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Literature citations Results

Visual Pathways in Humans With Ephrin-B1 Deficiency Associated With the Cranio-Fronto-Nasal Syndrome.

Hoffmann M.B., Thieme H., Liedecke K., Meltendorf S., Zenker M., Wieland I.

Invest. Ophthalmol. Vis. Sci. 56:7427-7437(2015) · Mapped (1)

Twenty-six novel EFNB1 mutations in familial and sporadic craniofrontonasal syndrome (CFNS).

Wieland I., Reardon W., Jakubiczka S., Franco B., Kress W., Vincent-Delorme C., Thierry P., Edwards M., Koenig R., Rusu C. et al.

Hum. Mutat. 26:113-118(2005) · UniProtKB (1)

The impact of CFNS-causing EFNB1 mutations on ephrin-B1 function.

Makarov R., Steiner B., Gucev Z., Tasic V., Wieacker P., Wieland I.

BMC Med. Genet. 11:98-98(2010) · Mapped (1)

The heterozygous LMNA mutation p.R471G causes a variable phenotype with features of two types of familial partial lipodystrophy.

Muschke P., Kolsch U., Jakubiczka S., Wieland I., Brune T., Wieacker P.

Am. J. Med. Genet. A 143A:2810-2814(2007) · Mapped (10)

Specific mosaic KRAS mutations affecting codon 146 cause oculoectodermal syndrome and encephalocraniocutaneous lipomatosis.

Boppudi S., Bogershausen N., Hove H.B., Percin E.F., Aslan D., Dvorsky R., Kayhan G., Li Y., Cursiefen C., Tantcheva-Poor I. et al.

Clin. Genet. 90:334-342(2016) · Mapped (18)

Remission of congenital hyperinsulinism following conservative treatment: an exploratory study in patients with KATP channel mutations.

Lachmann M.J., Salgin B., Kummer S., Welters A., Doing C., Zenker M., Wieland I., Mayatepek E., Meissner T.

J. Pediatr. Endocrinol. Metab. 29:281-287(2016) · Mapped (13)

Promoter CpG hypermethylation and downregulation of DICE1 expression in prostate cancer.

Roepke A., Buhtz P., Boehm M., Seger J., Wieland I., Allhoff E.P., Wieacker P.F.

Oncogene 24:6667-6675(2005) · UniProtKB (1)

NFIB haploinsufficiency is associated with intellectual disability and macrocephaly.

Schanze I., Bunt J., Lim J.W.C., Schanze D., Dean R.J., Alders M., Blanchet P., Attie-Bitach T., Berland S., Boogert S. et al.

Am. J. Hum. Genet. 103:752-768(2018) · UniProtKB (2) · Mapped (7)

Mutations of the ephrin-B1 gene cause craniofrontonasal syndrome.

Wieland I., Jakubiczka S., Muschke P., Cohen M., Thiele H., Gerlach K.L., Adams R.H., Wieacker P.

Am. J. Hum. Genet. 74:1209-1215(2004) · UniProtKB (1)

Molecular interactions of B-CAM (basal-cell adhesion molecule) and laminin in epithelial skin cancer.

Drewniok C., Wienrich B.G., Schon M., Ulrich J., Zen Q., Telen M.J., Hartig R.J., Wieland I., Gollnick H., Schon M.P.

Arch. Dermatol. Res. 296:59-66(2004) · Mapped (22)

Molecular characterization of the DICE1 (DDX26) tumor suppressor gene in lung carcinoma cells.

Wieland I., Roepke A., Stumm M., Sell C., Weidle U.H., Wieacker P.F.

Oncol. Res. 12:491-500(2001) · UniProtKB (1) · Mapped (6)

Isolation of DICE1: a gene frequently affected by LOH and downregulated in lung carcinomas.

Wieland I., Arden K.C., Michels D., Klein-Hitpass L., Boehm M., Viars C.S., Weidle U.H.

Oncogene 18:4530-4537(1999) · UniProtKB (1)

Inhibitor-Immunology-Study. Different HLA-types seem to be involved in the inhibitor development in haemophilia A.

Wieland I., Wermes C., Eifrig B., Holstein K., Pollmann H., Siegmund B., Bidlingmaier C., Kurnik K., Nimtz-Talaska A., Niekrens C. et al.

Hamostaseologie 28 Suppl 1:S26-8(2008) · Mapped (21,805)

Genetic Variants of DICE1/INTS6 in German Prostate Cancer Families with Linkage to 13q14.

Bohm M., Maier C., Kufer R., Ropke A., Vogel W., Wieland I.

Urol. Int. 95:386-389(2015) · Mapped (7)

Ectopic expression of DICE1 suppresses tumor cell growth.

Wieland I., Sell C., Weidle U.H., Wieacker P.

Oncol. Rep. 12:207-211(2004) · UniProtKB (1) · Mapped (17)

Dissecting the molecular mechanisms in craniofrontonasal syndrome: differential mRNA expression of mutant EFNB1 and the cellular mosaic.

Wieland I., Makarov R., Reardon W., Tinschert S., Goldenberg A., Thierry P., Wieacker P.

Eur. J. Hum. Genet. 16:184-191(2008) · Mapped (1)

Detection of a multilineage mosaic NRAS mutation c.181C>A (p.Gln61Lys) in an individual with a complex congenital nevus syndrome.

Ulrich M., Tinschert S., Siebert E., Franke I., Tuting T., Ulrich J., Schanze D., Wieland I., Zenker M.

Pigment Cell Melanoma Res 32:470-473(2019) · Mapped (5)

Cloning and characterization of CAP, the S. cerevisiae gene encoding the 70 kd adenylyl cyclase-associated protein.

Field J., Vojtek A., Ballester R., Bolger G., Colicelli J., Ferguson K., Gerst J., Kataoka T., Michaeli T., Powers S. et al.

Cell 61:319-327(1990) · UniProtKB (1)

Clinical and genetic evaluation of patients with KATP channel mutations from the German registry for congenital hyperinsulinism.

Mohnike K., Wieland I., Barthlen W., Vogelgesang S., Empting S., Mohnike W., Meissner T., Zenker M.

Horm Res Paediatr 81:156-168(2014) · Mapped (13)

A Postzygotic SMO Mutation Caused the Original Case of Happle-Tinschert Syndrome.

Zenker M., Tinschert S., Wieland I., Schanze D., Happle R.

Acta Derm. Venereol. 98:534-535(2018) · Mapped (3)

A novel member of the NF2/ERM/4.1 superfamily with growth suppressing properties in lung cancer.

Tran Y.K., Boegler O., Gorse K.M., Wieland I., Green M.R., Newsham I.F.

Cancer Res. 59:35-43(1999) · UniProtKB (1)

A missense mutation in the coiled-coil motif of the HP1-interacting domain of ATR-X in a family with X-linked mental retardation.

Wieland I., Sabathil J., Ostendorf A., Rittinger O., Roepke A., Winnepenninckx B., Kooy F., Holinski-Feder E., Wieacker P.

Neurogenetics 6:45-47(2005) · UniProtKB (1)

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