Search Results

Cellular and molecular architecture of hematopoietic stem cells and progenitors in genetic models of bone marrow failure.

• Authors : Heidemann S; Genetics & Genome Biology Program and.; Marrow Failure and Myelodysplasia (Pre-leukemia) Program, Division of Hematology/Oncology, Department of Pediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada.

Subjects: Models, Genetic*; Bone Marrow Failure Disorders/Bone Marrow Failure Disorders/Bone Marrow Failure Disorders/*pathology ; Hematopoietic Stem Cells/Hematopoietic Stem Cells/Hematopoietic Stem Cells/*pathology

• Source: JCI insight [JCI Insight] 2020 Feb 27; Vol. 5 (4). Date of Electronic Publication: 2020 Feb 27.Publisher: American Society for Clinical Investigation Country of Publication: United States NLM ID: 101676073 Publication Model:

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Mutations in 2 distinct genetic pathways result in cerebral cavernous malformations in mice.

• Authors : Chan AC; Molecular Medicine Program, University of Utah, Salt Lake City, Utah, USA.; Drakos SG

Subjects: Models, Genetic* ; Mutation*; Hemangioma, Cavernous, Central Nervous System/Hemangioma, Cavernous, Central Nervous System/Hemangioma, Cavernous, Central Nervous System/*genetics

• Source: The Journal of clinical investigation [J Clin Invest] 2011 May; Vol. 121 (5), pp. 1871-81. Date of Electronic Publication: 2011 Apr 01.Publisher: American Society for Clinical Investigation Country of Publication: United States NLM ID: 7802877 Publication Model:

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Can you hear me now? A genetic model of otitis media with effusion.

• Authors : Lazaridis E; Department of Otorhinolaryngology, Head and Neck Surgery, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA. ; Saunders JC

Subjects: Models, Genetic*; Ear, Middle/Ear, Middle/Ear, Middle/*abnormalities ; Hearing Loss, Sensorineural/Hearing Loss, Sensorineural/Hearing Loss, Sensorineural/*genetics

• Source: The Journal of clinical investigation [J Clin Invest] 2008 Feb; Vol. 118 (2), pp. 471-4.Publisher: American Society for Clinical Investigation Country of Publication: United States NLM ID: 7802877 Publication Model:

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Mapping quantitative trait loci in humans: achievements and limitations.

• Authors : Majumder PP; Human Genetics Unit, Indian Statistical Institute, Kolkata, India. ; Ghosh S

Subjects: Genome, Human* ; Linkage Disequilibrium* ; Models, Genetic*

• Source: The Journal of clinical investigation [J Clin Invest] 2005 Jun; Vol. 115 (6), pp. 1419-24.Publisher: American Society for Clinical Investigation Country of Publication: United States NLM ID: 7802877 Publication Model:

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Factors affecting statistical power in the detection of genetic association.

• Authors : Gordon D; Laboratory of Statistical Genetics, Rockefeller University, New York, New York 10021, USA. ; Finch SJ

Subjects: Linkage Disequilibrium* ; Lod Score* ; Models, Genetic*

• Source: The Journal of clinical investigation [J Clin Invest] 2005 Jun; Vol. 115 (6), pp. 1408-18.Publisher: American Society for Clinical Investigation Country of Publication: United States NLM ID: 7802877 Publication Model:

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Genetic models: clues for understanding the pathogenesis of idiopathic nephrotic syndrome.

• Authors : Antignac C; Department of Genetics and Institut National de la Santé et de la Recherche Médicale U423, Tour Lavoisier 6 étage, Hôpital Necker, 149 rue de Sèvres, 75015 Paris, France.

Subjects: Models, Genetic*; Nephrotic Syndrome/Nephrotic Syndrome/Nephrotic Syndrome/*etiology ; Nephrotic Syndrome/Nephrotic Syndrome/Nephrotic Syndrome/*genetics

• Source: The Journal of clinical investigation [J Clin Invest] 2002 Feb; Vol. 109 (4), pp. 447-9.Publisher: American Society for Clinical Investigation Country of Publication: United States NLM ID: 7802877 Publication Model:

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The two-domain hypothesis in Beckwith-Wiedemann syndrome.

• Authors : Feinberg AP

Subjects: Models, Genetic*; Beckwith-Wiedemann Syndrome/Beckwith-Wiedemann Syndrome/Beckwith-Wiedemann Syndrome/*genetics ; Enhancer Elements, Genetic/Enhancer Elements, Genetic/Enhancer Elements, Genetic/*genetics

• Source: The Journal of clinical investigation [J Clin Invest] 2000 Sep; Vol. 106 (6), pp. 739-40.Publisher: American Society for Clinical Investigation Country of Publication: United States NLM ID: 7802877 Publication Model:

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A genetic model of substrate deprivation therapy for a glycosphingolipid storage disorder.

• Authors : Liu Y; Genetics of Development and Disease Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.; Wada R

Subjects: Models, Genetic*; Glycosphingolipids/Glycosphingolipids/Glycosphingolipids/*metabolism ; N-Acetylgalactosaminyltransferases/N-Acetylgalactosaminyltransferases/N-Acetylgalactosaminyltransferases/*physiology

• Source: The Journal of clinical investigation [J Clin Invest] 1999 Feb; Vol. 103 (4), pp. 497-505.Publisher: American Society for Clinical Investigation Country of Publication: United States NLM ID: 7802877 Publication Model:

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Convergent generation of atypical prions in knockin mouse models of genetic prion disease

• Authors : Mehra, Surabhi; Bourkas, Matthew E.C.; Kaczmarczyk, Lech

• Source: Journal of Clinical Investigation. August 1, 2024, Vol. 134 Issue 15

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Transcriptional and cytopathological hallmarks of FSHD in chronic DUX4-expressing mice

• Authors : Bosnakovski, Darko; Shams, Ahmed S.; Yuan, Ce

• Source: Journal of Clinical Investigation. May, 2020, Vol. 130 Issue 5, p2465, 13 p.

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