K. Usdin

发表

Use of model systems to understand the etiology of fragile X-associated primary ovarian insufficiency (FXPOI)

P. Jin, M. Tejada, R. Willemsen, 2014, Journal of Neurodevelopmental Disorders.

CHAPTER 39 – Bending the Rules: Unusual Nucleic Acid Structures and Disease Pathology in the Repeat Expansion Diseases

K. Usdin, 2006 .

The biological effects of simple tandem repeats: lessons from the repeat expansion diseases.

Karen Usdin, K. Usdin, 2008, Genome research.

The Mismatch Repair Protein MSH2 is Rate Limiting for Repeat Expansion in a Fragile X Premutation Mouse Model

K. Usdin, R. Lokanga, Xiaonan Zhao, 2014, Human mutation.

The Development and Use of a DNA Polymerase Arrest Assay for the Evaluation of Parameters Affecting Intrastrand Tetraplex Formation*

K. Woodford, K. Usdin, M. Weitzmann, 1996, The Journal of Biological Chemistry.

Human nucleotide expansion disorders

M. Fry, K. Usdin, 2006 .

Improved Assays for AGG Interruptions in Fragile X Premutation Carriers.

B. Hayward, K. Usdin, 2017, The Journal of molecular diagnostics : JMD.

Stool is a sensitive and noninvasive source of DNA for monitoring expansion in repeat expansion disease mouse models

J. Carroll, K. Usdin, Xiaonan Zhao, 2022, Disease models & mechanisms.

MutLγ promotes repeat expansion in a Fragile X mouse model while EXO1 is protective

W. Edelmann, K. Usdin, Yongwei Zhang, 2018, PLoS genetics.

A MutSβ-Dependent Contribution of MutSα to Repeat Expansions in Fragile X Premutation Mice?

K. Allette, K. Usdin, R. Lokanga, 2016, PLoS genetics.

The Transcription‐Coupled Repair Protein ERCC6/CSB Also Protects Against Repeat Expansion in a Mouse Model of the Fragile X Premutation

K. Usdin, Xiaonan Zhao, 2015, Human mutation.

Heterozygosity for a Hypomorphic Polβ Mutation Reduces the Expansion Frequency in a Mouse Model of the Fragile X-Related Disorders

J. Sweasy, K. Usdin, R. Lokanga, 2015, PLoS genetics.

X inactivation plays a major role in the gender bias in somatic expansion in a mouse model of the fragile X-related disorders: implications for the mechanism of repeat expansion.

K. Usdin, Xiaonan Zhao, A. Entezam, 2014, Human molecular genetics.

Somatic Expansion in Mouse and Human Carriers of Fragile X Premutation Alleles

C. B. Smith, K. Usdin, R. Lokanga, 2013, Human mutation.

Repeat expansions confer WRN dependence in microsatellite-unstable cancers

K. Garimella, S. West, P. Meltzer, 2020, Nature.

Molecular analysis of FMR1 alleles for fragile X syndrome diagnosis and patient stratification

K. Usdin, D. Kumari, 2020, Expert review of molecular diagnostics.

CGG Repeat Expansion, and Elevated Fmr1 Transcription and Mitochondrial Copy Number in a New Fragile X PM Mouse Embryonic Stem Cell Model

Carson J Miller, K. Usdin, I. Gazy, 2020, Frontiers in Cell and Developmental Biology.

Rat L (long interspersed repeated DNA) elements contain guanine-rich homopurine sequences that induce unpairing of contiguous duplex DNA.

A. Furano, K. Usdin, 1988, Proceedings of the National Academy of Sciences of the United States of America.

CGG-repeat dynamics and FMR1 gene silencing in fragile X syndrome stem cells and stem cell-derived neurons

Yifan Zhou, K. Usdin, D. Kumari, 2016, Molecular Autism.

Evidence for the wide distribution of repetitive DNA sequences in the genusStreptomyces

R. Kirby, K. Usdin, K. Gertsch, 2005, Journal of Molecular Evolution.

S1-END-seq reveals DNA secondary structures in human cells.

S. Mirkin, A. Nussenzweig, A. Ansari, 2022, Molecular cell.

Identification of Fragile X Syndrome Specific Molecular Markers in Human Fibroblasts: A Useful Model to Test the Efficacy of Therapeutic Drugs

E. Klann, C. B. Smith, Kristen Moulton, 2014, Human mutation.

Tetraplex formation by the progressive myoclonus epilepsy type‐1 repeat: implications for instability in the repeat expansion diseases

K. Usdin, Tapas Saha, 2001, FEBS letters.

FAN1 protects against repeat expansions in a Fragile X mouse model.

K. Usdin, Xiaonan Zhao, 2018, DNA repair.

Recent advances in assays for the fragile X-related disorders

B. Hayward, K. Usdin, D. Kumari, 2017, Human Genetics.

Instability of the fragile X syndrome repeat in mice: the effect of age, diet and mutations in genes that affect DNA replication, recombination and repair proficiency

K. Usdin, D. Kumari, D. Riser, 2003, Cytogenetic and Genome Research.

Assays for Determining Repeat Number, Methylation Status, and AGG Interruptions in the Fragile X-Related Disorders.

B. Hayward, K. Usdin, 2019, Methods in molecular biology.

Glutaminase Deficiency Caused by Short Tandem Repeat Expansion in GLS

Phillip A. Richmond, S. Scherer, R. Yuen, 2019, The New England journal of medicine.

Both cis and trans-acting genetic factors drive somatic instability in female carriers of the FMR1 premutation

P. Holmans, F. Tassone, B. Hayward, 2022, Scientific Reports.

Granulosa cell and oocyte mitochondrial abnormalities in a mouse model of fragile X primary ovarian insufficiency.

C. Giulivi, M. Ferrari, S. Bellone, 2016, Molecular human reproduction.

Fragile X syndrome in a male with methylated premutation alleles and no detectable methylated full mutation alleles

C. B. Smith, A. Thurm, Inna Loutaev, 2019, American journal of medical genetics. Part A.

Cloning of repeated DNA sequences from Streptomyces cattleya

R. Kirby, K. Usdin, 1988 .

Repeat Expansions Confers WRN Dependence in Microsatellite Unstable 1 Cancers

Anthony, Tubbs, K. Garimella, 2020 .

A novel K(+)-dependent DNA synthesis arrest site in a commonly occurring sequence motif in eukaryotes.

K. Woodford, K. Usdin, R. Howell, 1994, The Journal of biological chemistry.

Cloning, Expression, and Purification of Glutamine Synthetase from Clostridium acetobutylicum

David T. Jones, D. R. Woods, H. Zappe, 1986, Applied and environmental microbiology.

NGG-triplet repeats form similar intrastrand structures: implications for the triplet expansion diseases.

K. Usdin, 1998, Nucleic acids research.

The Chicken -Globin Gene Promoter Forms a Novel Cinched Tetrahelical Structure (*)

K. Usdin, K. Woodford, K. Usdin, 1996, The Journal of Biological Chemistry.

The evolution of long interspersed repeated DNA (L1, LINE 1) as revealed by the analysis of an ancient rodent L1 DNA family

A. Furano, K. Usdin, E. Pascale, 2006, Journal of Molecular Evolution.

Amplification of the ancient murine Lx family of long interspersed repeated DNA occurred during the murine radiation

P. Chevret, A. Furano, F. Catzeflis, 2004, Journal of Molecular Evolution.

Impaired activity-dependent FMRP translation and enhanced mGluR-dependent LTD in Fragile X premutation mice.

Adam J. Iliff, M. A. Sutton, P. Todd, 2013, Human molecular genetics.

Chromatin changes in the development and pathology of the Fragile X-associated disorders and Friedreich ataxia.

K. Usdin, R. Lokanga, Xiaonan Zhao, 2012, Biochimica et biophysica acta.

Ancient repeated DNA elements and the regulation of the human frataxin promoter.

E. Greene, K. Usdin, A. Entezam, 2005, Genomics.

CGG repeats associated with DNA instability and chromosome fragility form structures that block DNA synthesis in vitro.

K. Woodford, K. Usdin, 1995, Nucleic acids research.

Mismatch repair is a double-edged sword in the battle against microsatellite instability

K. Usdin, Carson Miller, 2022, Expert reviews in molecular medicine.

The role of DNA damage response pathways in chromosome fragility in Fragile X syndrome

A. Nakamura, W. Bonner, K. Usdin, 2009, Nucleic acids research.

Repeat-induced epigenetic changes in intron 1 of the frataxin gene and its consequences in Friedreich ataxia

E. Greene, K. Usdin, A. Entezam, 2007, Nucleic acids research.

The ability to form intrastrand tetraplexes is an evolutionarily conserved feature of the 3' end of L1 retrotransposons.

K. Usdin, R. Howell, 1997, Molecular biology and evolution.

Nucleic Acid Structures and the Transcription Defects in Fragile X Syndrome and Friedreich’s Ataxia

K. Usdin, 2005 .

L1 (LINE-1) retrotransposable elements provide a "fossil" record of the phylogenetic history of murid rodents.

P. Chevret, A. Furano, F. Catzeflis, 1995, Molecular biology and evolution.

Rapid evolution of a young L1 (LINE-1) clade in recently speciated rattus taxa

A. Furano, E. Cabot, K. Usdin, 1997, Journal of Molecular Evolution.

Chromosome fragility and the abnormal replication of the FMR1 locus in fragile X syndrome.

M. Aladjem, B. Hayward, K. Usdin, 2014, Human molecular genetics.

Repeat expansions confer WRN dependence in microsatellite-unstable cancers

K. Garimella, S. West, P. Meltzer, 2020, Nature.

The Repeat Expansion Diseases: The dark side of DNA repair.

K. Usdin, Xiaonan Zhao, 2015, DNA repair.

Repeat instability during DNA repair: Insights from model systems

K. Usdin, C. Freudenreich, N. House, 2015, Critical reviews in biochemistry and molecular biology.

Usdin repeat expansion diseases The biological effects of simple tandem repeats : Lessons from the

K. Usdin, 2008 .

The AUUCU Repeats Responsible for Spinocerebellar Ataxia Type 10 Form Unusual RNA Hairpins*

H. Yeh, P. McPhie, K. Usdin, 2005, Journal of Biological Chemistry.

Fragile X syndrome and Friedreich’s ataxia: two different paradigms for repeat induced transcript insufficiency

K. Usdin, E. Grabczyk, D. Kumari, 2001, Brain Research Bulletin.

DNA "Fossils" and Phylogenetic Analysis

A. Furano, K. Usdin, 1995, The Journal of Biological Chemistry.

Interaction of the Transcription Factors USF1, USF2, and α-Pal/Nrf-1 with the FMR1 Promoter

K. Usdin, D Kumari, K Usdin, 2001, The Journal of Biological Chemistry.

Repeat-mediated epigenetic dysregulation of the FMR1 gene in the fragile X-related disorders

K. Usdin, D. Kumari, 2015, Front. Genet..

Ovarian Abnormalities in a Mouse Model of Fragile X Primary Ovarian Insufficiency

J. Flaws, J. McDonald, L. Nelson, 2012, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Potassium bromate, a potent DNA oxidizing agent, exacerbates germline repeat expansion in a fragile X premutation mouse model

W. Le, K. Usdin, A. Entezam, 2010, Human mutation.

ATR protects the genome against CGG·CCG-repeat expansion in Fragile X premutation mice

K. Usdin, A. Entezam, 2007, Nucleic acids research.

The distribution of repressive histone modifications on silenced FMR1 alleles provides clues to the mechanism of gene silencing in fragile X syndrome.

K. Usdin, D. Kumari, 2010, Human molecular genetics.

Chromatin Remodeling in the Noncoding Repeat Expansion Diseases*

K. Usdin, D. Kumari, 2009, Journal of Biological Chemistry.

Interaction of the Transcription Factors USF1, USF2, and α-Pal/Nrf-1 with the FMR1 Promoter

K. Usdin, D. Kumari, 2001, The Journal of Biological Chemistry.

Small Molecules Targeting H3K9 Methylation Prevent Silencing of Reactivated FMR1 Alleles in Fragile X Syndrome Patient Derived Cells

K. Usdin, D. Kumari, Nicholas Sciascia, 2020, Genes.

Is Friedreich ataxia an epigenetic disorder?

K. Usdin, D. Kumari, 2012, Clinical Epigenetics.

Model systems for understanding FXPOI

S. Sherman, R. Hukema, K. Usdin, 2016 .

Transcription defects induced by repeat expansion: fragile X syndrome, FRAXE mental retardation, progressive myoclonus epilepsy type 1, and Friedreich ataxia

E. Greene, K. Usdin, D. Kumari, 2003, Cytogenetic and Genome Research.

The loss of a large DNA fragment is associated with an aerial mycelium negative (Amy-) phenotype of Streptomyces cattleya.

R. Kirby, C. Shaw, K. Usdin, 1985, Journal of general microbiology.

ATM and ATR protect the genome against two different types of tandem repeat instability in Fragile X premutation mice

K. Usdin, A. Entezam, 2009, Nucleic acids research.

Linking Dynamic DNA Secondary Structures to Genome Instability

S. Mirkin, A. Nussenzweig, A. Ansari, 2022, bioRxiv.

Common Threads: Aphidicolin-Inducible and Folate-Sensitive Fragile Sites in the Human Genome

K. Usdin, R. Lokanga, D. Kumari, 2021, Frontiers in Genetics.

Long uninterrupted CGG repeats within the first exon of the human FMR1 gene are not intrinsically unstable in transgenic mice.

R. Nussbaum, C. Lavedan, K. Usdin, 1998, Genomics.

SIRT1 Inhibition Alleviates Gene Silencing in Fragile X Mental Retardation Syndrome

K. Usdin, D. Kumari, R. Biacsi, 2008, PLoS genetics.

Alleviating transcript insufficiency caused by Friedreich's ataxia triplet repeats.

K. Usdin, E. Grabczyk, Karen Usdin, 2000, Nucleic acids research.

Pharmacological Reactivation of the Silenced FMR1 Gene as a Targeted Therapeutic Approach for Fragile X Syndrome

K. Usdin, I. Gazy, D. Kumari, 2019, Brain sciences.

Epigenetic dysregulation in the fragile X-related disorders

K. Usdin, D. Kumari, 2019, Chromatin Signaling and Neurological Disorders.

Repeat-mediated genetic and epigenetic changes at the FMR1 locus in the Fragile X-related disorders

B. Hayward, K. Usdin, R. Lokanga, 2014, Front. Genet..

The multiple molecular facets of fragile X-associated tremor/ataxia syndrome

F. Tassone, V. Peschansky, C. Pastori, 2014, Journal of Neurodevelopmental Disorders.

Mouse models of the fragile X premutation and fragile X-associated tremor/ataxia syndrome

D. Nelson, R. Willemsen, I. Pessah, 2014, Journal of Neurodevelopmental Disorders.

Linear plasmid vector for cloning of repetitive or unstable sequences in Escherichia coli

D. Mead, N. Ravin, A. Karsi, 2009, Nucleic acids research.

Mouse models of the fragile X premutation and fragile X-associated tremor/ataxia syndrome

Dalyir I. Pretto, R. Willemsen, I. Pessah, 2014, Journal of Neurodevelopmental Disorders.

A mouse model of the fragile X premutation: Effects on behavior, dendrite morphology, and regional rates of cerebral protein synthesis

C. B. Smith, G. Hoffman, K. Usdin, 2011, Neurobiology of Disease.

Regional FMRP deficits and large repeat expansions into the full mutation range in a new Fragile X premutation mouse model.

R. Nussbaum, K. Usdin, A. Entezam, 2007, Gene.

Long CGG‐repeat tracts are toxic to human cells: Implications for carriers of Fragile X premutation alleles

M. Cam, K. Usdin, D. Stiles, 2005, FEBS letters.

(Dys)function Follows Form: Nucleic Acid Structure, Repeat Expansion, and Disease Pathology in FMR1 Disorders

K. Usdin, Xiaonan Zhao, 2021, International journal of molecular sciences.

Mechanisms of Genome Instability in the Fragile X-Related Disorders

B. Hayward, K. Usdin, 2021, Genes.

Polycomb group complexes are recruited to reactivated FMR1 alleles in Fragile X syndrome in response to FMR1 transcription.

K. Usdin, D. Kumari, 2014, Human molecular genetics.

Repeat Expansion Affects Both Transcription Initiation and Elongation in Friedreich Ataxia Cells*

K. Usdin, D. Kumari, R. Biacsi, 2010, The Journal of Biological Chemistry.

Current Issues and Therapeutic Prospects

M. Fry, K. Usdin, 2006 .

The structure of the guanine-rich polypurine:polypyrimidine sequence at the right end of the rat L1 (LINE) element.

A. Furano, K. Usdin, Karen Usdin, 1989, The Journal of biological chemistry.

DNA Secondary Structures and the Evolution of Hypervariable Tandem Arrays*

K. Woodford, Karen Usdin, K. Usdin, 1997, The Journal of Biological Chemistry.

The use of K(+)-free buffers eliminates a common cause of premature chain termination in PCR and PCR sequencing.

K. Woodford, K. Usdin, M. Weitzmann, 1995, Nucleic acids research.

Evidence for chromosome fragility at the frataxin locus in Friedreich ataxia.

A. Nakamura, W. Bonner, B. Hayward, 2015, Mutation research.

The GAA*TTC triplet repeat expanded in Friedreich's ataxia impedes transcription elongation by T7 RNA polymerase in a length and supercoil dependent manner.

K. Usdin, E. Grabczyk, Karen Usdin, 2000, Nucleic acids research.

Timing of Expansion of Fragile X Premutation Alleles During Intergenerational Transmission in a Mouse Model of the Fragile X-Related Disorders

K. Usdin, Xiaonan Zhao, 2018, Front. Genet..

Modifiers of Somatic Repeat Instability in Mouse Models of Friedreich Ataxia and the Fragile X-Related Disorders: Implications for the Mechanism of Somatic Expansion in Huntington’s Disease

Carson J Miller, B. Hayward, R. M. Pinto, 2021, Journal of Huntington's disease.

Isolation and Analysis of the CGG-Repeat Size in Male and Female Gametes from a Fragile X Mouse Model.

P. Dagur, K. Usdin, Xiaonan Zhao, 2019, Methods in molecular biology.

Repeat Instability in the Fragile X-Related Disorders: Lessons from a Mouse Model

F. Tassone, B. Hayward, K. Usdin, 2019, Brain sciences.

A Set of Assays for the Comprehensive Analysis of FMR1 Alleles in the Fragile X-Related Disorders.

B. Hayward, Yifan Zhou, K. Usdin, 2016, The Journal of molecular diagnostics : JMD.

Mutsβ generates both expansions and contractions in a mouse model of the Fragile X-associated disorders.

Wei Yang, K. Usdin, Xiaonan Zhao, 2015, Human molecular genetics.

Gender and Cell‐Type‐Specific Effects of the Transcription‐Coupled Repair Protein, ERCC6/CSB, on Repeat Expansion in a Mouse Model of the Fragile X‐Related Disorders

K. Usdin, Xiaonan Zhao, 2014, Human mutation.

DNA repeat expansions and human disease

K. Usdin, E. Grabczyk, 2000, Cellular and Molecular Life Sciences CMLS.

The roles of Sp1, Sp3, USF1/USF2 and NRF-1 in the regulation and three-dimensional structure of the Fragile X mental retardation gene promoter.

A. Gabrielian, David Wheeler, K. Usdin, 2005, The Biochemical journal.

Mechanisms of Repeat Instability in Fragile X Syndrome

K. Usdin, Xiaonan Zhao, I. Gazy, 2017 .

Ups and Downs: Mechanisms of Repeat Instability in the Fragile X-Related Disorders

K. Usdin, Xiaonan Zhao, 2016, Genes.

The fragile X syndrome repeats form RNA hairpins that do not activate the interferon-inducible protein kinase, PKR, but are cut by Dicer.

K. Usdin, Tapas Saha, V. Handa, 2003, Nucleic acids research.

Recent advances in assays for the fragile X-related disorders

B. Hayward, K. Usdin, D. Kumari, 2017, Human Genetics.

Generation of microgram quantities of trinucleotide repeat tracts of defined length, interspersion pattern, and orientation.

K. Usdin, E. Grabczyk, 1999, Analytical biochemistry.

When secondary comes first--the importance of non-canonical DNA structures.

N. Saini, Yu Zhang, K. Lobachev, 2013, Biochimie.

The isolation and restriction mapping of a miniplasmid from the Actinomycete Nocardia corallina

R. Kirby, K. Usdin, 1985 .

Sustained expression of FMR1 mRNA from reactivated fragile X syndrome alleles after treatment with small molecules that prevent trimethylation of H3K27.

K. Usdin, D. Kumari, 2016, Human molecular genetics.

Sustained expression of FMR 1 mRNA from reactivated fragile X syndrome alleles after treatment with small molecules that prevent trimethylation of H 3 K 27

K. Usdin, D. Kumari, 2016 .

A point mutation in the nuclease domain of MLH3 eliminates repeat expansions in a mouse stem cell model of the Fragile X-related disorders.

B. Hayward, K. Usdin, P. Steinbach, 2020, Nucleic acids research.

All three mammalian MutL complexes are required for repeat expansion in a mouse cell model of the Fragile X-related disorders

Carson J Miller, K. Usdin, Xiaonan Zhao, 2020, PLoS genetics.

High‐Throughput Screening to Identify Compounds That Increase Fragile X Mental Retardation Protein Expression in Neural Stem Cells Differentiated From Fragile X Syndrome Patient‐Derived Induced Pluripotent Stem Cells

Wenwei Huang, Noel Southall, Wei Zheng, 2015, Stem cells translational medicine.

Double-strand break repair plays a role in repeat instability in a fragile X mouse model.

Svetlana Potapova, B. Hayward, K. Usdin, 2019, DNA repair.

Repeat expansions nested within tandem CNVs: A unique structural change in GLS exemplifies the diagnostic challenges of non-coding pathogenic variation.

Undiagnosed Diseases Network, S. Züchner, A. V. van Kuilenburg, 2022, Human molecular genetics.

Clinical implications of somatic allele expansion in female FMR1 premutation carriers

F. Tassone, B. Durbin-Johnson, R. Hagerman, 2023, Scientific reports.

The Mouse Ms6-hm Hypervariable Microsatellite Forms a Hairpin and Two Unusual Tetraplexes*

K. Woodford, K. Usdin, M. Weitzmann, 1998, The Journal of Biological Chemistry.

Muts Beta-dependent Contribution Of Muts Alpha To Repeat Expansions In Fragile X Premutation Mice?

K. Allette, K. Usdin, R. Lokanga, 2016 .

FAN1's protection against CGG repeat expansion requires its nuclease activity and is FANCD2-independent.

K. Usdin, Xiaonan Zhao, Huiyan Lu, 2021, Nucleic acids research.

Editorial: Proceedings of the “Fourth International Conference of the FMR1 Premutation: Basic Mechanisms, Clinical Involvement and Therapy”

C. Giulivi, R. Willemsen, R. Hukema, 2021, Frontiers in Molecular Biosciences.

Glutaminase Deficiency Caused by Short Tandem Repeat Expansion in GLS. Reply.

A. V. van Kuilenburg, C. V. van Karnebeek, K. Usdin, 2019, The New England journal of medicine.

NF-Y, AP2, Nrf1 and Sp1 regulate the fragile X-related gene 2 (FXR2).

Karen Usdin, K. Usdin, Lata Mahishi, 2006, The Biochemical journal.

Activation Ratio Correlates with IQ in Female Carriers of the FMR1 Premutation

F. Tassone, B. Durbin-Johnson, R. Hagerman, 2023, Cells.

Is Friedreich ataxia an epigenetic disorder?

K. Usdin, D. Kumari, 2012, Clinical Epigenetics.

Mouse models of the fragile X premutation and fragile X-associated tremor/ataxia syndrome

D. Nelson, R. Willemsen, I. Pessah, 2014, Journal of Neurodevelopmental Disorders.

Insertion of L1 elements into sites that can form non-B DNA. Interactions of non-B DNA-forming sequences.

A. Furano, K. Usdin, 1989, The Journal of biological chemistry.

Sequencing errors in reactions using labeled terminators.

K. Usdin, D. Kumari, 1999, BioTechniques.

Impaired activity-dependent FMRP translation and enhanced mGluR-dependent LTD in Fragile X premutation mice.

Peter K. Todd, Adam J. Iliff, M. A. Sutton, 2013, Human molecular genetics.

The Repeat Expansion Diseases: The dark side of DNA repair.

K. Usdin, Xiaonan Zhao, 2015, DNA Repair.

DIP2B CGG repeat expansion in siblings with neurodevelopmental disability and progressive movement disorder

K. Usdin, C. Karnebeek, Canada Consortium, 2024, medRxiv.

All three MutL complexes are required for repeat expansion in a human stem cell model of CAG-repeat expansion mediated glutaminase deficiency

K. Usdin, D. Kumari, Bruce Hayward, 2024, bioRxiv.