Linch DC - Search Results

1

In trans early mosaic mutational escape and novel phenotypic features of germline SAMD9 mutation.

Hockings C, Gohil S, Dowse R, Hoade Y, Mansour MR, Gale RE, Linch DC, Rao A, Payne EM. Hockings C, et al. Among authors: linch dc. Br J Haematol. 2020 Feb;188(4):e53-e57. doi: 10.1111/bjh.16322. Epub 2020 Jan 3. Br J Haematol. 2020. PMID: 31900929 Free article. No abstract available.

2

Therapy for isocitrate dehydrogenase 2 (IDH2)^R172 -mutant acute myeloid leukaemia.

Linch DC, Hills RK, Burnett AK, Russell N, Gale RE. Linch DC, et al. Br J Haematol. 2022 Mar;196(6):1348-1352. doi: 10.1111/bjh.17981. Epub 2021 Dec 6. Br J Haematol. 2022. PMID: 34870324

3

Long-term follow-up of granulocyte colony-stimulating factor receptor mutations in patients with severe congenital neutropenia: implications for leukaemogenesis and therapy.

Ancliff PJ, Gale RE, Liesner R, Hann I, Linch DC. Ancliff PJ, et al. Among authors: linch dc. Br J Haematol. 2003 Feb;120(4):685-90. doi: 10.1046/j.1365-2141.2003.04160.x. Br J Haematol. 2003. PMID: 12588357 Free article.

4

Neutrophil elastase mutations in congenital neutropenia.

Ancliff PJ, Gale RE, Linch DC. Ancliff PJ, et al. Among authors: linch dc. Hematology. 2003 Jun;8(3):165-71. doi: 10.1080/1024533031000107497. Hematology. 2003. PMID: 12745650 Free article. Review.

5

Flt3 mutations and leukaemia.

Kottaridis PD, Gale RE, Linch DC. Kottaridis PD, et al. Among authors: linch dc. Br J Haematol. 2003 Aug;122(4):523-38. doi: 10.1046/j.1365-2141.2003.04500.x. Br J Haematol. 2003. PMID: 12899708 Free article. Review. No abstract available.

6

Acute myeloid leukaemia blast cells with a tyrosine kinase domain mutation of FLT3 are less sensitive to lestaurtinib than those with a FLT3 internal tandem duplication.

Mead AJ, Gale RE, Kottaridis PD, Matsuda S, Khwaja A, Linch DC. Mead AJ, et al. Among authors: linch dc. Br J Haematol. 2008 May;141(4):454-60. doi: 10.1111/j.1365-2141.2008.07025.x. Epub 2008 Mar 12. Br J Haematol. 2008. PMID: 18341639 Free article.

7

Most acute myeloid leukaemia patients with intermediate mutant FLT3/ITD levels do not have detectable bi-allelic disease, indicating that heterozygous disease alone is associated with an adverse outcome.

Green C, Linch DC, Gale RE. Green C, et al. Among authors: linch dc. Br J Haematol. 2008 Jul;142(3):423-6. doi: 10.1111/j.1365-2141.2008.07196.x. Epub 2008 Jun 3. Br J Haematol. 2008. PMID: 18537976 Free article.

8

Homozygous HAX1 mutations in severe congenital neutropenia patients with sporadic disease: a novel mutation in two unrelated British kindreds.

Smith BN, Ancliff PJ, Pizzey A, Khwaja A, Linch DC, Gale RE. Smith BN, et al. Among authors: linch dc. Br J Haematol. 2009 Mar;144(5):762-70. doi: 10.1111/j.1365-2141.2008.07493.x. Epub 2008 Nov 22. Br J Haematol. 2009. PMID: 19036076 Free article.

9

The production of JAK2 wild-type platelets is not downregulated in patients with JAK2 V617F mutant-positive essential thrombocythaemia.

Lambert JR, Gale RE, Linch DC. Lambert JR, et al. Among authors: linch dc. Br J Haematol. 2009 Apr;145(1):128-30. doi: 10.1111/j.1365-2141.2009.07597.x. Epub 2009 Jan 12. Br J Haematol. 2009. PMID: 19222478 Free article.

10

GATA2 mutations in sporadic and familial acute myeloid leukaemia patients with CEBPA mutations.

Green CL, Tawana K, Hills RK, Bödör C, Fitzgibbon J, Inglott S, Ancliff P, Burnett AK, Linch DC, Gale RE. Green CL, et al. Among authors: linch dc. Br J Haematol. 2013 Jun;161(5):701-705. doi: 10.1111/bjh.12317. Epub 2013 Apr 5. Br J Haematol. 2013. PMID: 23560626 Free article.

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