نتایج جستجو برای: aldrich

تعداد نتایج: 3555  

Journal: :iranian journal of allergy, asthma and immunology 0
sepideh safaei immunology, asthma and allergy research institute, tehran university of medical sciences, tehran, iran mohammad reza fazlollahi immunology, asthma and allergy research institute, tehran university of medical sciences, tehran, iran masoud houshmand national institute of genetic engineering biotechnology tehran, iran amir ali hamidieh hematology oncology & stem cell transplantation research center, tehran university of medical sciences, tehran, iran mohammad hassan bemanian department of pediatrics , division of allergy and clinical immunology, shahid sadoghi hospital, shahid sadoghi university of medical sciences, yazd, iran samin alavi department of pediatric hematology-oncology, mofid children's hospital, shahid beheshti university of medical sciences, tehran, iran

wiskott-aldrich syndrome (was) is a life-threatening x-linked recessive immunodeficiency disease described as a clinical triad of thrombocytopenia,  eczema, and recurrent infections, caused by mutations of the was protein (wasp) gene. the milder form of this disease is x-linked thrombocytopenia  (xlt) that  presents only as platelet abnormalities. mutation analysis for 15 boys with wiskott-aldr...

Journal: :international journal of pediatrics 0
kamleshun ramphul department of pediatrics, shanghai xin hua hospital affiliated to the shanghai jiao tong university school of medicine, china. sunjaye ramjuttun department of pediatrics, sir seewoosagur ramgoolam national hospital, mauritius, china. vinita poorun department of pediatrics, sir seewoosagur ramgoolam national hospital, mauritius, china.

wiskott-aldrich is an x-lined recessive disorder typically characterized by thrombocytopenia, eczema and recurrent infections. we report the four year treatment progress of a six year old boy who initially presented with vesicular lesions over the trunk, upper and lower extremities and face and blood tinged stools at the age of 2 weeks. from the family pedigree, there were two suspected cases t...

Journal: :The Annals of Iowa 1909

Kamleshun Ramphul, Sunjaye Ramjuttun Vinita Poorun

Wiskott-Aldrich is an X-lined recessive disorder typically characterized by thrombocytopenia, eczema and recurrent infections. We report the four year treatment progress of a six year old boy who initially presented with vesicular lesions over the trunk, upper and lower extremities and face and blood tinged stools at the age of 2 weeks. From the family pedigree, there were two suspected cases t...

Journal: :Psyche: A Journal of Entomology 1934

Journal: :PS: Political Science & Politics 2013

Journal: :Archives of Disease in Childhood 1967

2016
Shai Mangel Lothar Houben Maya Bar-Sadan

All the experiments in the paper were conducted using these materials : CdO (99.999%, Strem Chemicals, MA, USA), Se (99.999%, Alfa-Aesar, MA, USA), trioctylphosphine (TOP; 97%, SigmaAldrich, Israel), trioctylphosphine oxide (TOPO; 99%, Sigma-Aldrich, Israel), octadecylphosphonic acid (ODPA; 99%, Polycarbon Industries, MA, USA), S (99.98%, Sigma-Aldrich, Israel), oleic acid (90%, Alfa-Aesar, MA,...

Journal: :Haematologica 2012
Lee Macpherson James Monypenny Michael P Blundell Giles O Cory Jessica Tomé-García Adrian J Thrasher Gareth E Jones Yolanda Calle

Podosomes are actin-based adhesions involved in migration of cells that have to cross tissue boundaries such as myeloid cells. The Wiskott Aldrich Syndrome Protein regulates de novo actin polymerization during podosome formation and it is cleaved by the protease calpain during podosome disassembly. The mechanisms that may induce the Wiskott Aldrich Syndrome Protein cleavage by calpain remain un...

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2012

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