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Mashup Score: 0Wolters Kluwer Health - 10 month(s) ago
JavaScript Error JavaScript has been disabled on your browser. You must enable it to continue. Here’s how to enable JavaScript in the following browsers: Internet Explorer From the Tools menu, select Options Click the Content tab Select Enable JavaScript Firefox From the Tools…
Source: lww.comCategories: Hem/Oncs, Latest HeadlinesTweet
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Mashup Score: 0CRISPR/Cas9-mediated Cxcr4 disease allele inactivation for gene therapy in a mouse model of WHIM syndrome - 10 month(s) ago
Key Points. A 2-step gene therapy protocol of autologous HSPC transplantation for WHIM syndrome by CRISPR/Cas9-mediated disease allele inactivation.WHIM disease
Source: American Society of HematologyCategories: Hem/Oncs, Latest HeadlinesTweet-
https://t.co/Qo7bVCrJcX
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Mashup Score: 1The clinical picture of ERCC6L2 disease: from bone marrow failure to acute leukemia - 11 month(s) ago
Key Points. ERCC6L2 disease causes BMF that requires timely stem cell transplantation before progressing to a high-risk myeloid malignancy.Frequent somatic TP53
Source: American Society of HematologyCategories: Hem/Oncs, Latest HeadlinesTweet-
The clinical picture of ERCC6L2 disease: from bone marrow failure to acute leukemia | Blood | American Society of Hematology https://t.co/sLXLmaYYGY
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Mashup Score: 0Selective homing of CAR-CIK cells to the bone marrow niche enhances control of the acute myeloid leukemia burden - 12 month(s) ago
Key Points. CAR T-cell therapy in AML is hampered by the poor accumulation of effector cells in the BM niche in which leukemic stem cells are nested.Engineering
Source: American Society of HematologyCategories: Hem/Oncs, Latest HeadlinesTweet-
Selective homing of CAR-CIK cells to the bone marrow niche enhances control of the acute myeloid leukemia burden | Blood | American Society of Hematology https://t.co/aXJZqZN2UG
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Mashup Score: 2Somatic genetic rescue in Mendelian haematopoietic diseases - Nature Reviews Genetics - 1 year(s) ago
Somatic genetic rescue (SGR) occurs when an acquired somatic mutation counteracts the effects of a germline mutation at a cellular level. The increasing number of SGR events reported for Mendelian haematopoietic diseases have important diagnostic, therapeutic and clinical consequences.
Source: NatureCategories: Hem/Oncs, Latest HeadlinesTweet-
Interested in hematopoiesis and need something extremely interesting to read? https://t.co/geaz21l36x
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Mashup Score: 0Idiopathic bone marrow dysplasia of unknown significance (IDUS): definition, pathogenesis, follow up, and prognosis - 1 year(s) ago
Minimal diagnostic criteria for myelodysplastic syndromes (MDS) include constant cytopenia recorded for at least 6 months, dysplasia, and exclusion of other causes of cytopenia and dysplasia. However, there are patients with dysplastic bone marrow features …
Source: PubMed Central (PMC)Categories: Hem/Oncs, Latest HeadlinesTweet-
If “idiopathic dysplasia of uncertain significance” is a thing, how about “clonal dysplasia of uncertain significance” in patients with clones, dysplasia, but no cytopenias? can you have MDS with no cytopenia? 🤯#hematology @DavidSteensma https://t.co/qXA7ePcYrW
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Mashup Score: 3Please wait whilst we redirect you - 1 year(s) ago
About ScienceDirectRemote accessShopping cartAdvertiseContact and supportTerms and conditionsPrivacy policyWe use cookies to help provide and enhance our service and tailor content and ads. By continuing you agree to the use of cookies.Copyright © 2023 Elsevier B.V. or its licensors or contributors. ScienceDirect® is a registered trademark of Elsevier B.V.ScienceDirect® is a registered trademark…
Source: www.sciencedirect.comCategories: Hem/Oncs, Latest HeadlinesTweet-
RT @pillai_vinodh: Excited to share our work on using LEF1 to identify Burkitt lymphoma with 11q aberrations https://t.co/nerhkT5dJm
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Mashup Score: 2
Key Points. Using whole genome sequencing and RNA-seq, we characterized the genomic landscape of 295 DS-ALL cases and identified 15 distinct subtypes.DS-ALL exh
Source: American Society of HematologyCategories: Hem/Oncs, Latest HeadlinesTweet-
RT @BloodJournal: Genomic landscape of Down syndrome-associated acute lymphoblastic leukemia https://t.co/nzVwAyJLtg
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Mashup Score: 7Transcobalamin II deficiency at birth - 1 year(s) ago
Transcobalamin II deficiency (# MIM 275350) is a rare, recessively inherited disorder of cobalamin transport that leads to intracellular cobalamin dep…
Source: www.sciencedirect.comCategories: Hem/Oncs, Latest HeadlinesTweet-
Large myeloid precursors with vacuolization in the bone marrow of a patient transcobalamin II deficiency (TCN2 gene mutation). #hemepath Image from: https://t.co/5Z7r2rlfOC https://t.co/wp3tYj3Suj
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Mashup Score: 8Please wait whilst we redirect you - 1 year(s) ago
About ScienceDirectRemote accessShopping cartAdvertiseContact and supportTerms and conditionsPrivacy policyWe use cookies to help provide and enhance our service and tailor content and ads. By continuing you agree to the use of cookies.Copyright © 2023 Elsevier B.V. or its licensors or contributors. ScienceDirect® is a registered trademark of Elsevier B.V.ScienceDirect® is a registered trademark…
Source: www.sciencedirect.comCategories: Hem/Oncs, Latest HeadlinesTweet-
Review on IgG4 related lymphadenopathy #hemepath https://t.co/BgyIcftzJS
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Spectrum of Liver Pathology in Dyskeratosis Congenita : The American Journal of Surgical Pathology https://t.co/qy0w0xD1gp