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FRIZZY PANICLE drives supernumerary spikelets in bread wheat

Plant physiology (Bethesda), 2015-01, Vol.167 (1), p.189-199

2015

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Correlation between Density of CD8+ T-cell Infiltrate in Microsatellite Unstable Colorectal Cancers and Frameshift Mutations: A Rationale for Personalized Immunotherapy

Cancer research (Chicago, Ill.), 2015-09, Vol.75 (17), p.3446-3455

2015

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Precise therapeutic gene correction by a simple nuclease-induced double-stranded break

Nature (London), 2019-04, Vol.568 (7753), p.561-565

2019

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Clinically Relevant Correction of Recessive Dystrophic Epidermolysis Bullosa by Dual sgRNA CRISPR/Cas9-Mediated Gene Editing

Molecular therapy, 2019-05, Vol.27 (5), p.986-998

2019

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Activation of WNT/β‐catenin signaling results in resistance to a dual PI3K/mTOR inhibitor in colorectal cancer cells harboring PIK3CA mutations

International journal of cancer, 2019-01, Vol.144 (2), p.389-401

2019

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Mutations in SLC30A10 Cause Parkinsonism and Dystonia with Hypermanganesemia, Polycythemia, and Chronic Liver Disease

American journal of human genetics, 2012-03, Vol.90 (3), p.467-477

2012

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Functional Rescue of Dystrophin Deficiency in Mice Caused by Frameshift Mutations Using Campylobacter jejuni Cas9

Molecular therapy, 2018-06, Vol.26 (6), p.1529-1538

2018

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Homopolymer switches mediate adaptive mutability in mismatch repair-deficient colorectal cancer

Nature genetics, 2024-07, Vol.56 (7), p.1420-1433

2024

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Loss of Function of the Nuclear Receptor NR2F2, Encoding COUP-TF2, Causes Testis Development and Cardiac Defects in 46,XX Children

American journal of human genetics, 2018-03, Vol.102 (3), p.487-493

2018

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Complex dynamics under tension in a high-efficiency frameshift stimulatory structure

Proceedings of the National Academy of Sciences - PNAS, 2019-09, Vol.116 (39), p.19500-19505

2019

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Knockout of the HMG domain of the porcine SRY gene causes sex reversal in gene-edited pigs

Proceedings of the National Academy of Sciences - PNAS, 2021-01, Vol.118 (2), p.1-9

2021

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Antibiotic resistance by high-level intrinsic suppression of a frameshift mutation in an essential gene

Proceedings of the National Academy of Sciences - PNAS, 2020-02, Vol.117 (6), p.3185-3191

2020

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A rare frameshift mutation in the AGPAT2 gene in a family from gaza with congenital generalized lipodystrophy

Clinical endocrinology (Oxford), 2020-08, Vol.93 (2), p.212-214

2020

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Homozygous frameshift variant in desmoglein 2 gene causes biventricular arrhythmogenic right ventricular cardiomyopathy

Clinical genetics, 2023-08, Vol.104 (2), p.266-268

2023

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CCDC82 frameshift mutation associated with intellectual disability, spastic paraparesis, and dysmorphic features

Clinical genetics, 2022-07, Vol.102 (1), p.80-81

2022

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Novel PATL2 variants cause female infertility with oocyte maturation defect

Journal of assisted reproduction and genetics, 2024-08, Vol.41 (8), p.1965-1976

2024

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Tumor-Infiltrating T Cells From Clear Cell Renal Cell Carcinoma Patients Recognize Neoepitopes Derived From Point and Frameshift Mutations

Frontiers in immunology, 2020-03, Vol.11, p.373-373

2020

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Genetic Control of Seed Shattering in Rice by the APETALA2 Transcription Factor SHATTERING ABORTION1

The Plant cell, 2012-03, Vol.24 (3), p.1034-1048

2012

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Gamma knife radiotherapy in a neurofibromatosis type 1 Chinese pedigrees with NF1 gene frameshift mutation: A case report

Medicine (Baltimore), 2022-07, Vol.101 (27), p.e29280-e29280

2022

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A pathogenic DMC1 frameshift mutation causes nonobstructive azoospermia but not primary ovarian insufficiency in humans

Molecular human reproduction, 2021-09, Vol.27 (9)

2021

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Phenotypic expansion of Bosch–Boonstra–Schaaf optic atrophy syndrome and further evidence for genotype–phenotype correlations

American journal of medical genetics. Part A, 2020-06, Vol.182 (6), p.1426-1437

2020

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A single regulatory gene is sufficient to alter Vibrio aestuarianus pathogenicity in oysters

Environmental microbiology, 2015-11, Vol.17 (11), p.4189-4199

2015

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Whole‐exome sequencing identified a novel frameshift mutation in SDR9C7 underlying autosomal recessive congenital ichthyosis in a Pakistani family

British journal of dermatology (1951), 2017-11, Vol.177 (5), p.e191-e192

2017

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PHIP gene variants with protein modeling, interactions, and clinical phenotypes

American journal of medical genetics. Part A, 2022-02, Vol.188 (2), p.579-589

2022

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FRIZZY PANICLE drives supernumerary spikelets in bread wheat

Correlation between Density of CD8+ T-cell Infiltrate in Microsatellite Unstable Colorectal Cancers and Frameshift Mutations: A Rationale for Personalized Immunotherapy

Precise therapeutic gene correction by a simple nuclease-induced double-stranded break

Clinically Relevant Correction of Recessive Dystrophic Epidermolysis Bullosa by Dual sgRNA CRISPR/Cas9-Mediated Gene Editing

Activation of WNT/β‐catenin signaling results in resistance to a dual PI3K/mTOR inhibitor in colorectal cancer cells harboring PIK3CA mutations

Mutations in SLC30A10 Cause Parkinsonism and Dystonia with Hypermanganesemia, Polycythemia, and Chronic Liver Disease

Functional Rescue of Dystrophin Deficiency in Mice Caused by Frameshift Mutations Using Campylobacter jejuni Cas9

Homopolymer switches mediate adaptive mutability in mismatch repair-deficient colorectal cancer

Loss of Function of the Nuclear Receptor NR2F2, Encoding COUP-TF2, Causes Testis Development and Cardiac Defects in 46,XX Children

Complex dynamics under tension in a high-efficiency frameshift stimulatory structure

Knockout of the HMG domain of the porcine SRY gene causes sex reversal in gene-edited pigs

Antibiotic resistance by high-level intrinsic suppression of a frameshift mutation in an essential gene

A rare frameshift mutation in the AGPAT2 gene in a family from gaza with congenital generalized lipodystrophy

Homozygous frameshift variant in desmoglein 2 gene causes biventricular arrhythmogenic right ventricular cardiomyopathy

Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in mice

CCDC82 frameshift mutation associated with intellectual disability, spastic paraparesis, and dysmorphic features

Novel PATL2 variants cause female infertility with oocyte maturation defect

Tumor-Infiltrating T Cells From Clear Cell Renal Cell Carcinoma Patients Recognize Neoepitopes Derived From Point and Frameshift Mutations

Genetic Control of Seed Shattering in Rice by the APETALA2 Transcription Factor SHATTERING ABORTION1

Gamma knife radiotherapy in a neurofibromatosis type 1 Chinese pedigrees with NF1 gene frameshift mutation: A case report

A pathogenic DMC1 frameshift mutation causes nonobstructive azoospermia but not primary ovarian insufficiency in humans

Phenotypic expansion of Bosch–Boonstra–Schaaf optic atrophy syndrome and further evidence for genotype–phenotype correlations

A single regulatory gene is sufficient to alter Vibrio aestuarianus pathogenicity in oysters

Whole‐exome sequencing identified a novel frameshift mutation in SDR9C7 underlying autosomal recessive congenital ichthyosis in a Pakistani family

PHIP gene variants with protein modeling, interactions, and clinical phenotypes

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