User profiles for ILSE WIELAND
Ilse Wielandapl. Professor of Human Genetics, Otto-von-Guericke University Magdeburg Verified email at med.ovgu.de Cited by 2715 |
[HTML][HTML] Mutations of the ephrin-B1 gene cause craniofrontonasal syndrome
I Wieland, S Jakubiczka, P Muschke, M Cohen… - The American Journal of …, 2004 - cell.com
Craniofrontonasal syndrome (CFNS) is an X-linked craniofacial disorder with an unusual
manifestation pattern, in which affected females show multiple skeletal malformations, whereas …
manifestation pattern, in which affected females show multiple skeletal malformations, whereas …
A novel member of the NF2/ERM/4.1 superfamily with growth suppressing properties in lung cancer
A novel putative tumor suppressor gene and member of the NF2/ERM/4.1 superfamily was
isolated using Differential Display PCR (DDPCR) on primary lung tumors. When reintroduced …
isolated using Differential Display PCR (DDPCR) on primary lung tumors. When reintroduced …
Microbeam MOMeNT: non-contact laser microdissection of membrane-mounted native tissue.
M Böhm, I Wieland, K Schütze… - The American journal of …, 1997 - ncbi.nlm.nih.gov
The analysis of tissue-specific genetic alterations depends on the selective procurement of
homogeneous cell populations. Microbeam microdissection of membrane-mounted native …
homogeneous cell populations. Microbeam microdissection of membrane-mounted native …
Expansion of the phenotypic spectrum and description of molecular findings in a cohort of patients with oculocutaneous mosaic RASopathies
…, M Pacheco‐Quito, I Wieland… - … Genetics & Genomic …, 2019 - Wiley Online Library
Background Postzygotic KRAS, HRAS, NRAS, and FGFR1 mutations result in a group of
mosaic RASopathies characterized by related developmental anomalies in eye, skin, heart, and …
mosaic RASopathies characterized by related developmental anomalies in eye, skin, heart, and …
Clinical and genetic aspects of craniofrontonasal syndrome: towards resolving a genetic paradox
P Wieacker, I Wieland - Molecular genetics and metabolism, 2005 - Elsevier
Craniofrontonasal syndrome (CFNS) is characterized by body asymmetry, midline defects,
skeletal abnormalities, and dermatological abnormalities. It is a very peculiar X-linked …
skeletal abnormalities, and dermatological abnormalities. It is a very peculiar X-linked …
[PDF][PDF] NFIB haploinsufficiency is associated with intellectual disability and macrocephaly
…, EH Sherr, C Smith-Hicks, I Wieland… - The American Journal of …, 2018 - cell.com
The nuclear factor I (NFI) family of transcription factors play an important role in normal
development of multiple organs. Three NFI family members are highly expressed in the brain, and …
development of multiple organs. Three NFI family members are highly expressed in the brain, and …
Twenty‐six novel EFNB1 mutations in familial and sporadic craniofrontonasal syndrome (CFNS)
Craniofrontonasal syndrome (CFNS) is an X‐linked disorder characterized by a more severe
manifestation in heterozygous females than in hemizygous males. Heterozygous females …
manifestation in heterozygous females than in hemizygous males. Heterozygous females …
Clinical and Genetic Evaluation of Patients with KATP Channel Mutations from the German Registry for Congenital Hyperinsulinism
K Mohnike, I Wieland, W Barthlen… - Hormone research in …, 2014 - karger.com
Congenital hyperinsulinism (CHI) causes hypoglycemia due to irregular insulin secretion. In
infants, a rapid diagnosis and appropriate management to avoid severe hypoglycemia is …
infants, a rapid diagnosis and appropriate management to avoid severe hypoglycemia is …
Differences of E-cadherin expression levels and patterns in primary and metastatic human lung cancer
M Böhm, B Totzeck, W Birchmeier, I Wieland - Clinical & experimental …, 1994 - Springer
Normal lung epithelium and 52 lung carcinomas obtained at surgical resection were
examined by immunofluorescence for their expression levels and patterns of the calcium-…
examined by immunofluorescence for their expression levels and patterns of the calcium-…
A method for difference cloning: gene amplification following subtractive hybridization.
I Wieland, G Bolger, G Asouline… - Proceedings of the …, 1990 - National Acad Sciences
We describe a procedure for genomic difference cloning, a method for isolating sequences
present in one genomic DNA population ("tester") that is absent in another ("driver"). By …
present in one genomic DNA population ("tester") that is absent in another ("driver"). By …