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1999 1
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Page 1
Leukocyte adhesion deficiency type II.
Becker DJ, Lowe JB. Becker DJ, et al. Biochim Biophys Acta. 1999 Oct 8;1455(2-3):193-204. doi: 10.1016/s0925-4439(99)00071-x. Biochim Biophys Acta. 1999. PMID: 10571012 Free article. Review.
Leukocyte adhesion deficiency type II (LAD II) is a rare disorder characterized by recurrent infections, persistent leukocytosis, and severe mental and growth retardation. ...However, the two known component enzymes in this GDP-fuc …
Leukocyte adhesion deficiency type II (LAD II) is a rare disorder characterized by recurren …
Leukocyte adhesion deficiencies.
van de Vijver E, van den Berg TK, Kuijpers TW. van de Vijver E, et al. Hematol Oncol Clin North Am. 2013 Feb;27(1):101-16, viii. doi: 10.1016/j.hoc.2012.10.001. Epub 2012 Nov 13. Hematol Oncol Clin North Am. 2013. PMID: 23351991 Review.
Leukocytes migrate to the site of inflammation by crawling over and through the blood vessel wall, into the tissue. Leukocyte adhesion deficiencies (ie, LAD-I, -II, and LAD-I/variant, the latter also known as LAD-III) are caused by defects in the adhesion …
Leukocytes migrate to the site of inflammation by crawling over and through the blood vessel wall, into the tissue. Leukocyte adhe …
Leukocyte adhesion deficiency type II: long-term follow-up and review of the literature.
Gazit Y, Mory A, Etzioni A, Frydman M, Scheuerman O, Gershoni-Baruch R, Garty BZ. Gazit Y, et al. J Clin Immunol. 2010 Mar;30(2):308-13. doi: 10.1007/s10875-009-9354-0. Epub 2010 Jan 23. J Clin Immunol. 2010. PMID: 20099014 Review.
INTRODUCTION: Leukocyte adhesion deficiency (LAD) is a group of rare inherited disorders characterized by immune deficiency and peripheral neutrophilia. There are only seven reported cases of LAD type II worldwide, and no long-term follow …
INTRODUCTION: Leukocyte adhesion deficiency (LAD) is a group of rare inherited disorders characterized by immune def …
Defining the mild variant of leukocyte adhesion deficiency type II (SLC35C1-congenital disorder of glycosylation) and response to l-fucose therapy: Insights from two new families and review of the literature.
Tahata S, Raymond K, Quade M, Barnes S, Boyer S, League S, Kumanovics A, Abraham R, Jacob E, Menon P, Morava E. Tahata S, et al. Am J Med Genet A. 2022 Jul;188(7):2005-2018. doi: 10.1002/ajmg.a.62737. Epub 2022 Mar 26. Am J Med Genet A. 2022. PMID: 35338746 Review.
Leukocyte adhesion deficiency type II (LAD II, also known as SLC35C1-congenital disorder of glycosylation) is an autosomal recessive disorder characterized by growth and cognitive impairment, peripheral neutrop …
Leukocyte adhesion deficiency type II (LAD II, also known as SLC35C1-congenital disorder …
Biological functions of fucose in mammals.
Schneider M, Al-Shareffi E, Haltiwanger RS. Schneider M, et al. Glycobiology. 2017 Jul 1;27(7):601-618. doi: 10.1093/glycob/cwx034. Glycobiology. 2017. PMID: 28430973 Free PMC article. Review.
Fucose modifications have also been implicated in many other biological functions including immunity and cancer. Congenital mutations of a Golgi apparatus localized GDP-fucose transporter causes leukocyte adhesion deficiency type II, whic …
Fucose modifications have also been implicated in many other biological functions including immunity and cancer. Congenital mutations …
Fucose: biosynthesis and biological function in mammals.
Becker DJ, Lowe JB. Becker DJ, et al. Glycobiology. 2003 Jul;13(7):41R-53R. doi: 10.1093/glycob/cwg054. Epub 2003 Mar 19. Glycobiology. 2003. PMID: 12651883 Review.
In mammals, fucose-containing glycans have important roles in blood transfusion reactions, selectin-mediated leukocyte-endothelial adhesion, host-microbe interactions, and numerous ontogenic events, including signaling events by the Notch receptor family. Alteration …
In mammals, fucose-containing glycans have important roles in blood transfusion reactions, selectin-mediated leukocyte-endothelial …
Congenital disorders involving defective N-glycosylation of proteins.
Schachter H. Schachter H. Cell Mol Life Sci. 2001 Jul;58(8):1085-104. doi: 10.1007/PL00000923. Cell Mol Life Sci. 2001. PMID: 11529501 Review.
Hereditary erythroblastic multinuclearity with a positive acidified-serum lysis test (HEMPAS; congenital dyserythropoietic anemia type II) presents as a relatively mild dyserythropoietic anemia. The genetic defect in most cases of HEMPAS is not known, but alp …
Hereditary erythroblastic multinuclearity with a positive acidified-serum lysis test (HEMPAS; congenital dyserythropoietic anemia …
Molecular physiology and pathology of the nucleotide sugar transporter family (SLC35).
Ishida N, Kawakita M. Ishida N, et al. Pflugers Arch. 2004 Feb;447(5):768-75. doi: 10.1007/s00424-003-1093-0. Epub 2003 May 21. Pflugers Arch. 2004. PMID: 12759756 Review.
Pathological analyses and developmental studies of small, multicellular organisms deficient in nucleotide sugar transporters have shown these transporters to be involved in tumour metastasis, cellular immunity, organogenesis and morphogenesis. Leukocyte adhesion …
Pathological analyses and developmental studies of small, multicellular organisms deficient in nucleotide sugar transporters have shown thes …
Human deficiencies of fucosylation and sialylation affecting selectin ligands.
Lühn K, Wild MK. Lühn K, et al. Semin Immunopathol. 2012 May;34(3):383-99. doi: 10.1007/s00281-012-0304-1. Epub 2012 Mar 31. Semin Immunopathol. 2012. PMID: 22461019 Review.
Selectins are carbohydrate-binding adhesion molecules that are required for leukocyte trafficking to secondary lymphoid organs and to sites of infection. ...However, as this review shows, the picture appears to be more complex and more interesting. Although there ar …
Selectins are carbohydrate-binding adhesion molecules that are required for leukocyte trafficking to secondary lymphoid organs …
[Leukocyte adhesion deficiency, type II].
Kawamura N, Kobayashi K. Kawamura N, et al. Ryoikibetsu Shokogun Shirizu. 2000;(32):173-6. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11212680 Review. Japanese. No abstract available.
11 results