1 - 25 of 60 results for author:"Omran H." in Literature citations
Results Customize
› Repeat search in UniProtKB (67)
| The nexin-dynein regulatory complex subunit DRC1 is essential for motile cilia function in algae and humans. Wirschell M., Olbrich H., Werner C., Tritschler D., Bower R., Sale W.S., Loges N.T., Pennekamp P., Lindberg S., Stenram U. et al. Nat. Genet. 45:262-268(2013) · UniProtKB (3) |
| Downregulation of IL-17-producing T cells is associated with regulatory T cell expansion and disease progression in chronic lymphocytic leukemia. Jadidi-Niaragh F., Ghalamfarsa G., Memarian A., Asgarian-Omran H., Razavi S.M., Sarrafnejad A., Shokri F. Tumour Biol. 34:929-940(2013) · Mapped (3) |
| Structural characterization of bacterioferritin from Blastochloris viridis. Wahlgren W.Y., Omran H., von Stetten D., Royant A., van der Post S., Katona G. PLoS ONE 7:e46992-e46992(2012) · UniProtKB (1) |
| Recessive HYDIN mutations cause primary ciliary dyskinesia without randomization of left-right body asymmetry. Olbrich H., Schmidts M., Werner C., Onoufriadis A., Loges N.T., Raidt J., Banki N.F., Shoemark A., Burgoyne T., Al Turki S. et al. Am. J. Hum. Genet. 91:672-684(2012) · UniProtKB (2) |
| Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling. Chaki M., Airik R., Ghosh A.K., Giles R.H., Chen R., Slaats G.G., Wang H., Hurd T.W., Zhou W., Cluckey A. et al. |
| CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms. Panizzi J.R., Becker-Heck A., Castleman V.H., Al-Mutairi D.A., Liu Y., Loges N.T., Pathak N., Austin-Tse C., Sheridan E., Schmidts M. et al. Nat. Genet. 44:714-719(2012) · UniProtKB (3) |
| Mutations in axonemal dynein assembly factor DNAAF3 cause primary ciliary dyskinesia. Mitchison H.M., Schmidts M., Loges N.T., Freshour J., Dritsoula A., Hirst R.A., O'Callaghan C., Blau H., Al Dabbagh M., Olbrich H. et al. |
| Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructure. Genetic Disorders of Mucociliary Clearance Consortium |
| U1 snRNA-mediated gene therapeutic correction of splice defects caused by an exceptionally mild BBS mutation. Schmid F., Glaus E., Barthelmes D., Fliegauf M., Gaspar H., Nurnberg G., Nurnberg P., Omran H., Berger W., Neidhardt J. Hum. Mutat. 32:815-824(2011) · Mapped (8) |
| Oncogenic FAM131B-BRAF fusion resulting from 7q34 deletion comprises an alternative mechanism of MAPK pathway activation in pilocytic astrocytoma. Cin H., Meyer C., Herr R., Janzarik W.G., Lambert S., Jones D.T., Jacob K., Benner A., Witt H., Remke M. et al. Acta Neuropathol. 121:763-774(2011) · Mapped (3) |
| The molecular basis of aminoacylase 1 deficiency. Sommer A., Christensen E., Schwenger S., Seul R., Haas D., Olbrich H., Omran H., Sass J.O. Biochim. Biophys. Acta 1812:685-690(2011) · UniProtKB (1) · Mapped (4) |
| Analysis of BRAF V600E mutation in 1,320 nervous system tumors reveals high mutation frequencies in pleomorphic xanthoastrocytoma, ganglioglioma and extra-cerebellar pilocytic astrocytoma. Schindler G., Capper D., Meyer J., Janzarik W., Omran H., Herold-Mende C., Schmieder K., Wesseling P., Mawrin C., Hasselblatt M. et al. Acta Neuropathol. 121:397-405(2011) · Mapped (3) |
| Functional characterization of a BRAF insertion mutant associated with pilocytic astrocytoma. Eisenhardt A.E., Olbrich H., Roring M., Janzarik W., Anh T.N., Cin H., Remke M., Witt H., Korshunov A., Pfister S.M. et al. Int. J. Cancer 129:2297-2303(2011) · Mapped (3) |
| The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation. Becker-Heck A., Zohn I.E., Okabe N., Pollock A., Lenhart K.B., Sullivan-Brown J., McSheene J., Loges N.T., Olbrich H., Haeffner K. et al. |
| CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs. Merveille A.C., Davis E.E., Becker-Heck A., Legendre M., Amirav I., Bataille G., Belmont J., Beydon N., Billen F., Clement A. et al. Nat. Genet. 43:72-78(2011) · UniProtKB (6) |
| Mucopolysaccharidosis type IIID: 12 new patients and 15 novel mutations. Valstar M.J., Bertoli-Avella A.M., Wessels M.W., Ruijter G.J.G., de Graaf B., Olmer R., Elfferich P., Neijs S., Kariminejad R., Suheyl Ezgue F. et al. Hum. Mutat. 31:E1348-E1360(2010) · UniProtKB (1) · Mapped (7) |
| Novel integrin-dependent platelet malfunction in siblings with leukocyte adhesion deficiency-III (LAD-III) caused by a point mutation in FERMT3. Jurk K., Schulz A.S., Kehrel B.E., Rapple D., Schulze H., Mobest D., Friedrich W.W., Omran H., Deak E., Henschler R. et al. Thromb. Haemost. 103:1053-1064(2010) · Mapped (1) |
| Deletions and point mutations of LRRC50 cause primary ciliary dyskinesia due to dynein arm defects. Loges N.T., Olbrich H., Becker-Heck A., Haffner K., Heer A., Reinhard C., Schmidts M., Kispert A., Zariwala M.A., Leigh M.W. et al. Am. J. Hum. Genet. 85:883-889(2009) · UniProtKB (1) · Mapped (1) |
| Variation in WNT genes expression in different subtypes of chronic lymphocytic leukemia. Memarian A., Hojjat-Farsangi M., Asgarian-Omran H., Younesi V., Jeddi-Tehrani M., Sharifian R.A., Khoshnoodi J., Razavi S.M., Rabbani H., Shokri F. Leuk. Lymphoma 50:2061-2070(2009) · Mapped (18) |
| Initiation and maturation of cilia-generated flow in newborn and postnatal mouse airway. Francis R.J., Chatterjee B., Loges N.T., Zentgraf H., Omran H., Lo C.W. Am. J. Physiol. Lung Cell Mol. Physiol. 296:L1067-75(2009) · Mapped (3) |
| How useful is determination of anti-factor Xa activity to guide bridging therapy with enoxaparin? A pilot study. Hammerstingl C., Omran H., Tripp C., Poetzsch B. Thromb. Haemost. 101:325-332(2009) · Mapped (3) |
| Ktu/PF13 is required for cytoplasmic pre-assembly of axonemal dyneins. Omran H., Kobayashi D., Olbrich H., Tsukahara T., Loges N.T., Hagiwara H., Zhang Q., Leblond G., O'Toole E., Hara C. et al. |
| Refining the phenotype of alpha-1a Tubulin (TUBA1A) mutation in patients with classical lissencephaly. Morris-Rosendahl D.J., Najm J., Lachmeijer A.M., Sztriha L., Martins M., Kuechler A., Haug V., Zeschnigk C., Martin P., Santos M. et al. Clin. Genet. 74:425-433(2008) · Mapped (5) |
| DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein arm. Loges N.T., Olbrich H., Fenske L., Mussaffi H., Horvath J., Fliegauf M., Kuhl H., Baktai G., Peterffy E., Chodhari R. et al. Am. J. Hum. Genet. 83:547-558(2008) · UniProtKB (1) · Mapped (1) |
| Low representation of Fc receptor-like 1-5 molecules in leukemic cells from Iranian patients with acute lymphoblastic leukemia. Kazemi T., Asgarian-Omran H., Memarian A., Shabani M., Sharifian R.A., Vossough P., Ansaripour B., Rabbani H., Shokri F. Cancer Immunol. Immunother. 58:989-996(2009) · Mapped (7) |