| 1 | One Shock, Not One Cure: Electroporation Reveals Disease-Specific Constraints in Hepatocyte Gene Editing Therapy | 2.2 | 1 | Citations (PDF) |
| 2 | Complete correction of murine phenylketonuria by selection-enhanced hepatocyte transplantation | 9.6 | 12 | Citations (PDF) |
| 3 | Long‐term combination therapy with metformin and oxymetholone in a Fanconi anemia mouse model | 0.9 | 2 | Citations (PDF) |
| 4 | In vivo selection of hepatocytes | 9.6 | 5 | Citations (PDF) |
| 5 | Rapid in vivo multiplexed editing (RIME) of the adult mouse liver | 9.6 | 10 | Citations (PDF) |
| 6 | A DNA methylation atlas of normal human cell types | 30.6 | 631 | Citations (PDF) |
| 7 | Replication stress increases mitochondrial metabolism and mitophagy in FANCD2 deficient fetal liver hematopoietic stem cells | 1.7 | 6 | Citations (PDF) |
| 8 | Strong ubiquitous micro-promoters for recombinant adeno-associated viral vectors | 3.0 | 27 | Citations (PDF) |
| 9 | In vivo tracing of the Cytokeratin 14 lineages using self-cleaving guide RNAs and CRISPR/Cas9 | 1.3 | 0 | Citations (PDF) |
| 10 | Development of a Beta Cell-Specific Expression Control Element for Recombinant Adeno-Associated Virus | 2.3 | 3 | Citations (PDF) |
| 11 | Self-cleaving guide RNAs enable pharmacological selection of precise gene editing events in vivo | 10.8 | 13 | Citations (PDF) |
| 12 | Induced Liver Regeneration Enhances CRISPR/Cas9-Mediated Gene Repair in Tyrosinemia Type 1 | 2.3 | 18 | Citations (PDF) |
| 13 | MYC Promotes Bone Marrow Stem Cell Dysfunction in Fanconi Anemia | 11.6 | 52 | Citations (PDF) |
| 14 | Inhibition of TGFβ1 and TGFβ3 promotes hematopoiesis in Fanconi anemia | 0.6 | 21 | Citations (PDF) |
| 15 | Liver Injury Increases the Incidence of HCC following AAV Gene Therapy in Mice | 6.0 | 99 | Citations (PDF) |
| 16 | Proliferative polyploid cells give rise to tumors via ploidy reduction | 10.8 | 92 | Citations (PDF) |
| 17 | Therapeutic liver repopulation by transient acetaminophen selection of gene-modified hepatocytes | 8.7 | 32 | Citations (PDF) |
| 18 | Dynamic Transcriptional and Epigenetic Changes Drive Cellular Plasticity in the Liver | 9.6 | 44 | Citations (PDF) |
| 19 | Liver-humanized mice fed a NASH-diet are an advanced model to study cardiometabolic diseases | 1.9 | 0 | Citations (PDF) |
| 20 | AAV integration in human hepatocytes | 6.0 | 125 | Citations (PDF) |
| 21 | In vitro expansion of cirrhosis derived liver epithelial cells with defined small molecules | 0.3 | 8 | Citations (PDF) |
| 22 | The Significance of Polyploid Hepatocytes During Aging Process | 4.0 | 22 | Citations (PDF) |
| 23 | Generation of functional ciliated cholangiocytes from human pluripotent stem cells | 10.8 | 40 | Citations (PDF) |
| 24 | AAV-Mediated CRISPR/Cas9 Gene Editing in Murine Phenylketonuria | 3.0 | 91 | Citations (PDF) |
| 25 | In Vivo Lineage Tracing of Polyploid Hepatocytes Reveals Extensive Proliferation during Liver Regeneration | 11.6 | 178 | Citations (PDF) |
| 26 | Insights From Liver‐Humanized Mice on Cholesterol Lipoprotein Metabolism and LXR‐Agonist Pharmacodynamics in Humans | 9.6 | 39 | Citations (PDF) |
| 27 | Efficient in vivo editing of OTC-deficient patient-derived primary human hepatocytes | 3.1 | 25 | Citations (PDF) |
| 28 | Endoplasmic Reticulum Stress-Induced Upregulation of STARD1 Promotes Acetaminophen-Induced Acute Liver Failure | 0.9 | 127 | Citations (PDF) |
| 29 | Diabetes relief in mice by glucose-sensing insulin-secreting human α-cells | 30.6 | 242 | Citations (PDF) |
| 30 | Loss of Oxidation Resistance 1, OXR1, Is Associated with an Autosomal-Recessive Neurological Disease with Cerebellar Atrophy and Lysosomal Dysfunction | 4.0 | 59 | Citations (PDF) |
| 31 | Combination therapy with atorvastatin and celecoxib delays tumor formation in a Fanconi anemia mouse model | 0.9 | 8 | Citations (PDF) |
| 32 | Using a barcoded AAV capsid library to select for clinically relevant gene therapy vectors | 3.7 | 95 | Citations (PDF) |
| 33 | Long-Term Correction of Diabetes in Mice by In Vivo Reprogramming of Pancreatic Ducts | 6.0 | 30 | Citations (PDF) |
| 34 | Bioengineered AAV Capsids with Combined High Human Liver Transduction In Vivo and Unique Humoral Seroreactivity | 6.0 | 164 | Citations (PDF) |
| 35 | Monitoring liver damage using hepatocyte-specific methylation markers in cell-free circulating DNA | 3.7 | 132 | Citations (PDF) |
| 36 | Inflammatory Cytokine TNFα Promotes the Long-Term Expansion of Primary Hepatocytes in 3D CultureCell, 2018, 175, 1607-1619.e15 | 23.4 | 322 | Citations (PDF) |
| 37 | Comprehensive human cell-type methylation atlas reveals origins of circulating cell-free DNA in health and disease | 10.8 | 976 | Citations (PDF) |
| 38 | A Drug Screen using Human iPSC-Derived Hepatocyte-like Cells Reveals Cardiac Glycosides as a Potential Treatment for Hypercholesterolemia | 11.6 | 106 | Citations (PDF) |
| 39 | Diagnosis and treatment of tyrosinemia type I: a US and Canadian consensus group review and recommendations | 3.3 | 224 | Citations (PDF) |
| 40 | Glycoprotein 2 is a specific cell surface marker of human pancreatic progenitors | 10.8 | 145 | Citations (PDF) |
| 41 | Genome-wide genetic and epigenetic analyses of pancreatic acinar cell carcinomas reveal aberrations in genome stability | 10.8 | 70 | Citations (PDF) |
| 42 | Adult Mouse Liver Contains Two Distinct Populations of Cholangiocytes | 3.0 | 79 | Citations (PDF) |
| 43 | Chronic Phenotype Characterization of a Large-Animal Model of Hereditary Tyrosinemia Type 1 | 2.8 | 20 | Citations (PDF) |
| 44 | Reprogramming human gallbladder cells into insulin-producing β-like cells | 1.5 | 39 | Citations (PDF) |
| 45 | Metformin improves defective hematopoiesis and delays tumor formation in Fanconi anemia miceBlood, 2016, 128, 2774-2784 | 3.6 | 73 | Citations (PDF) |
| 46 | Efficient generation of pancreatic β-like cells from the mouse gallbladder | 0.3 | 14 | Citations (PDF) |
| 47 | Age-Dependent Pancreatic Gene Regulation Reveals Mechanisms Governing Human β Cell Function | 20.8 | 244 | Citations (PDF) |
| 48 | Single-Cell Mass Cytometry Analysis of the Human Endocrine Pancreas | 20.8 | 165 | Citations (PDF) |
| 49 | Stem Cells and Regeneration in the Digestive System: Keystone Meeting | 0.9 | 0 | Citations (PDF) |
| 50 | Silent Tyrosinemia Type I Without Elevated Tyrosine or Succinylacetone Associated with Liver Cirrhosis and Hepatocellular Carcinoma | 1.0 | 32 | Citations (PDF) |
| 51 | Curative ex vivo liver-directed gene therapy in a pig model of hereditary tyrosinemia type 1 | 8.7 | 69 | Citations (PDF) |
| 52 | A universal system to select gene-modified hepatocytes in vivo | 8.7 | 43 | Citations (PDF) |
| 53 | Human islets contain four distinct subtypes of β cells | 10.8 | 377 | Citations (PDF) |
| 54 | TGF-β Inhibition Rescues Hematopoietic Stem Cell Defects and Bone Marrow Failure in Fanconi Anemia | 11.6 | 152 | Citations (PDF) |
| 55 | Stem cells versus plasticity in liver and pancreas regeneration | 12.6 | 168 | Citations (PDF) |
| 56 | Identification of tissue-specific cell death using methylation patterns of circulating DNA | 5.2 | 590 | Citations (PDF) |
| 57 | The Sirt1 activator SRT3025 expands hematopoietic stem and progenitor cells and improves hematopoiesis in Fanconi anemia mice | 0.3 | 27 | Citations (PDF) |
| 58 | Fibroblast Growth Factor Signaling Controls Liver Size in Mice With Humanized Livers | 0.9 | 109 | Citations (PDF) |
| 59 | Oxymetholone Therapy of Fanconi Anemia Suppresses Osteopontin Transcription and Induces Hematopoietic Stem Cell Cycling | 3.0 | 32 | Citations (PDF) |
| 60 | Directed differentiation of cholangiocytes from human pluripotent stem cells | 19.7 | 311 | Citations (PDF) |
| 61 | Novel surface markers directed against adult human gallbladder | 0.3 | 7 | Citations (PDF) |
| 62 | Genome editing with Cas9 in adult mice corrects a disease mutation and phenotype | 19.7 | 891 | Citations (PDF) |
| 63 | Pharmacologic inhibition of L‐tyrosine degradation ameliorates cerebral dopamine deficiency in murine phenylketonuria (PKU) | 2.6 | 47 | Citations (PDF) |
| 64 | Extensive double humanization of both liver and hematopoiesis in FRGN mice | 0.3 | 136 | Citations (PDF) |
| 65 | Bipotential Adult Liver Progenitors Are Derived from Chronically Injured Mature Hepatocytes | 11.6 | 510 | Citations (PDF) |
| 66 | The organoid-initiating cells in mouse pancreas and liver are phenotypically and functionally similar | 0.3 | 76 | Citations (PDF) |
| 67 | Clonal Tracing of Sox9+ Liver Progenitors in Mouse Oval Cell Injury | 9.6 | 214 | Citations (PDF) |
| 68 | Fumarylacetoacetate hydrolase deficient pigs are a novel large animal model of metabolic liver disease | 0.3 | 64 | Citations (PDF) |
| 69 | Human pancreatic cancer fusion 2 (HPC2) 1‐B3: A novel monoclonal antibody to screen for pancreatic ductal dysplasia | 1.3 | 3 | Citations (PDF) |
| 70 | Response to “Can ‘humanized’ mice improve drug development in the 21st century?” | 8.2 | 5 | Citations (PDF) |
| 71 | Generation of islet-like cells from mouse gall bladder by direct ex vivo reprogramming | 0.3 | 46 | Citations (PDF) |
| 72 | Anthracyclines Induce DNA Damage Response-Mediated Protection against Severe Sepsis | 16.6 | 145 | Citations (PDF) |
| 73 | New potential cell source for hepatocyte transplantation: Discarded livers from metabolic disease liver transplants | 0.3 | 58 | Citations (PDF) |
| 74 | Mice With Human Livers | 0.9 | 136 | Citations (PDF) |
| 75 | Fancd2 and p21 function independently in maintaining the size of hematopoietic stem and progenitor cell pool in mice | 0.3 | 12 | Citations (PDF) |
| 76 | p53 regulates a mitotic transcription program and determines ploidy in normal mouse liver | 9.6 | 93 | Citations (PDF) |
| 77 | In vitro expansion of single Lgr5+ liver stem cells induced by Wnt-driven regeneration | 30.6 | 1,529 | Citations (PDF) |
| 78 | Epigenomic plasticity enables human pancreatic α to β cell reprogramming | 6.6 | 399 | Citations (PDF) |
| 79 | Mice with Chimeric Livers Are an Improved Model for Human Lipoprotein Metabolism | 1.5 | 50 | Citations (PDF) |
| 80 | Selection and evaluation of clinically relevant AAV variants in a xenograft liver model | 30.6 | 443 | Citations (PDF) |
| 81 | AAV Vectors Containing rDNA Homology Display Increased Chromosomal Integration and Transgene Persistence | 6.0 | 45 | Citations (PDF) |
| 82 | In Vivo Selection of Transplanted Hepatocytes by Pharmacological Inhibition of Fumarylacetoacetate Hydrolase in Wild-type Mice | 6.0 | 17 | Citations (PDF) |
| 83 | Ribosomal DNA Integrating rAAV-rDNA Vectors Allow for Stable Transgene Expression | 6.0 | 34 | Citations (PDF) |
| 84 | Frequent Aneuploidy Among Normal Human Hepatocytes | 0.9 | 197 | Citations (PDF) |
| 85 | AAV-Mediated Gene Targeting Is Significantly Enhanced by Transient Inhibition of Nonhomologous End Joining or the Proteasome
In Vivo | 2.3 | 35 | Citations (PDF) |
| 86 | Bone Marrow Failure in Fanconi Anemia Is Triggered by an Exacerbated p53/p21 DNA Damage Response that Impairs Hematopoietic Stem and Progenitor Cells | 11.6 | 310 | Citations (PDF) |
| 87 | The novel monoclonal antibody HPC2 and N-cadherin distinguish pancreatic ductal adenocarcinoma from cholangiocarcinoma | 1.7 | 22 | Citations (PDF) |
| 88 | Complete Plasmodium falciparum liver-stage development in liver-chimeric mice | 6.6 | 241 | Citations (PDF) |
| 89 | Aneuploidy as a mechanism for stress-induced liver adaptation | 6.6 | 161 | Citations (PDF) |
| 90 | Isolation of mouse pancreatic alpha, beta, duct and acinar populations with cell surface markers | 2.0 | 50 | Citations (PDF) |
| 91 | Transcriptomes of the major human pancreatic cell types | 4.9 | 208 | Citations (PDF) |
| 92 | Efficient production of Fah -null heterozygote pigs by chimeric adeno-associated virus-mediated gene knockout and somatic cell nuclear transfer | 9.6 | 79 | Citations (PDF) |
| 93 | Notch signaling inhibits hepatocellular carcinoma following inactivation of the RB pathway | 5.9 | 210 | Citations (PDF) |
| 94 | Foxl1-Cre-marked adult hepatic progenitors have clonogenic and bilineage differentiation potential | 2.8 | 145 | Citations (PDF) |
| 95 | Prospective isolation of a bipotential clonogenic liver progenitor cell in adult mice | 2.8 | 223 | Citations (PDF) |
| 96 | Fancd2
−/− mice have hematopoietic defects that can be partially corrected by resveratrolBlood, 2010, 116, 5140-5148 | 3.6 | 96 | Citations (PDF) |
| 97 | 106 IDENTIFICATION OF JOINT OCHRONOSIS IN A MOUSE MODEL OF ALKAPTONURIA | 3.0 | 0 | Citations (PDF) |
| 98 | Adeno‐associated virus gene repair corrects a mouse model of hereditary tyrosinemia in vivo†‡ | 9.6 | 130 | Citations (PDF) |
| 99 | The ploidy conveyor of mature hepatocytes as a source of genetic variation | 30.6 | 497 | Citations (PDF) |
| 100 | Non-Invasive Stem Cell Therapy in a Rat Model for Retinal Degeneration and Vascular Pathology | 1.5 | 134 | Citations (PDF) |
| 101 | Deficiencies in the Fanconi Anemia DNA Damage Response Pathway Increase Sensitivity to HPV-Associated Head and Neck Cancer | 2.6 | 89 | Citations (PDF) |
| 102 | Therapeutic Liver Reconstitution With Murine Cells Isolated Long After Death | 0.9 | 31 | Citations (PDF) |
| 103 | Chromosomal Integration of Adenoviral Vector DNA
In Vivo | 2.4 | 89 | Citations (PDF) |
| 104 | Validation of Fanconi anemia complementation Group A assignment using molecular analysis | 3.3 | 18 | Citations (PDF) |
| 105 | Ploidy Reductions in Murine Fusion-Derived Hepatocytes | 2.2 | 100 | Citations (PDF) |
| 106 | Embryonic Lethality after Combined Inactivation of
Fancd2
and
Mlh1
in Mice | 2.6 | 9 | Citations (PDF) |
| 107 | Generation of Monoclonal Antibodies Specific for Cell Surface Molecules Expressed on Early Mouse Endoderm | 2.7 | 39 | Citations (PDF) |
| 108 | CDX2 in the formation of the trophectoderm lineage in primate embryos | 1.3 | 38 | Citations (PDF) |
| 109 | Stem Cells and Liver Regeneration | 0.9 | 529 | Citations (PDF) |
| 110 | Activation of nuclear factor E2‐related factor 2 in hereditary tyrosinemia type 1 and its role in survival and tumor development† | 9.6 | 38 | Citations (PDF) |
| 111 | Surface markers for the murine oval cell response† | 9.6 | 88 | Citations (PDF) |
| 112 | CXCR4 induction in hematopoietic progenitor cells from Fanca−/−, -c−/−, and -d2−/− mice | 0.6 | 13 | Citations (PDF) |
| 113 | Loss of p21 Permits Carcinogenesis from Chronically Damaged Liver and Kidney Epithelial Cells despite Unchecked Apoptosis | 28.4 | 62 | Citations (PDF) |
| 114 | Signaling networks in hepatic oval cell activation | 0.3 | 53 | Citations (PDF) |
| 115 | Isolation of major pancreatic cell types and long-term culture-initiating cells using novel human surface markers | 0.3 | 116 | Citations (PDF) |
| 116 | ERCC1 is required for FANCD2 focus formation | 0.5 | 18 | Citations (PDF) |
| 117 | W1838 Development of Monoclonal Antibodies to Aid in the Diagnosis of Pancreatic Cancer | 0.9 | 0 | Citations (PDF) |
| 118 | Slow-onset inhibition of fumarylacetoacetate hydrolase by phosphinate mimics of the tetrahedral intermediate: kinetics, crystal structure and pharmacokinetics | 2.3 | 17 | Citations (PDF) |
| 119 | Hypomorphic Mutations in the Gene Encoding a Key Fanconi Anemia Protein, FANCD2, Sustain a Significant Group of FA-D2 Patients with Severe Phenotype | 4.0 | 132 | Citations (PDF) |
| 120 | Robust expansion of human hepatocytes in Fah−/−/Rag2−/−/Il2rg−/− mice | 19.7 | 819 | Citations (PDF) |
| 121 | Bone marrow-derived cells fuse with normal and transformed intestinal stem cells | 5.2 | 266 | Citations (PDF) |
| 122 | Sustained Phosphorylation of Bid Is a Marker for Resistance to Fas-Induced Apoptosis During Chronic Liver Diseases | 0.9 | 33 | Citations (PDF) |
| 123 | Natural gene therapy in monozygotic twins with Fanconi anemiaBlood, 2006, 107, 3084-3090 | 3.6 | 81 | Citations (PDF) |
| 124 | Principles of therapeutic liver repopulation | 2.6 | 53 | Citations (PDF) |
| 125 | Seeking Consensus: A Clarification and Defense of Altered Nuclear Transfer | 0.6 | 13 | Citations (PDF) |
| 126 | Myeloid lineage progenitors give rise to vascular endothelium | 5.2 | 189 | Citations (PDF) |
| 127 | In Vivo Genetic Selection of Renal Proximal Tubules | 6.0 | 60 | Citations (PDF) |
| 128 | Gene therapy of metachromatic leukodystrophy reverses neurological damage and deficits in mice | 6.6 | 219 | Citations (PDF) |
| 129 | Regulated interaction of the Fanconi anemia protein, FANCD2, with chromatinBlood, 2005, 105, 1003-1009 | 3.6 | 122 | Citations (PDF) |
| 130 | Liver Repair by Intra- and Extrahepatic Progenitors | 5.6 | 33 | Citations (PDF) |
| 131 | Large-Scale Molecular Characterization of Adeno-Associated Virus Vector Integration in Mouse Liver | 2.4 | 172 | Citations (PDF) |
| 132 | In Vivo Correction of Murine Hereditary Tyrosinemia Type I by ϕC31 Integrase-Mediated Gene Delivery | 6.0 | 131 | Citations (PDF) |
| 133 | Low Therapeutic Threshold for Hepatocyte Replacement in Murine Phenylketonuria | 6.0 | 63 | Citations (PDF) |
| 134 | Fancd2 functions in a double strand break repair pathway that is distinct from non-homologous end joining | 2.1 | 57 | Citations (PDF) |
| 135 | The Origin of Hepatocytes | 0.9 | 22 | Citations (PDF) |
| 136 | Repair Kinetics of Genomic Interstrand DNA Cross-Links: Evidence for DNA Double-Strand Break-Dependent Activation of the Fanconi Anemia/BRCA Pathway | 1.5 | 221 | Citations (PDF) |
| 137 | Liver-Directed Adenoviral Gene Transfer in Murine Succinate Semialdehyde Dehydrogenase Deficiency | 6.0 | 28 | Citations (PDF) |
| 138 | Renal proximal tubular cells acquire resistance to cell death stimuli in mice with hereditary tyrosinemia type 1 | 4.2 | 7 | Citations (PDF) |
| 139 | Myelomonocytic cells are sufficient for therapeutic cell fusion in liver | 22.6 | 421 | Citations (PDF) |
| 140 | Chronic liver disease in murine hereditary tyrosinemia type 1 induces resistance to cell death | 9.6 | 63 | Citations (PDF) |
| 141 | Interstrand crosslink-induced radials form between non-homologous chromosomes, but are absent in sex chromosomes | 1.8 | 32 | Citations (PDF) |
| 142 | Pharmacologic or genetic ablation of maleylacetoacetate isomerase increases levels of toxic tyrosine catabolites in rodents | 3.7 | 31 | Citations (PDF) |
| 143 | Mutational spectrum of the succinate semialdehyde dehydrogenase (ALDH5A1) gene and functional analysis of 27 novel disease-causing mutations in patients with SSADH deficiency | 1.0 | 137 | Citations (PDF) |
| 144 | Murine succinate semialdehyde dehydrogenase deficiency | 4.6 | 49 | Citations (PDF) |
| 145 | Cell fusion is the principal source of bone-marrow-derived hepatocytes | 30.6 | 1,567 | Citations (PDF) |
| 146 | AAV serotype 2 vectors preferentially integrate into active genes in mice | 14.1 | 385 | Citations (PDF) |
| 147 | The Fanconi anaemia/BRCA pathway | 34.5 | 796 | Citations (PDF) |
| 148 | Pancreatic–hepatic switches in vivo | 2.6 | 51 | Citations (PDF) |
| 149 | The Multiple Sulfatase Deficiency Gene Encodes an Essential and Limiting Factor for the Activity of Sulfatases | 23.4 | 341 | Citations (PDF) |
| 150 | Epithelial cancer in Fanconi anemia complementation group D2 (Fancd2) knockout mice | 2.8 | 254 | Citations (PDF) |
| 151 | The origin and liver repopulating capacity of murine oval cells | 5.2 | 405 | Citations (PDF) |
| 152 | Helper-independent and AAV-ITR-independent chromosomal integration of double-stranded linear DNA vectors in mice | 6.0 | 48 | Citations (PDF) |
| 153 | The Role of Bone Marrow Stem Cells in Liver Regeneration | 2.0 | 94 | Citations (PDF) |
| 154 | Reply to “Involvement of oxidative stress in Fanconi's anaemia: from phenotype to FA protein functions” | 34.5 | 0 | Citations (PDF) |
| 155 | In Vivo Correction of Murine Tyrosinemia Type I by DNA-Mediated Transposition | 6.0 | 141 | Citations (PDF) |
| 156 | Attenuation of the formation of DNA-repair foci containing RAD51 in Fanconi anaemia | 2.2 | 84 | Citations (PDF) |
| 157 | BRCA1 interacts directly with the Fanconi anemia protein FANCA | 2.1 | 104 | Citations (PDF) |
| 158 | Therapeutic Intervention in Mice Deficient for Succinate Semialdehyde Dehydrogenase (γ-Hydroxybutyric Aciduria) | 2.3 | 84 | Citations (PDF) |
| 159 | Maleylacetoacetate Isomerase (
MAAI/GSTZ
)-Deficient Mice Reveal a Glutathione-Dependent Nonenzymatic Bypass in Tyrosine Catabolism | 1.5 | 93 | Citations (PDF) |
| 160 | S-phase–specific interaction of the Fanconi anemia protein, FANCD2, with BRCA1 and RAD51Blood, 2002, 100, 2414-2420 | 3.6 | 440 | Citations (PDF) |
| 161 | Gene therapy of Fanconi anemia: preclinical efficacy using lentiviral vectorsBlood, 2002, 100, 2732-2736 | 3.6 | 82 | Citations (PDF) |
| 162 | Kinetics of Liver Repopulation after Bone Marrow Transplantation | 2.8 | 235 | Citations (PDF) |
| 163 | Long-Term Therapy with NTBC and Tyrosine-Restricted Diet in a Murine Model of Hereditary Tyrosinemia Type I | 0.5 | 84 | Citations (PDF) |
| 164 | Mutations in PHF6 are associated with Börjeson–Forssman –Lehmann syndrome | 14.1 | 210 | Citations (PDF) |
| 165 | Sandgren EP, Palmiter RD, Heckel JL, Daugherty CC, Brinster RL, Degen JL. Complete hepatic regeneration after somatic deletion of an albumin–plasminogen activator transgene [Cell 1991;66:245–256] | 6.7 | 9 | Citations (PDF) |
| 166 | Fanconi anemia group A and C double-mutant mice | 0.6 | 63 | Citations (PDF) |
| 167 | In vivo administration of interferon γ does not cause marrow aplasia in mice with a targeted disruption of FANCC | 0.6 | 7 | Citations (PDF) |
| 168 | SV40 large T-antigen disturbs the formation of nuclear DNA-repair foci containing MRE11 | 5.2 | 57 | Citations (PDF) |
| 169 | Transition of Stem Cells to Therapeutically Functional Tissue‐Specific Cells | 2.6 | 6 | Citations (PDF) |
| 170 | The 4N Cell Cycle Delay in Fanconi Anemia Reflects Growth Arrest in Late S Phase | 0.5 | 70 | Citations (PDF) |
| 171 | Liver Repopulation and Correction of Metabolic Liver Disease by Transplanted Adult Mouse Pancreatic Cells | 2.8 | 115 | Citations (PDF) |
| 172 | Pharmacologic rescue of lethal seizures in mice deficient in succinate semialdehyde dehydrogenase | 14.1 | 158 | Citations (PDF) |
| 173 | Positional Cloning of a Novel Fanconi Anemia Gene, FANCD2 | 8.6 | 379 | Citations (PDF) |
| 174 | Interaction of the Fanconi Anemia Proteins and BRCA1 in a Common Pathway | 8.6 | 1,168 | Citations (PDF) |
| 175 | Liver repopulation for the treatment of metabolic diseases | 2.6 | 45 | Citations (PDF) |
| 176 | Functional analysis of patient-derived mutations in the Fanconi anemia gene, FANCG/XRCC9 | 0.6 | 21 | Citations (PDF) |
| 177 | Function of the Fanconi anemia pathway in Fanconi anemia complementation group F and D1 cells | 0.6 | 38 | Citations (PDF) |
| 178 | Preclinical Protocol for in Vivo Selection of Hematopoietic Stem Cells Corrected by Gene Therapy in Fanconi Anemia Group C | 6.0 | 37 | Citations (PDF) |
| 179 | Fanconi anemia and DNA repair | 2.1 | 170 | Citations (PDF) |
| 180 | Mechanistic Inferences from the Crystal Structure of Fumarylacetoacetate Hydrolase with a Bound Phosphorus-based Inhibitor | 1.3 | 59 | Citations (PDF) |
| 181 | The Pathophysiology and Treatment of Hereditary Tyrosinemia Type 1 | 2.0 | 167 | Citations (PDF) |
| 182 | Loss of p27Kip1 enhances the transplantation efficiency of hepatocytes transferred into diseased livers | 6.6 | 46 | Citations (PDF) |
| 183 | Loss of p27Kip1 enhances the transplantation efficiency of hepatocytes transferred into diseased livers | 6.6 | 17 | Citations (PDF) |
| 184 | Purified hematopoietic stem cells can differentiate into hepatocytes in vivo | 22.6 | 2,296 | Citations (PDF) |
| 185 | Phenotypic correction of Fanconi anemia group C knockout mice | 3.6 | 54 | Citations (PDF) |
| 186 | DNA Replication Is Required To Elicit Cellular Responses to Psoralen-Induced DNA Interstrand Cross-Links | 1.5 | 187 | Citations (PDF) |
| 187 | Localization of the Fanconi Anemia Complementation Group D Gene to a 200-kb Region on Chromosome 3p25.3 | 4.0 | 30 | Citations (PDF) |
| 188 | In Vivo Selection of Wild-Type Hematopoietic Stem Cells in a Murine Model of Fanconi AnemiaBlood, 1999, 94, 2151-2158 | 3.6 | 55 | Citations (PDF) |
| 189 | Principles of Therapeutic Liver Repopulation | 2.0 | 84 | Citations (PDF) |
| 190 | In vivo suppressor mutations correct a murine model of hereditary tyrosinemia type I | 5.2 | 50 | Citations (PDF) |
| 191 | Embryonic stem cells can be used to construct hybrid cell lines containing a single, selectable murine chromosome | 1.2 | 2 | Citations (PDF) |
| 192 | Tumor necrosis factor-? and CD95 ligation suppress erythropoiesis in fanconi anemia C gene knockout mice 1999, 179, 79-86 | | 58 | Citations (PDF) |
| 193 | Identification of the mutation in the alkaptonuria mouse model | 1.0 | 50 | Citations (PDF) |
| 194 | The Repopulation Potential of Hepatocyte Populations Differing in Size and Prior Mitotic Expansion | 2.8 | 180 | Citations (PDF) |
| 195 | Gene Structure, Chromosomal Location, and Expression Pattern of Maleylacetoacetate Isomerase | 2.0 | 41 | Citations (PDF) |
| 196 | Ex Vivo
Hepatic Gene Therapy of a Mouse Model of Hereditary Tyrosinemia Type I | 2.3 | 70 | Citations (PDF) |
| 197 | Chemical Cleavage of Heteroduplex DNA to Identify Mutations | 1.4 | 0 | Citations (PDF) |
| 198 | Subtyping Analysis of Fanconi Anemia by Immunoblotting and Retroviral Gene Transfer | 4.3 | 58 | Citations (PDF) |
| 199 | DNA Cross-Linker–Induced G2/M Arrest in Group C Fanconi Anemia Lymphoblasts Reflects Normal Checkpoint Function | 3.6 | 74 | Citations (PDF) |
| 200 | Adenovirus-Mediated Gene Therapy in a Mouse Model of Hereditary Tyrosinemia Type I | 2.3 | 70 | Citations (PDF) |
| 201 | Molecular Biology of Fanconi Anemia: Implications for Diagnosis and TherapyBlood, 1997, 90, 1725-1736 | 3.6 | 195 | Citations (PDF) |
| 202 | Inactivation of the Fanconi Anemia Group C Gene Augments Interferon-γ–Induced Apoptotic Responses in Hematopoietic Cells | 3.6 | 169 | Citations (PDF) |
| 203 | Complementation group assignments in fanconi anemia fibroblast cell lines from North America | 1.3 | 17 | Citations (PDF) |
| 204 | Immortalization of four new fanconi anemia fibroblast cell lines by an improved procedure | 1.3 | 29 | Citations (PDF) |
| 205 | Six novel mutations in the fumarylacetoacetate hydrolase gene of patients with hereditary tyrosinemia type I | 1.0 | 10 | Citations (PDF) |
| 206 | Hepatocytes corrected by gene therapy are selected in vivo in a murine model of hereditary tyrosinaemia type I | 14.1 | 567 | Citations (PDF) |
| 207 | Rapid nonradioactive assay for the detection of the common French Canadian tyrosinemia type I mutation | 1.0 | 10 | Citations (PDF) |
| 208 | Pharmacological correction of neonatal lethal hepatic dysfunction in a murine model of hereditary tyrosinaemia type I | 14.1 | 316 | Citations (PDF) |
| 209 | Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3p | 14.1 | 135 | Citations (PDF) |
| 210 | Spontaneous deletion in the FMR1 gene in a patient with fragile X syndrome and cherubism | 2.1 | 64 | Citations (PDF) |
| 211 | Cloning and Characterization of a Human cDNA (INPPL1) Sharing Homology with Inositol Polyphosphate Phosphatases | 2.0 | 47 | Citations (PDF) |
| 212 | A Single Mutation of the Fumarylacetoacetate Hydrolase Gene in French Canadians with Hereditary Tyrosinemia Type I | 26.5 | 141 | Citations (PDF) |
| 213 | The Ashkenazi Jewish Fanconi anemia mutation: Incidence among patients and carrier frequency in the at-risk population | 1.0 | 41 | Citations (PDF) |
| 214 | Microphthalmia with linear skin defects (MLS) syndrome: Clinical, cytogenetic, and molecular characterization | 0.5 | 100 | Citations (PDF) |
| 215 | Efficiency of Insertion versus Replacement Vector Targeting Varies at Different Chromosomal Loci | 1.5 | 21 | Citations (PDF) |
| 216 | Mutations of the fumarylacetoacetate hydrolase gene in four patients with tyrosinemia, type I | 1.0 | 53 | Citations (PDF) |
| 217 | A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi Jews | 14.1 | 165 | Citations (PDF) |
| 218 | The rapid detection of unknown mutations in nucleic acids | 14.1 | 317 | Citations (PDF) |
| 219 | Loss of fumarylacetoacetate hydrolase is responsible for the neonatal hepatic dysfunction phenotype of lethal albino mice. | 2.8 | 346 | Citations (PDF) |
| 220 | Retroviral-Mediated Gene Transfer of Human Ornithine Transcarbamylase into Primary Hepatocytes of
spf
and
spf-ash
Mice | 2.3 | 58 | Citations (PDF) |
| 221 | The sulfatase gene family: Cross-species PCR cloning using the MOPAC technique | 2.0 | 22 | Citations (PDF) |
| 222 | Nucleotide sequence of a cDNA encoding murine fumarylacetoacetate hydrolase | 0.9 | 14 | Citations (PDF) |
| 223 | Mutations in the Escherichia coli dnaG gene suggest coupling between DNA replication and chromosome partitioning | 2.2 | 54 | Citations (PDF) |
| 224 | Fidelity of targeted recombination in human fibroblasts and murine embryonic stem cells. | 5.2 | 43 | Citations (PDF) |
| 225 | A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome | 30.6 | 1,487 | Citations (PDF) |
| 226 | Characterization of a murine gene expressed from the inactive X chromosome | 30.6 | 556 | Citations (PDF) |
| 227 | Molecular detection and correction of ornithine transcarbamylase deficiency | 5.5 | 15 | Citations (PDF) |
| 228 | Ectopic correction of ornithine transcarbamylase deficiency in sparse fur mice. | 1.3 | 45 | Citations (PDF) |
| 229 | Scanning detection of mutations in human ornithine transcarbamoylase by chemical mismatch cleavage. | 5.2 | 129 | Citations (PDF) |
| 230 | RNA virus expression during and after methylnitrosourea-induced T-cell leukemogenesis in mice | 1.0 | 1 | Citations (PDF) |
| 231 | A comparative study on steroid sulfatase and arylsulfatase C in fibroblast clones from 45,X/47,XXX and 69,XXY | 1.8 | 4 | Citations (PDF) |
| 232 | Cell networks in the mouse liver during partial hepatectomy | 3.0 | 3 | Citations (PDF) |
| 233 | RAAVioli: A comprehensive approach to characterizing AAV vector integrations and rearrangements 0, 34, 201659 | | 1 | Citations (PDF) |
| 234 | A clinically relevant retrograde intraductal injection (RIDI) for lipid nanoparticles-mediated base editing in the pancreas | 2.3 | 0 | Citations (PDF) |