Search Results - "Fu MP"

A Germline Heterozygous Dominant Negative IKZF2 Variant Causing Syndromic Primary Immune Regulatory Disorder and ICHAD.

Authors: Lu HY Vaseghi-Shanjani M Lam AJ et al.

Corporate Authors: Lu HY Vaseghi-Shanjani M Lam AJ et al.

Source: Journal of clinical immunology [J Clin Immunol] 2025 Apr 28; Vol. 45 (1), pp. 89. Date of Electronic Publication: 2025 Apr 28.

Publication Type: Journal Article; Case Reports

Journal Info: Publisher: Springer Country of Publication: Netherlands NLM ID: 8102137 Publication Model: Electronic Cited Medium: Internet ISSN: 1573-2592 (Electronic) Linking ISSN: 02719142 NLM ISO Abbreviation: J Clin Immunol Subsets: MEDLINE

RAMEN: Dissecting individual, additive and interactive gene-environment contributions to DNA methylome variability in cord blood.

Authors: Navarro-Delgado EI Czamara D Edwards K et al.

Source: Genome biology [Genome Biol] 2025 Dec 10; Vol. 26 (1), pp. 421. Date of Electronic Publication: 2025 Dec 10.

Publication Type: Journal Article

Journal Info: Publisher: BioMed Central Ltd Country of Publication: England NLM ID: 100960660 Publication Model: Electronic Cited Medium: Internet ISSN: 1474-760X (Electronic) Linking ISSN: 14747596 NLM ISO Abbreviation: Genome Biol Subsets: MEDLINE

ASXL1 deficiency causes epigenetic dysfunction, combined immunodeficiency, and EBV-associated lymphoma.

Authors: Fu MP Sharma M Yousefi P et al.

Source: The Journal of experimental medicine [J Exp Med] 2025 Oct 06; Vol. 222 (10). Date of Electronic Publication: 2025 Jul 31.

Publication Type: Journal Article; Case Reports

Journal Info: Publisher: Rockefeller University Press Country of Publication: United States NLM ID: 2985109R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1540-9538 (Electronic) Linking ISSN: 00221007 NLM ISO Abbreviation: J Exp Med Subsets: MEDLINE

Examining cellular heterogeneity in human DNA methylation studies: Overview and recommendations.

Authors: Fu MP Merrill SM Korthauer K et al.

Source: STAR protocols [STAR Protoc] 2025 Mar 21; Vol. 6 (1), pp. 103638. Date of Electronic Publication: 2025 Feb 12.

Publication Type: Journal Article; Review

Journal Info: Publisher: Cell Press Country of Publication: United States NLM ID: 101769501 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2666-1667 (Electronic) Linking ISSN: 26661667 NLM ISO Abbreviation: STAR Protoc Subsets: MEDLINE

Rare diseases of epigenetic origin: Challenges and opportunities.

Authors: Fu MP Merrill SM Sharma M et al.

Source: Frontiers in genetics [Front Genet] 2023 Feb 06; Vol. 14, pp. 1113086. Date of Electronic Publication: 2023 Feb 06 (Print Publication: 2023).

Publication Type: Journal Article; Review

Journal Info: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101560621 Publication Model: eCollection Cited Medium: Print ISSN: 1664-8021 (Print) Linking ISSN: 16648021 NLM ISO Abbreviation: Front Genet Subsets: PubMed not MEDLINE

Associations of peripheral blood DNA methylation and estimated monocyte proportion differences during infancy with toddler attachment style.

Authors: Merrill SM Gladish N Fu MP et al.

Source: Attachment & human development [Attach Hum Dev] 2023 Feb; Vol. 25 (1), pp. 132-161. Date of Electronic Publication: 2021 Jul 01.

Publication Type: Journal Article

Journal Info: Publisher: Informa Healthcare Country of Publication: England NLM ID: 100901315 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1469-2988 (Electronic) Linking ISSN: 14616734 NLM ISO Abbreviation: Attach Hum Dev Subsets: MEDLINE

Prognostic role of diuretic failure in determining mortality for patients hospitalized with acute decompensated heart failure.

Authors: Mumtaz S Sharma M Fu MP et al.

Source: Heart and vessels [Heart Vessels] 2022 Aug; Vol. 37 (8), pp. 1373-1379. Date of Electronic Publication: 2022 Feb 18.

Publication Type: Journal Article; Multicenter Study

Journal Info: Publisher: Springer Verlag Country of Publication: Japan NLM ID: 8511258 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1615-2573 (Electronic) Linking ISSN: 09108327 NLM ISO Abbreviation: Heart Vessels Subsets: MEDLINE

Selection for Anti-transferrin Receptor Bispecific T-cell Engager in Different Molecular Formats.

Authors: Fu MP Guo ZL Tang HL et al.

Source: Current medical science [Curr Med Sci] 2020 Feb; Vol. 40 (1), pp. 28-34. Date of Electronic Publication: 2020 Mar 13.

Publication Type: Journal Article

Journal Info: Publisher: Huazhong University of Science and Technology Country of Publication: China NLM ID: 101729993 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2523-899X (Electronic) Linking ISSN: 2523899X NLM ISO Abbreviation: Curr Med Sci Subsets: MEDLINE

Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease.

Authors: Sharma M Leung D Momenilandi M et al.

Source: The Journal of experimental medicine [J Exp Med] 2023 May 01; Vol. 220 (5). Date of Electronic Publication: 2023 Mar 08.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Intramural

Journal Info: Publisher: Rockefeller University Press Country of Publication: United States NLM ID: 2985109R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1540-9538 (Electronic) Linking ISSN: 00221007 NLM ISO Abbreviation: J Exp Med Subsets: MEDLINE

Human complete NFAT1 deficiency causes a triad of joint contractures, osteochondromas, and B-cell malignancy.

Authors: Sharma M Fu MP Lu HY et al.

Source: Blood [Blood] 2022 Oct 27; Vol. 140 (17), pp. 1858-1874.

Publication Type: Journal Article

Journal Info: Publisher: Elsevier Country of Publication: United States NLM ID: 7603509 Publication Model: Print Cited Medium: Internet ISSN: 1528-0020 (Electronic) Linking ISSN: 00064971 NLM ISO Abbreviation: Blood Subsets: MEDLINE