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Journal of General Internal Medicine, ISSN 0884-8734, 8/2018, Volume 33, Issue 8, pp. 1218 - 1220
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1007/s11606-018-4455-1 
choosing wisely | Medicine & Public Health | Pharmacoeconomics | physician sentiment | Internal Medicine | provider communication | hidden curriculum | MEDICINE, GENERAL & INTERNAL | HEALTH CARE SCIENCES & SERVICES | OUTCOMES | Medical colleges | Acetaminophen | Analysis | Cardiovascular agents | Concise Research Reports
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Journal of General Internal Medicine, ISSN 0884-8734, 6/2018, Volume 33, Issue 6, pp. 809 - 811
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1007/s11606-018-4395-9 (2) 0000... 
Medicine & Public Health | outreach | response | pragmatic trial | electronic | Internal Medicine | asthma | telephone | beta-agonist | communication technology | MEDICINE, GENERAL & INTERNAL | HEALTH CARE SCIENCES & SERVICES | Health maintenance organizations | Behavioral health care | Children | Technology | Health aspects | Asthma | Concise Research Reports
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Journal of General Internal Medicine, ISSN 0884-8734, 4/2018, Volume 33, Issue 4, pp. 404 - 405
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1007/s11606-017-4300-y 
Medicine & Public Health | Internal Medicine | MEDICINE, GENERAL & INTERNAL | EXPECTATIONS | PREDICTORS | MENTAL-DISORDERS | HEALTH CARE SCIENCES & SERVICES | Clinics | Health care | Concise Research Reports
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The Journal of Infectious Diseases, ISSN 0022-1899, 4/2002, Volume 185, Issue 8, pp. 1197 - 1202
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Journal of Clinical Investigation, ISSN 0021-9738, 08/2018, Volume 128, Issue 8, pp. 3312 - 3318
For gene therapy of gain-of-function autosomal dominant diseases, either correcting or deleting the disease allele is potentially curative. To test whether... 
MEDICINE, RESEARCH & EXPERIMENTAL | CXCR4 ANTAGONIST PLERIXAFOR | MYELOKATHEXIS | MOBILIZATION | MICE | STEM-CELL TRANSPLANTATION | IMMUNODEFICIENCY | HEMATOPOIETIC STEM | Immunologic Deficiency Syndromes - pathology | Immunologic Deficiency Syndromes - therapy | Warts - therapy | Leukopenia - genetics | Leukopenia - pathology | Leukopenia - therapy | Warts - metabolism | Haploinsufficiency | Receptors, CXCR4 - metabolism | Transplantation Chimera - genetics | Transplantation Chimera - metabolism | Leukopenia - metabolism | Warts - pathology | Allografts | Animals | Mice, Mutant Strains | Bone Marrow Transplantation | Immunologic Deficiency Syndromes - genetics | Immunologic Deficiency Syndromes - metabolism | Receptors, CXCR4 - genetics | Mice | Warts - genetics | Disease Models, Animal | Care and treatment | Physiological aspects | Bone marrow | Immunological deficiency syndromes | Genetic aspects | Leucopenia | Transplantation | Research | Properties | Health aspects | Chemokine receptors | Risk factors | Competition | Animal models | Disease | Syngeneic grafts | Bone marrow transplantation | Hypogammaglobulinemia | Retention | Experiments | Hematopoietic stem cells | Genotype & phenotype | Clonal deletion | Rodents | Neutropenia | Leukopenia | Neutrophils | Immunodeficiency | Patients | CXCR4 protein | Hemopoiesis | Warts | Alleles | Stem cells | Chimerism | Mutation | Gene therapy | Chemokines
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Journal of Clinical Investigation, ISSN 0021-9738, 05/2018, Volume 128, Issue 5, pp. 2042 - 2047
Mice homozygous for the Tyr208Asn amino acid substitution in the carboxy terminus of Src homology region 2 (SH2) domain-containing phosphatase 1 (SHP-1)... 
MEDICINE, RESEARCH & EXPERIMENTAL | APOPTOSIS | GENE | TAK1 | AUTOIMMUNITY | INNATE | ACTIVATED PROTEIN-KINASES | STRESS | Inflammation - pathology | Protein Tyrosine Phosphatase, Non-Receptor Type 6 - immunology | Neutrophil Infiltration | Sweet Syndrome - genetics | Signal Transduction - immunology | MAP Kinase Kinase Kinase 5 - metabolism | Disease Models, Animal | Neutrophils - pathology | Sweet Syndrome - immunology | MAP Kinase Kinase Kinase 5 - genetics | Neutrophils - enzymology | MAP Kinase Kinase Kinases - genetics | Neutrophils - immunology | Sweet Syndrome - pathology | Inflammation - immunology | MAP Kinase Kinase Kinases - metabolism | Signal Transduction - genetics | Protein Tyrosine Phosphatase, Non-Receptor Type 6 - genetics | MAP Kinase Kinase Kinases - immunology | Mice, Knockout | Animals | Sweet Syndrome - enzymology | Inflammation - genetics | Mice | Inflammation - enzymology | MAP Kinase Kinase Kinase 5 - immunology | Neutrophils | Physiological aspects | Development and progression | Models | Inflammation | Skin | Autoimmune diseases | Dermatitis | Health aspects | Mitogen-activated protein kinases | Splenomegaly | SHP-1 protein | TAK1 protein | MAP kinase | Homology | Leukocytes (neutrophilic) | Interleukin 1 receptors | Kinases | Amino acid substitution | Clonal deletion | Interleukin 1 | Skin diseases | Syk protein | Mutation | Apoptosis
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Indian dermatology online journal, ISSN 2229-5178, 09/2018, Volume 9, Issue 5, pp. 338 - 340
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Indian dermatology online journal, ISSN 2229-5178, 07/2019, Volume 10, Issue 4, pp. 471 - 472
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Indian dermatology online journal, ISSN 2229-5178, 05/2019, Volume 10, Issue 3, pp. 330 - 331
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