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Klaus Wrogemann

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Sarah Nicklas; Anthony Otto; Ketan Patel; Sandra Stelzer; Yefei Wen; Klaus Wrogemann; Xiaoli Wu; Hao Ding; Shihuan Kuang; Pamela Miller; Jens C Schwamborn
TRIM32 regulates skeletal muscle stem cell differentiation and is necessary for normal adult muscle regeneration.
Gertrud Strobl-Wildemann; Hao Hu; Vera M Kalscheuer; Hans-Hilger Ropers; Klaus Wrogemann; Andreas Tzschach
Novel GDI1 mutation in a large family with nonsyndromic X-linked intellectual disability.
Hao Hu; Tim B Hucho; Kimia Kahrizi; Ideh Bahman; Wei Chen; Katinka Eggers; Masoud Garshasbi; Rita Gerardy-Schahn; Masoumeh Hosseini; Mohammad Mahdi Motazacker; Martina Mühlenhoff; Hossein Najmabadi; H Hilger Ropers; Andreas Tzschach; Klaus Wrogemann; Andreas W Kuss
ST3GAL3 mutations impair the development of higher cognitive functions.

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2012: Sarah Nicklas; Anthony Otto; Ketan Patel; Sandra Stelzer; Yefei Wen; Klaus Wrogemann; Xiaoli Wu; Hao Ding; Shihuan Kuang; Pamela Miller; Jens C Schwamborn
TRIM32 regulates skeletal muscle stem cell differentiation and is necessary for normal adult muscle regeneration.
PloS one 2012;7(1):e30445.
2011: Gertrud Strobl-Wildemann; Hao Hu; Vera M Kalscheuer; Hans-Hilger Ropers; Klaus Wrogemann; Andreas Tzschach
Novel GDI1 mutation in a large family with nonsyndromic X-linked intellectual disability.
American journal of medical genetics. Part A 2011;155A(12):3067-70.
2011: Hao Hu; Tim B Hucho; Kimia Kahrizi; Ideh Bahman; Wei Chen; Katinka Eggers; Masoud Garshasbi; Rita Gerardy-Schahn; Masoumeh Hosseini; Mohammad Mahdi Motazacker; Martina Mühlenhoff; Hossein Najmabadi; H Hilger Ropers; Andreas Tzschach; Klaus Wrogemann; Andreas W Kuss
ST3GAL3 mutations impair the development of higher cognitive functions.
American journal of human genetics 2011;89(3):407-14.
2009: Hao Hu; Vera Kalscheuer; Corinna Menzel; Martine Raynaud; Hugues Richard; Hilger Ropers; Andreas Tzschach; Hans Van Bokhoven; Klaus Wrogemann; Melanie Bienek; Jamel Chelly; Guy Froyen; Stefan A Haas; Wei Chen
Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing.
The HUGO journal 2009;3(1-4):41-9.
2009: Hao Hu; Klaus Wrogemann; Vera Kalscheuer; Andreas Tzschach; Hugues Richard; Stefan A Haas; Corinna Menzel; Melanie Bienek; Guy Froyen; Martine Raynaud; Hans Van Bokhoven; Jamel Chelly; Hilger Ropers; Wei Chen
Erratum to: Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing.
The HUGO journal 2009;3(1-4):83.
2009: Kristian Borg; Rolf Stucka; Matthew Locke; Eva Melin; Gabrielle Ahlberg; Ursula Klutzny; Maja von der Hagen; Angela Huebner; Hanns Lochmüller; Klaus Wrogemann; Lars-Eric Thornell; Derek J Blake; Benedikt Schoser
Intragenic deletion of TRIM32 in compound heterozygotes with sarcotubular myopathy/LGMD2H.
Human mutation 2009;30(9):E831-44.
2009: Joy Armistead; Sunita Khatkar; Britta Meyer; Brian L Mark; Nehal Patel; Gail Coghlan; Ryan E Lamont; Shuangbo Liu; Jill Wiechert; Peter A Cattini; Peter Koetter; Klaus Wrogemann; Cheryl R Greenberg; Karl-Dieter Entian; Teresa Zelinski; Barbara L Triggs-Raine
Mutation of a gene essential for ribosome biogenesis, EMG1, causes Bowen-Conradi syndrome.
American journal of human genetics 2009;84(6):728-39.
2006: Amador Albor; Sally El-Hizawi; Elizabeth J Horn; Melanie Laederich; Patrick Frosk; Klaus Wrogemann; Molly Kulesz-Martin
The interaction of Piasy with Trim32, an E3-ubiquitin ligase mutated in limb-girdle muscular dystrophy type 2H, promotes Piasy degradation and regulates UVB-induced keratinocyte apoptosis through NFkappaB.
The Journal of biological chemistry 2006;281(35):25850-66.
2005: Patrick Frosk; Marc R Del Bigio; Klaus Wrogemann; Cheryl R Greenberg
Hutterite brothers both affected with two forms of limb girdle muscular dystrophy: LGMD2H and LGMD2I.
European journal of human genetics : EJHG 2005;13(8):978-82.
2005: Benedikt Schoser; Patrick Frosk; Andrew G Engel; Ursula Klutzny; Hanns Lochmüller; Klaus Wrogemann
Commonality of TRIM32 mutation in causing sarcotubular myopathy and LGMD2H.
Annals of neurology 2005;57(4):591-5.
2005: Ryan E Lamont; J Concepción Loredo-Osti; Nicole M Roslin; Jill Mauthe; Gail Coghlan; Edward Nylen; Danielle Frappier; A Micheil Innes; Edmond G Lemire; R Brian Lowry; Cheryl R Greenberg; Barbara L Triggs-Raine; Kenneth Morgan; Klaus Wrogemann; T Mary Fujiwara; Teresa Zelinski
A locus for Bowen-Conradi syndrome maps to chromosome region 12p13.3.
American journal of medical genetics. Part A 2005;132A(2):136-43.
2005: Patrick Frosk; Cheryl R Greenberg; Alysa A P Tennese; Ryan Lamont; Edward Nylen; Cheryl J A Hirst; Danielle Frappier; Nicole M Roslin; Michaela Zaik; Kate Bushby; Volker Straub; Mayana Zatz; Flavia de Paula; Kenneth Morgan; T Mary Fujiwara; Klaus Wrogemann
The most common mutation in FKRP causing limb girdle muscular dystrophy type 2I (LGMD2I) may have occurred only once and is present in Hutterites and other populations.
Human mutation 2005;25(1):38-44.
2004: Maja Poppe; John Bourke; Michelle Eagle; Patrick Frosk; Klaus Wrogemann; Cheryl Greenberg; Francesco Muntoni; Thomas Voit; Volker Straub; David Hilton-Jones; Cheerag Shirodaria; Kate Bushby
Cardiac and respiratory failure in limb-girdle muscular dystrophy 2I.
Annals of neurology 2004;56(5):738-41.
2002: Patrick Frosk; Tracey Weiler; Edward Nylen; Thangirala Sudha; Cheryl R Greenberg; Kenneth Morgan; T Mary Fujiwara; Klaus Wrogemann
Limb-girdle muscular dystrophy type 2H associated with mutation in TRIM32, a putative E3-ubiquitin-ligase gene.
American journal of human genetics 2002;70(3):663-72.
2002: K Leriche-Guérin; Louise V B Anderson; Klaus Wrogemann; Brigitte Roy; Marlyne Goulet; Jacques P Tremblay
Dysferlin expression after normal myoblast transplantation in SCID and in SJL mice.
Neuromuscular disorders : NMD 2002;12(2):167-73.
2000: Sergei N Illarioshkin; Irina A Ivanova-Smolenskaya; Cheryl R Greenberg; Edward Nylen; V S Sukhorukov; VV Poleshchuk; Elena D Markova; Klaus Wrogemann
Identical dysferlin mutation in limb-girdle muscular dystrophy type 2B and distal myopathy.
Neurology 2000;55(12):1931-3.
2000: Louise V B Anderson; R M Harrison; R Pogue; E Vafiadaki; C Pollitt; K Davison; JA Moss; Sharon M Keers; Angela Pyle; Pamela J Shaw; Ibrahim Mahjneh; Zohar Argov; Cheryl R Greenberg; Klaus Wrogemann; Tulio Bertorini; H H Goebel; Jacques Beckmann; Rumaisa Bashir; K M D Bushby
Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies).
Neuromuscular disorders : NMD 2000;10(8):553-9.
1999: Tracey Weiler; Rumaisa Bashir; Louise V B Anderson; K Davison; JA Moss; S Britton; Edward Nylen; Sharon M Keers; E Vafiadaki; Cheryl R Greenberg; C R Bushby; Klaus Wrogemann
Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s).
Human molecular genetics 1999;8(5):871-7.
1998: Tracey Weiler; Cheryl R Greenberg; Teresa Zelinski; Edward Nylen; Gail Coghlan; MJ Crumley; T Mary Fujiwara; Kenneth Morgan; Klaus Wrogemann
A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus.
American journal of human genetics 1998;63(1):140-7.
1997: Tracey Weiler; Cheryl R Greenberg; Edward Nylen; Kenneth Morgan; T Mary Fujiwara; MJ Crumley; Teresa Zelinski; William C Halliday; Barbara E Nickel; Barbara L Triggs-Raine; Klaus Wrogemann
Limb girdle muscular dystrophy in Manitoba Hutterites does not map to any of the known LGMD loci.
American journal of medical genetics 1997;72(3):363-8.
1996: Tracey Weiler; Cheryl R Greenberg; Edward Nylen; William C Halliday; Kenneth Morgan; D Eggertson; Klaus Wrogemann
Limb-girdle muscular dystrophy and Miyoshi myopathy in an aboriginal Canadian kindred map to LGMD2B and segregate with the same haplotype.
American journal of human genetics 1996;59(4):872-8.
1996: K D Serfas; Deepak Bose; L Patel; Klaus Wrogemann; M S Phillips; D H MacLennan; Cheryl R Greenberg
Comparison of the segregation of the RYR1 C1840T mutation with segregation of the caffeine/halothane contracture test results for malignant hyperthermia susceptibility in a large Manitoba Mennonite family.
Anesthesiology 1996;84(2):322-9.
1995: D D Belsham; F Pereira; Cheryl R Greenberg; S Liao; Klaus Wrogemann
Leu-676-Pro mutation of the androgen receptor causes complete androgen insensitivity syndrome in a large Hutterite kindred.
Human mutation 1995;5(1):28-33.
1993: E Hildes; H K Jacobs; A Cameron; S S Seshia; F Booth; Jane A Evans; Klaus Wrogemann; Cheryl R Greenberg
Impact of genetic counselling after neonatal screening for Duchenne muscular dystrophy.
Journal of medical genetics 1993;30(8):670-4.
1993: E J Keely; D D Belsham; Klaus Wrogemann; C Faiman
Partial androgen insensitivity--are all tissues equal?
Fertility and sterility 1993;60(2):366-8.
1993: F P Bernier; Cheryl R Greenberg; William C Halliday; Klaus Wrogemann
Single-blind study of dystrophin staining in carriers of Duchenne muscular dystrophy.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 1993;20(1):44-7.
1993: F A Pereira; E Rosenmann; Edward Nylen; Klaus Wrogemann
Human cytosolic aldehyde dehydrogenase in androgen insensitivity syndrome.
Advances in experimental medicine and biology 1993;328():45-50.
1992: D D Belsham; W C Yee; Cheryl R Greenberg; Klaus Wrogemann
Analysis of the CAG repeat region of the androgen receptor gene in a kindred with X-linked spinal and bulbar muscular atrophy.
Journal of the neurological sciences 1992;112(1-2):133-8.
1991: Klaus Wrogemann; G Podolsky; J Gu; E Rosenmann
A 63-kDa protein with androgen-binding activity is not from the androgen receptor.
Biochemistry and cell biology = Biochimie et biologie cellulaire 1991;69(10-11):695-701.
1991: Mark Trifiro; R L Prior; N Sabbaghian; Leonard Pinsky; M Kaufman; Edward Nylen; D D Belsham; Cheryl R Greenberg; Klaus Wrogemann
Amber mutation creates a diagnostic MaeI site in the androgen receptor gene of a family with complete androgen insensitivity.
American journal of medical genetics 1991;40(4):493-9.
1991: Cheryl R Greenberg; H K Jacobs; William C Halliday; Klaus Wrogemann
Three years' experience with neonatal screening for Duchenne/Becker muscular dystrophy: gene analysis, gene expression, and phenotype prediction.
American journal of medical genetics 1991;39(1):68-75.
1991: F Pereira; E Rosenmann; Edward Nylen; M Kaufman; Leonard Pinsky; Klaus Wrogemann
The 56 kDa androgen binding protein is an aldehyde dehydrogenase.
Biochemical and biophysical research communications 1991;175(3):831-8.
1991: Mark Trifiro; Bruce Gottlieb; Leonard Pinsky; M Kaufman; L Prior; D D Belsham; Klaus Wrogemann; C J Brown; H F Willard; J Trapman
The 56/58 kDa androgen-binding protein in male genital skin fibroblasts with a deleted androgen receptor gene.
Molecular and cellular endocrinology 1991;75(1):37-47.
1990: F Pereira; D Belsham; K Duerksen; E Rosenmann; M Kaufman; Leonard Pinsky; Klaus Wrogemann
The 56 kDa androgen-binding protein in human genital skin fibroblasts: its relation to the human androgen receptor.
Molecular and cellular endocrinology 1990;68(2-3):195-204.
1989: D D Belsham; E Rosenmann; F A Pereira; S G Williams; Maxine K Turney; William Kovacs; L E Faber; Klaus Wrogemann
The 56 kDa protein of human genital skin fibroblasts is identical to that radiolabelled by [3H]dihydrotestosterone 17 beta-bromoacetate.
Journal of steroid biochemistry 1989;33(3):389-94.
1988: Klaus Wrogemann; F Pereira; D Belsham; M Kaufman; Leonard Pinsky; E Rosenmann
An abundant 56 kD protein with low affinity androgen binding: another member of the steroid/thyroid receptor family?
Biochemical and biophysical research communications 1988;155(2):907-13.
1988: Cheryl R Greenberg; M Rohringer; H K Jacobs; N Averill; Edward Nylen; G J van Ommen; Klaus Wrogemann
Gene studies in newborn males with Duchenne muscular dystrophy detected by neonatal screening.
Lancet 1988;2(8608):425-7.
1988: M J Glesby; E Rosenmann; Edward Nylen; Klaus Wrogemann
Serum CK, calcium, magnesium, and oxidative phosphorylation in mdx mouse muscular dystrophy.
Muscle & nerve 1988;11(8):852-6.
1988: B Nickel; A Schwartz; E Rosenmann; M Kaufman; Leonard Pinsky; Klaus Wrogemann
A study of androgen-resistant subjects indicates that the 6.7 pI/56 kDa protein in genital skin fibroblasts is related to the androgen receptor.
Clinical and investigative medicine. Médecine clinique et experimentale 1988;11(1):22-33.
1987: I Oberlé; G Camerino; Klaus Wrogemann; B Arveiler; André Hanauer; E Raimondi; Jean-Louis Mandel
Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27.
Human genetics 1987;77(1):60-5.
1987: Cheryl R Greenberg; J L Hamerton; M Nigli; Klaus Wrogemann
DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21.
American journal of human genetics 1987;41(2):128-37.
1986: Klaus Wrogemann; B Arveiler; I Oberle; L M Mulligan; J A Holden; C J Forster-Gibson; B N White
A TaqI RFLP in Xq26-Xqter detected by pX45h [HGM8 no. DXS100h].
Nucleic acids research 1986;14(13):5572.
1986: Louis Kunkel; J Fielding Hejtmancik; C T Caskey; Astrid Speer; Anthony P Monaco; W Middlesworth; C A Colletti; C Bertelson; U Müller; M Bresnan; F Shapiro; U Tantravahi; J Speer; S A Latt; R Bartlett; Margaret Pericak-Vance; Allen D Roses; M W Thompson; P N Ray; R G Worton; Kenneth H Fischbeck; Pía Gallano; M Coulon; C Duros; J Boue; Claudine Junien; Jamel Chelly; G Hamard; Marc Jeanpierre; M Lambert; Jean-Claude Kaplan; A Emery; H Dorkins; S McGlade; Kay E Davies; Corinne D Boehm; B Arveiler; C Lemaire; G J Morgan; M J Denton; J Amos; Martin Bobrow; F Benham; E Boswinkel; C Cole; Victor Dubowitz; K Hart; S Hodgson; L Johnson; A Walker; L Roncuzzi; Alessandra Ferlini; C Nobile; Giovanni Romeo; D E Wilcox; N A Affara; M A Ferguson-Smith; M Lindolf; H Kaariainen; A de la Chapelle; V Ionasescu; Charles C Searby; R Ionasescu; Egbert Bakker; Gert-Jan B van Ommen; P L Pearson; Cheryl R Greenberg; J L Hamerton; Klaus Wrogemann; R A Doherty; R Polakowska; C Hyser; S Quirk; N Thomas; Jeffrey F Harper; B T Darras; U Francke
Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy.
Nature 1986;322(6074):73-7.
1986: D C Riddell; H S Wang; J Beckett; A Chan; J J Holden; L M Mulligan; M A Phillips; N E Simpson; Klaus Wrogemann; J L Hamerton
Regional localization of 18 human X-linked DNA sequences.
Cytogenetics and cell genetics 1986;42(3):123-8.
1985: Klaus Wrogemann; Edward Nylen; I Adamson; S V Pande
Functional studies on in situ-like mitochondria isolated in the presence of polyvinyl pyrrolidone.
Biochimica et biophysica acta 1985;806(1):1-8.
1985: H Dorkins; Claudine Junien; J L Mandel; Klaus Wrogemann; J P Moison; M Martinez; J M Old; S Bundey; M Schwartz; N Carpenter
Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy families.
Human genetics 1985;71(2):103-7.
1983: R G Thompson; B Nickel; S Finlayson; R Meuser; J L Hamerton; Klaus Wrogemann
56K fibroblast protein not specific for Duchenne muscular dystrophy but for skin biopsy site.
Nature 1983;304(5928):740-1.
1983: Edward Nylen; Klaus Wrogemann
Mitochondrial calcium content and oxidative phosphorylation in heart and skeletal muscle of dystrophic mice.
Experimental neurology 1983;80(1):69-80.
1982: R G Thompson; E S Sponder; E Rosenmann; J L Hamerton; Klaus Wrogemann
Proline incorporation by cultured skin fibroblasts from patients with duchenne muscular dystrophy.
Journal of the neurological sciences 1982;57(1):41-54.
1982: E Rosenmann; C Kreis; R G Thompson; M Dobbs; J L Hamerton; Klaus Wrogemann
Analysis of fibroblast proteins from patients with Duchenne muscular dystrophy by two-dimensional gel electrophoresis.
Nature 1982;298(5874):563-5.