Macrophage invasion contributes to degeneration of stria vascularis in Pendred syndrome mouse model
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E. Green | P. Wangemann | S. Fleming | S. Wall | Ruchira Singh | Alisha Oelke | L. Everett | R. Maganti | S. Jabba
[1] E. Green,et al. Intercalated cell H+/OH- transporter expression is reduced in Slc26a4 null mice. , 2005, American journal of physiology. Renal physiology.
[2] R. Ransohoff,et al. Mononuclear phagocytes migrate into the murine cochlea after acoustic trauma , 2005, The Journal of comparative neurology.
[3] Kazuo Kobayashi,et al. Macrophages in inflammation. , 2005, Current drug targets. Inflammation and allergy.
[4] J. Segalés,et al. Histological Basis of the Porcine Femoral Artery for Vascular Research , 2005, Anatomia, histologia, embryologia.
[5] G. Firestein,et al. Innate Immunity Contributes to Cochlear Adaptive Immune Responses , 2004, Audiology and Neurotology.
[6] C. Petit,et al. Screening of SLC26A4 (PDS) gene in Pendred's syndrome: a large spectrum of mutations in France and phenotypic heterogeneity , 2004, Clinical genetics.
[7] E. Green,et al. Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model , 2004, BMC medicine.
[8] J. Ashmore,et al. Sugar Transport by Mammalian Members of the SLC26 Superfamily of Anion‐Bicarbonate Exchangers , 2003, The Journal of physiology.
[9] N. Hogg,et al. Rapid recruitment of inflammatory monocytes is independent of neutrophil migration. , 2003, Blood.
[10] E. Green,et al. Localization and Functional Studies of Pendrin in the Mouse Inner Ear Provide Insight About the Etiology of Deafness in Pendred Syndrome , 2003, Journal of the Association for Research in Otolaryngology.
[11] A. Moorman,et al. Assumption-free analysis of quantitative real-time polymerase chain reaction (PCR) data , 2003, Neuroscience Letters.
[12] E. Green,et al. Localization of pendrin in mouse kidney. , 2003, American journal of physiology. Renal physiology.
[13] J. A. Rillema,et al. Prolactin regulation of the pendrin-iodide transporter in the mammary gland. , 2003, American journal of physiology. Endocrinology and metabolism.
[14] E. Green,et al. Expression of PDS/Pds, the Pendred syndrome gene, in endometrium. , 2002, The Journal of clinical endocrinology and metabolism.
[15] M. Cohen-Salmon,et al. Spatiotemporal expression of otogelin in the developing and adult mouse inner ear , 2001, Hearing Research.
[16] E. Green,et al. Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretion , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[17] S. Filetti,et al. Na(+)/I(-) symporter and Pendred syndrome gene and protein expressions in human extra-thyroidal tissues. , 2001, European journal of endocrinology.
[18] E. Green,et al. Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome. , 2001, Human molecular genetics.
[19] V. Lazar,et al. The Journal of Clinical Endocrinology & Metabolism Printed in U.S.A. Copyright © 2000 by The Endocrine Society Expression of Pendrin and the Pendred Syndrome (PDS) , 2022 .
[20] W. Reardon,et al. Enlarged vestibular aqueduct: a radiological marker of pendred syndrome, and mutation of the PDS gene. , 2000, QJM : monthly journal of the Association of Physicians.
[21] E. Green,et al. Printed in U.S.A. Copyright © 2000 by The Endocrine Society Pendrin, the Protein Encoded by the Pendred Syndrome , 1999 .
[22] D. Scott,et al. Human pendrin expressed in Xenopus laevis oocytes mediates chloride/formate exchange. , 2000, American journal of physiology. Cell physiology.
[23] E. Green,et al. Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[24] Rong Wang,et al. The Pendred syndrome gene encodes a chloride-iodide transport protein , 1999, Nature Genetics.
[25] V. Sheffield,et al. Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS) , 1997, Nature Genetics.
[26] S. Heinemann,et al. Inner Ear Defects Induced by Null Mutationof the isk Gene , 1996, Neuron.
[27] L. Grammer. IMMUNOLOGY, 4TH EDITION , 1996 .
[28] P. Wangemann,et al. Ion transport mechanisms responsible for K+ secretion and the transepithelial voltage across marginal cells of stria vascularis in vitro , 1995, Hearing Research.
[29] G. Fraser,et al. Association of congenital deafness with goitre (Pendred's syndrome): A study of 207 families , 1964, Annals of human genetics.
[30] V. Pendred. DEAF-MUTISM AND GOITRE. , 1896 .