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ArticlesPeer ReviewedFull Text
Chromosome alignment‐maintaining phosphoprotein CHAMP1 plays a role in cell survival through regulating Mcl‐1 expression
Author / Creator:Hino, Maho ; Iemura, Kenji ; Ikeda, Masanori ; Itoh, Go ; Tanaka, Kozo
Publisher:Tokyo: John Wiley & Sons, Inc
Journal title:Cancer science, 2021-09, Vol.112 (9), p.3711-3721
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ArticlesPeer ReviewedFull Text
CHAMP1 complex directs heterochromatin assembly and promotes homology-directed DNA repair
Author / Creator:Li, Feng ; Zhang, Tianpeng ; Syed, Aleem ; Elbakry, Amira ; Holmer, Noella ; Nguyen, Huy ; Mukkavalli, Sirisha ; Greenberg, Roger A. ; D’Andrea, Alan D.
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2025-02, Vol.16 (1), p.1714-17
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ArticlesPeer ReviewedFull Text
CHAMP1 premature termination codon mutations found in individuals with intellectual disability cause a homologous recombination defect through haploinsufficiency
Author / Creator:Yoshizaki, Yujiro ; Ouchi, Yunosuke ; Kurniawan, Dicky ; Yumoto, Eisuke ; Yoneyama, Yuki ; Rizqullah, Faiza Ramadhani ; Sato, Hiyori ; Sarholz, Mirjam Hanako ; Natsume, Toyoaki ; Kanemaki, Masato T. ; Ikeda, Masanori ; Ui, Ayako ; Iemura, Kenji ; Tanaka, Kozo
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2024-12, Vol.14 (1), p.31904-15, Article 31904
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ArticlesPeer ReviewedFull Text
Prospective phenotyping of CHAMP1 disorder indicates that coding mutations may not act through haploinsufficiency
Author / Creator:Levy, Tess ; Pichardo, Thariana ; Silver, Hailey ; Lerman, Bonnie ; Zweifach, Jessica ; Halpern, Danielle ; Siper, Paige M. ; Kolevzon, Alexander ; Buxbaum, Joseph D.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Human genetics, 2023-09, Vol.142 (9), p.1385-1394
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ArticlesFull Text
First Chinese patient with mental retardation‑40 due to a de novo CHAMP1 frameshift mutation: Case report and literature review
Author / Creator:Dong, Yan ; Shi, Xiaoyi ; Du, Kaixian ; Xu, Ruijuan ; Jia, Tianming ; Wang, Jun ; Wang, Lijun ; Han, Rui
Publisher:Athens: Spandidos Publications UK Ltd
Journal title:Experimental and therapeutic medicine, 2021-08, Vol.22 (2), Article 907
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ArticlesPeer ReviewedFull Text
Chromodomain on Y-like 2 (CDYL2) implicated in mitosis and genome stability regulation via interaction with CHAMP1 and POGZ
Author / Creator:Siouda, Maha ; Dujardin, Audrey D. ; Dekeyzer, Blanche ; Schaeffer, Laurent ; Mulligan, Peter
Publisher:Cham: Springer International Publishing
Journal title:Cellular and molecular life sciences : CMLS, 2023-02, Vol.80 (2), p.47-47, Article 47
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ArticlesPeer ReviewedFull Text
Intellectual disability and microcephaly associated with a novel CHAMP1 mutation
Author / Creator:Asakura, Yuta ; Osaka, Hitoshi ; Aoi, Hiromi ; Mizuguchi, Takeshi ; Matsumoto, Naomichi ; Yamagata, Takanori
Publisher:London: Nature Publishing Group UK
Journal title:Human genome variation, 2021-08, Vol.8 (1), p.34-34, Article 34
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ArticlesPeer ReviewedFull Text
Disturbed chromosome segregation and multipolar spindle formation in a patient with CHAMP1 mutation
Author / Creator:Okamoto, Nobuhiko ; Tsuchiya, Yuki ; Kuki, Ichiro ; Yamamoto, Toshiyuki ; Saitsu, Hirotomo ; Kitagawa, Daiju ; Matsumoto, Naomichi
Publisher:United States: John Wiley and Sons Inc
Journal title:Molecular genetics & genomic medicine, 2017-09, Vol.5 (5), p.585-591
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ArticlesFull Text
CHAMP1 complex directs heterochromatin assembly and promotes homology-directed DNA repair (Updated September 25, 2024)
Publisher:NewsRX LLC
Journal title:Obesity, fitness, & wellness week, 2024-10, p.797
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ArticlesPeer ReviewedFull Text
CHAMP1-Related Disorder: Sharing 20 Years of thorough Clinical Follow-Up and Review of the Literature
Author / Creator:Abi Raad, Sarah ; Yazbeck Karam, Vanda ; Chouery, Eliane ; Mehawej, Cybel ; Megarbane, Andre
Publisher:Basel: MDPI AG
Journal title:Genes, 2023-07, Vol.14 (8), p.1546
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ArticlesFull Text
Harvard Medical School Researchers Describe New Findings in Chromatin (CHAMP1 complex directs heterochromatin assembly and promotes homology-directed DNA repair)
Publisher:NewsRX LLC
Journal title:Obesity, fitness, & wellness week, 2025-03, p.1946
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ArticlesFull Text
REV7/FANCV Binds to CHAMP1 and Promotes Homologous Recombination Repair
Author / Creator:Li, Feng ; Sarangi, Prabha ; Feng, Hanrong ; Moreau, Lisa ; Nguyen, Huy ; Connor Clairmont ; D'andrea, Alan D
Publisher:Cold Spring Harbor: Cold Spring Harbor Laboratory Press
Journal title:bioRxiv, 2021-10
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ArticlesFull Text
LA NOTION ÉLARGIE DE CHAMP1
Author / Creator:Neri, Claudio
Publisher:Geneva: Éditions Médecine et Hygiène
Journal title:Psychothérapies (Geneva, Switzerland), 2007-01, Vol.27 (1), p.19
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ArticlesFull Text
Findings from Icahn School of Medicine at Mount Sinai Provides New Data about Life Science (Prospective Phenotyping of Champ1 Disorder Indicates That Coding Mutations May Not Act Through Haploinsuffic...
Publisher:NewsRX LLC
Journal title:Obesity, fitness, & wellness week, 2023-08, p.1296
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Newsletter articlesFull Text
REV7/FANCV Binds to CHAMP1 and Promotes Homologous Recombination Repair
Publisher:NewsRX LLC
Journal title:Life Science Weekly, 2021, p.3478
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Newsletter articlesFull Text
First study to directly compare gene mutation type in individuals with CHAMP1 disorder indicates key differences
Publisher:NewsRX LLC
Journal title:Mental Health Weekly Digest, 2023, p.336
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Newsletter articlesFull Text
Prospective phenotyping of CHAMP1 disorder indicates that coding mutations do not act through haploinsufficiency
Publisher:NewsRX LLC
Journal title:Health & Medicine Week, 2023, p.3497
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ArticlesFull Text
Studies from Zhengzhou University in the Area of Intellectual Disability Described (First Chinese Patient With Mental Retardation-40 Due To a De Novo Champ1 Frameshift Mutation: Case Report and Litera...
Publisher:NewsRX LLC
Journal title:Obesity, fitness, & wellness week, 2021-08, p.714
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Newsletter articlesFull Text
Researchers reveal the role of the CHAMP1 gene in neuronal development
Publisher:NewsRX LLC
Journal title:NewsRx Health, 2022, p.329-329
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Newsletter articlesFull Text
The Mount Sinai Hospital First Study to Directly Compare Gene Mutation Type in Individuals With CHAMP1 Disorder Indicates Key Differences
Publisher:Melbourne: News Bites Pty Ltd
Journal title:News Bites - Private Companies, 2023
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Chromosome alignment‐maintaining phosphoprotein CHAMP1 plays a role in cell survival through regulating Mcl‐1 expression

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CHAMP1 complex directs heterochromatin assembly and promotes homology-directed DNA repair

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CHAMP1 premature termination codon mutations found in individuals with intellectual disability cause a homologous recombination defect through haploinsufficiency

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Prospective phenotyping of CHAMP1 disorder indicates that coding mutations may not act through haploinsufficiency

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First Chinese patient with mental retardation‑40 due to a de novo CHAMP1 frameshift mutation: Case report and literature review

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Chromodomain on Y-like 2 (CDYL2) implicated in mitosis and genome stability regulation via interaction with CHAMP1 and POGZ

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Intellectual disability and microcephaly associated with a novel CHAMP1 mutation

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Disturbed chromosome segregation and multipolar spindle formation in a patient with CHAMP1 mutation

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CHAMP1 complex directs heterochromatin assembly and promotes homology-directed DNA repair (Updated September 25, 2024)

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CHAMP1-Related Disorder: Sharing 20 Years of thorough Clinical Follow-Up and Review of the Literature

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Harvard Medical School Researchers Describe New Findings in Chromatin (CHAMP1 complex directs heterochromatin assembly and promotes homology-directed DNA repair)

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REV7/FANCV Binds to CHAMP1 and Promotes Homologous Recombination Repair

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LA NOTION ÉLARGIE DE CHAMP1

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Findings from Icahn School of Medicine at Mount Sinai Provides New Data about Life Science (Prospective Phenotyping of Champ1 Disorder Indicates That Coding Mutations May Not Act Through Haploinsuffic...

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REV7/FANCV Binds to CHAMP1 and Promotes Homologous Recombination Repair

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First study to directly compare gene mutation type in individuals with CHAMP1 disorder indicates key differences

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Prospective phenotyping of CHAMP1 disorder indicates that coding mutations do not act through haploinsufficiency

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Studies from Zhengzhou University in the Area of Intellectual Disability Described (First Chinese Patient With Mental Retardation-40 Due To a De Novo Champ1 Frameshift Mutation: Case Report and Litera...

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Researchers reveal the role of the CHAMP1 gene in neuronal development

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The Mount Sinai Hospital First Study to Directly Compare Gene Mutation Type in Individuals With CHAMP1 Disorder Indicates Key Differences

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