Search Results - "Mapa F"

CellSIUS provides sensitive and specific detection of rare cell populations from complex single-cell RNA-seq data.

Authors: Wegmann R Neri M Schuierer S et al.

Source: Genome biology [Genome Biol] 2019 Jul 17; Vol. 20 (1), pp. 142. Date of Electronic Publication: 2019 Jul 17.

Publication Type: Evaluation Study; 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

LXH254, a Potent and Selective ARAF-Sparing Inhibitor of BRAF and CRAF for the Treatment of MAPK-Driven Tumors.

Authors: Monaco KA Delach S Yuan J et al.

Source: Clinical cancer research : an official journal of the American Association for Cancer Research [Clin Cancer Res] 2021 Apr 01; Vol. 27 (7), pp. 2061-2073. Date of Electronic Publication: 2020 Dec 22.

Publication Type: Journal Article

Journal Info: Publisher: American Association for Cancer Research Country of Publication: United States NLM ID: 9502500 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1557-3265 (Electronic) Linking ISSN: 10780432 NLM ISO Abbreviation: Clin Cancer Res Subsets: MEDLINE

Nannocystin A: an Elongation Factor 1 Inhibitor from Myxobacteria with Differential Anti-Cancer Properties.

Authors: Krastel P Roggo S Schirle M et al.

Source: Angewandte Chemie (International ed. in English) [Angew Chem Int Ed Engl] 2015 Aug 24; Vol. 54 (35), pp. 10149-54. Date of Electronic Publication: 2015 Jul 15.

Publication Type: Journal Article

Journal Info: Publisher: Wiley-VCH Country of Publication: Germany NLM ID: 0370543 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1521-3773 (Electronic) Linking ISSN: 14337851 NLM ISO Abbreviation: Angew Chem Int Ed Engl Subsets: MEDLINE

Single nucleotide polymorphism markers for genetic mapping in Drosophila melanogaster.

Authors: Hoskins RA Phan AC Naeemuddin M et al.

Source: Genome research [Genome Res] 2001 Jun; Vol. 11 (6), pp. 1100-13.

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

Journal Info: Publisher: Cold Spring Harbor Laboratory Press Country of Publication: United States NLM ID: 9518021 Publication Model: Print Cited Medium: Print ISSN: 1088-9051 (Print) Linking ISSN: 10889051 NLM ISO Abbreviation: Genome Res Subsets: MEDLINE

Transferrin receptor mutation analysis in hereditary hemochromatosis patients.

Authors: Tsuchihashi Z Hansen SL Quintana L et al.

Source: Blood cells, molecules & diseases [Blood Cells Mol Dis] 1998 Sep; Vol. 24 (3), pp. 317-21.

Publication Type: Journal Article

Journal Info: Publisher: Academic Press Country of Publication: United States NLM ID: 9509932 Publication Model: Print Cited Medium: Print ISSN: 1079-9796 (Print) Linking ISSN: 10799796 NLM ISO Abbreviation: Blood Cells Mol Dis Subsets: MEDLINE

The hemochromatosis founder mutation in HLA-H disrupts beta2-microglobulin interaction and cell surface expression.

Authors: Feder JN Tsuchihashi Z Irrinki A et al.

Source: The Journal of biological chemistry [J Biol Chem] 1997 May 30; Vol. 272 (22), pp. 14025-8.

Publication Type: Journal Article

Journal Info: Publisher: Elsevier Inc. on behalf of American Society for Biochemistry and Molecular Biology Country of Publication: United States NLM ID: 2985121R Publication Model: Print Cited Medium: Print ISSN: 0021-9258 (Print) Linking ISSN: 00219258 NLM ISO Abbreviation: J Biol Chem Subsets: MEDLINE

A 1.1-Mb transcript map of the hereditary hemochromatosis locus.

Authors: Ruddy DA Kronmal GS Lee VK et al.

Source: Genome research [Genome Res] 1997 May; Vol. 7 (5), pp. 441-56.

Publication Type: Comparative Study; Journal Article

Journal Info: Publisher: Cold Spring Harbor Laboratory Press Country of Publication: United States NLM ID: 9518021 Publication Model: Print Cited Medium: Print ISSN: 1088-9051 (Print) Linking ISSN: 10889051 NLM ISO Abbreviation: Genome Res Subsets: MEDLINE

A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis.

Authors: Feder JN Gnirke A Thomas W et al.

Source: Nature genetics [Nat Genet] 1996 Aug; Vol. 13 (4), pp. 399-408.

Publication Type: Comparative Study; Journal Article

Journal Info: Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print Cited Medium: Print ISSN: 1061-4036 (Print) Linking ISSN: 10614036 NLM ISO Abbreviation: Nat Genet Subsets: MEDLINE

One hundred and one new simple sequence repeat-based markers for the canine genome.

Authors: Ostrander EA Mapa FA Yee M et al.

Source: Mammalian genome : official journal of the International Mammalian Genome Society [Mamm Genome] 1995 Mar; Vol. 6 (3), pp. 192-5.

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

Journal Info: Publisher: Springer-Verlag Country of Publication: United States NLM ID: 9100916 Publication Model: Print Cited Medium: Print ISSN: 0938-8990 (Print) Linking ISSN: 09388990 NLM ISO Abbreviation: Mamm Genome Subsets: MEDLINE