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See also: FERMT3 fermitin family member 3 in the Gene database

fermt3 in Homo sapiensMus musculusRattus norvegicusAll 207 Gene records

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Items: 1 to 20 of 34


Use of Targeted High-Throughput Sequencing for Genetic Classification of Patients with Bleeding Diathesis and Suspected Platelet Disorder.

Andres O, König EM, Althaus K, Bakchoul T, Bugert P, Eber S, Knöfler R, Kunstmann E, Manukjan G, Meyer O, Strauß G, Streif W, Thiele T, Wiegering V, Klopocki E, Schulze H; THROMKIDplus Study Group of the Society of Paediatric Oncology Haematology (Gesellschaft für Pädiatrische Onkologie und Hämatologie, GPOH) and the Society of Thrombosis Haemostasis Research (Gesellschaft für Thrombose- und Hämostaseforschung, GTH) .

TH Open. 2018 Dec 30;2(4):e445-e454. doi: 10.1055/s-0038-1676813. eCollection 2018 Oct.


A Novel Nonsense Mutation in FERMT3 Causes LAD-III in a Pakistani Family.

Shahid S, Zaidi S, Ahmed S, Siddiqui S, Abid A, Malik S, Shamsi T.

Front Genet. 2019 Apr 24;10:360. doi: 10.3389/fgene.2019.00360. eCollection 2019.


Multiomics analysis profile acute liver injury module clusters to compare the therapeutic efficacy of bifendate and muaddil sapra.

Talifu A, Saimaiti R, Maitinuer Y, Liu G, Abudureyimu M, Xin X.

Sci Rep. 2019 Mar 13;9(1):4335. doi: 10.1038/s41598-019-40356-5.


Hepatitis B virus X protein related lncRNA WEE2-AS1 promotes hepatocellular carcinoma proliferation and invasion.

Hu Z, Huang P, Yan Y, Zhou Z, Wang J, Wu G.

Biochem Biophys Res Commun. 2019 Jan 1;508(1):79-86. doi: 10.1016/j.bbrc.2018.11.091. Epub 2018 Nov 22.


Leucocyte adhesion deficiency-A multicentre national experience.

Wolach B, Gavrieli R, Wolach O, Stauber T, Abuzaitoun O, Kuperman A, Amir Y, Stepensky P, Somech R, Etzioni A.

Eur J Clin Invest. 2019 Feb;49(2):e13047. doi: 10.1111/eci.13047. Epub 2019 Jan 4.


Network-Based Predictors of Progression in Head and Neck Squamous Cell Carcinoma.

Sanati N, Iancu OD, Wu G, Jacobs JE, McWeeney SK.

Front Genet. 2018 May 29;9:183. doi: 10.3389/fgene.2018.00183. eCollection 2018.


Identification of potential crucial genes and construction of microRNA-mRNA negative regulatory networks in osteosarcoma.

Pan Y, Lu L, Chen J, Zhong Y, Dai Z.

Hereditas. 2018 May 9;155:21. doi: 10.1186/s41065-018-0061-9. eCollection 2018.


A proteomic approach reveals the variation in human platelet protein composition after storage at different temperatures.

Wang S, Jiang T, Fan Y, Zhao S.

Platelets. 2019;30(3):403-412. doi: 10.1080/09537104.2018.1453060. Epub 2018 Mar 29.


iTRAQ-Based Proteomic Analysis Reveals Protein Profile in Plasma from Children with Autism.

Shen L, Zhang K, Feng C, Chen Y, Li S, Iqbal J, Liao L, Zhao Y, Zhai J.

Proteomics Clin Appl. 2018 May;12(3):e1700085. doi: 10.1002/prca.201700085. Epub 2018 Jan 18.


Variable impairment of platelet functions in patients with severe, genetically linked immune deficiencies.

Nagy M, Mastenbroek TG, Mattheij NJA, de Witt S, Clemetson KJ, Kirschner J, Schulz AS, Vraetz T, Speckmann C, Braun A, Cosemans JMEM, Zieger B, Heemskerk JWM.

Haematologica. 2018 Mar;103(3):540-549. doi: 10.3324/haematol.2017.176974. Epub 2017 Dec 14.


FERMT3 contributes to glioblastoma cell proliferation and chemoresistance to temozolomide through integrin mediated Wnt signaling.

Lu C, Cui C, Liu B, Zou S, Song H, Tian H, Zhao J, Li Y.

Neurosci Lett. 2017 Sep 14;657:77-83. doi: 10.1016/j.neulet.2017.07.057. Epub 2017 Aug 1.


Hematopoietic stem cell transplantation corrects osteopetrosis in a child carrying a novel homozygous mutation in the FERMT3 gene.

Palagano E, Slatter MA, Uva P, Menale C, Villa A, Abinun M, Sobacchi C.

Bone. 2017 Apr;97:126-129. doi: 10.1016/j.bone.2017.01.012. Epub 2017 Jan 14.


The kindlin family: functions, signaling properties and implications for human disease.

Rognoni E, Ruppert R, Fässler R.

J Cell Sci. 2016 Jan 1;129(1):17-27. doi: 10.1242/jcs.161190. Review.


Adaptive immune defects in a patient with leukocyte adhesion deficiency type III with a novel mutation in FERMT3.

Suratannon N, Yeetong P, Srichomthong C, Amarinthnukrowh P, Chatchatee P, Sosothikul D, van Hagen PM, van der Burg M, Wentink M, Driessen GJ, Suphapeetiporn K, Shotelersuk V.

Pediatr Allergy Immunol. 2016 Mar;27(2):214-7. doi: 10.1111/pai.12485. Epub 2015 Oct 22. No abstract available.


Kindlin 3 (FERMT3) is associated with unstable atherosclerotic plaques, anti-inflammatory type II macrophages and upregulation of beta-2 integrins in all major arterial beds.

Oksala N, Pärssinen J, Seppälä I, Klopp N, Illig T, Laaksonen R, Levula M, Raitoharju E, Kholova I, Sioris T, Kähönen M, Lehtimäki T, Hytönen VP.

Atherosclerosis. 2015 Sep;242(1):145-54. doi: 10.1016/j.atherosclerosis.2015.06.058. Epub 2015 Jul 13.


A new mutation in the KINDLIN-3 gene ablates integrin-dependent leukocyte, platelet, and osteoclast function in a patient with leukocyte adhesion deficiency-III.

Crazzolara R, Maurer K, Schulze H, Zieger B, Zustin J, Schulz AS.

Pediatr Blood Cancer. 2015 Sep;62(9):1677-9. doi: 10.1002/pbc.25537. Epub 2015 Apr 8.


Diverse functions of kindlin/fermitin proteins during embryonic development in Xenopus laevis.

Rozario T, Mead PE, DeSimone DW.

Mech Dev. 2014 Aug;133:203-17. doi: 10.1016/j.mod.2014.07.004. Epub 2014 Aug 28.


Differences in binding to the ILK complex determines kindlin isoform adhesion localization and integrin activation.

Huet-Calderwood C, Brahme NN, Kumar N, Stiegler AL, Raghavan S, Boggon TJ, Calderwood DA.

J Cell Sci. 2014 Oct 1;127(Pt 19):4308-21. doi: 10.1242/jcs.155879. Epub 2014 Aug 1.


Skeletal dysplasias with increased bone density: evolution of molecular pathogenesis in the last century.

Aggarwal S.

Gene. 2013 Oct 1;528(1):41-5. doi: 10.1016/j.gene.2013.04.069. Epub 2013 May 5. Review.


Expression and function of FERMT genes in colon carcinoma cells.

Kiriyama K, Hirohashi Y, Torigoe T, Kubo T, Tamura Y, Kanaseki T, Takahashi A, Nakazawa E, Saka E, Ragnarsson C, Nakatsugawa M, Inoda S, Asanuma H, Takasu H, Hasegawa T, Yasoshima T, Hirata K, Sato N.

Anticancer Res. 2013 Jan;33(1):167-73.


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