyserythropoietic anaemia type I is an RNA nucleaseSanja Brolih, Hafiz Saqib Ali, Caroline Scott, et al.
Blood|January 21, 2014
Mutations in Kruppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expressionVip Viprakasit, Supachai Ekwattanakit, Suchada Riolueang, et al.
Nature Communications|September 23, 2018
A tissue-specific self-interacting chromatin domain forms independently of enhancer-promoter interactionsJill M Brown, Nigel A Roberts, Bryony Graham, et al.
Cell Death & Disease|May 28, 2026
MAFF regulates ferroptotic sensitivity through iron homeostasis and fatty acid synthesisNuria Vilaplana Lopera, Jiyoung Kim, Pei Ju Lee, et al.
Biorxiv : the Preprint Server for Biology|October 9, 2023
Ancient genomic linkage couples metabolism with erythroid developmentAlexandra E Preston, Joe N Frost, Mohsin Badat, et al.
Pageof 5