Please enable Javascript

Labmeeting uses lots of Javascript - basically you can't use the site without it. So please enable Javascript in your browser. If your browser does not support Javascript, we recommend Firefox.

Papers authored by Schwarze U

Collect these papers and discover other ones on Labmeeting. Learn more.

Enhanced activity during associative encoding in the affected hippocampus in right temporal lobe epilepsy patients.

+ cite this

+ View Abstract

Schwarze U, Hahn C, Bengner T, Stodieck S, Büchel C, and Sommer T

Brain research 1297:112-7, 2009 Nov 10 - Who cited this? | PubMed ID: 19699186 | Fulltext

Successful Endovascular Repair of Acute Type B Aortic Dissection in Undiagnosed Ehlers-Danlos Syndrome Type IV.

+ cite this

+ View Abstract

Khalique Z, Lyons OT, Clough RE, Bell RE, Reidy JF, Schwarze U, Byers PH, and Taylor PR

European journal of vascular and endovascular surgery : the official journal of the European Society for Vascular Surgery 38(5):608-9, 2009 Nov - Who cited this? | PubMed ID: 19695909 | Fulltext

Molecular mechanisms of classical Ehlers-Danlos syndrome (EDS).

+ cite this

+ View Abstract

Mitchell AL, Schwarze U, Jennings JF, and Byers PH

Human mutation 30(6):995-1002, 2009 Jun - Who cited this? | PubMed ID: 19370768 | Fulltext

Mutation and polymorphism spectrum in osteogenesis imperfecta type II: implications for genotype-phenotype relationships.

+ cite this

+ View Abstract

Bodian DL, Chan TF, Poon A, Schwarze U, Yang K, Byers PH, Kwok PY, and Klein TE

Human molecular genetics 18(3):463-71, 2009 Feb 1 - Who cited this? | PubMed ID: 18996919 | Fulltext

CRTAP and LEPRE1 mutations in recessive osteogenesis imperfecta.

+ cite this

+ View Abstract

Baldridge D, Schwarze U, Morello R, Lennington J, Bertin TK, Pace JM, Pepin MG, Weis M, Eyre DR, Walsh J, Lambert D, Green A, Robinson H, Michelson M, Houge G, Lindman C,

(show remaining authors)

Human mutation, 2008 Jun 19 - Who cited this? | PubMed ID: 18566967 | Fulltext

Defective C-propeptides of the proalpha2(I) chain of type I procollagen impede molecular assembly and result in osteogenesis imperfecta.

+ cite this

+ View Abstract

Pace JM, Wiese M, Drenguis AS, Kuznetsova N, Leikin S, Schwarze U, Chen D, Mooney SH, Unger S, and Byers PH

The Journal of biological chemistry 283(23):16061, 2008 Jun 6 - Who cited this? | PubMed ID: 18375391 | Fulltext

MRI of great vessel morphology and function in Ehlers-Danlos syndrome type IV.

+ cite this

+ View Abstract

Kerwin W, Pepin M, Mitsumori L, Yarnykh V, Schwarze U, and Byers P

The international journal of cardiovascular imaging 24(5):519-28, 2008 Jun - Who cited this? | PubMed ID: 18043893 | Fulltext

Gene targeting of mutant COL1A2 alleles in mesenchymal stem cells from individuals with osteogenesis imperfecta.

+ cite this

+ View Abstract

Chamberlain JR, Deyle DR, Schwarze U, Wang P, Hirata RK, Li Y, Byers PH, and Russell DW

Molecular therapy : the journal of the American Society of Gene Therapy 16(1):187, 2008 Jan - Who cited this? | PubMed ID: 17955022 | Fulltext

Rapid aneurysmal degeneration of a Stanford type B aortic dissection in a patient with Loeys-Dietz syndrome.

+ cite this

Lee RS, Fazel S, Schwarze U, Fleischmann D, Berry GJ, Liang D, Miller DC, and Mitchell RS

The Journal of thoracic and cardiovascular surgery 134(1):242-3, 243.e1, 2007 Jul - Who cited this? | PubMed ID: 17599521 | Fulltext

Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycans.

+ cite this

+ View Abstract

Marini JC, Forlino A, Cabral WA, Barnes AM, San Antonio JD, Milgrom S, Hyland JC, Körkkö J, Prockop DJ, De Paepe A, Coucke P, Symoens S, Glorieux FH, Roughley PJ, Lund AM, Kuurila-Svahn K,

(show remaining authors)

Human mutation 28(3):209-21, 2007 Mar - Who cited this? | PubMed ID: 17078022 | Fulltext

CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta.

+ cite this

+ View Abstract

Morello R, Bertin TK, Chen Y, Hicks J, Tonachini L, Monticone M, Castagnola P, Rauch F, Glorieux FH, Vranka J, Bächinger HP, Pace JM, Schwarze U, Byers PH, Weis M, Fernandes RJ,

(show remaining authors)

Cell 127(2):291, 2006 Oct 20 - Who cited this? | PubMed ID: 17055431 | Fulltext

Aneurysm syndromes caused by mutations in the TGF-beta receptor.

+ cite this

+ View Abstract

Loeys BL, Schwarze U, Holm T, Callewaert BL, Thomas GH, Pannu H, De Backer JF, Oswald GL, Symoens S, Manouvrier S, Roberts AE, Faravelli F, Greco MA, Pyeritz RE, Milewicz DM, Coucke PJ,

(show remaining authors)

The New England journal of medicine 355(8):788-98, 2006 Aug 24 - Who cited this? | PubMed ID: 16928994 | Fulltext

Stability related bias in residues replacing glycines within the collagen triple helix (Gly-Xaa-Yaa) in inherited connective tissue disorders.

+ cite this

+ View Abstract

Persikov AV, Pillitteri RJ, Amin P, Schwarze U, Byers PH, and Brodsky B

Human mutation 24(4):330-7, 2004 Oct - Who cited this? | PubMed ID: 15365990 | Fulltext

Rare autosomal recessive cardiac valvular form of Ehlers-Danlos syndrome results from mutations in the COL1A2 gene that activate the nonsense-mediated RNA decay pathway.

+ cite this

+ View Abstract

Schwarze U, Hata R, McKusick VA, Shinkai H, Hoyme HE, Pyeritz RE, and Byers PH

American journal of human genetics 74(5):917-30, 2004 May - Who cited this? | PubMed ID: 15077201 | Fulltext

Gene targeting in stem cells from individuals with osteogenesis imperfecta.

+ cite this

+ View Abstract

Chamberlain JR, Schwarze U, Wang PR, Hirata RK, Hankenson KD, Pace JM, Underwood RA, Song KM, Sussman M, Byers PH, and Russell DW

Science (New York, N.Y.) 303(5661):1198-201, 2004 Feb 20 - Who cited this? | PubMed ID: 14976317 | Fulltext

Neurological presentation of Ehlers-Danlos syndrome type IV in a family with parental mosaicism.

+ cite this

+ View Abstract

Palmeri S, Mari F, Meloni I, Malandrini A, Ariani F, Villanova M, Pompilio A, Schwarze U, Byers PH, and Renieri A

Clinical genetics 63(6):510-5, 2003 Jun - Who cited this? | PubMed ID: 12786757 | Fulltext

Order of intron removal influences multiple splice outcomes, including a two-exon skip, in a COL5A1 acceptor-site mutation that results in abnormal pro-alpha1(V) N-propeptides and Ehlers-Danlos syndrome type I.

+ cite this

+ View Abstract

Takahara K, Schwarze U, Imamura Y, Hoffman GG, Toriello H, Smith LT, Byers PH, and Greenspan DS

American journal of human genetics 71(3):451, 2002 Sep - Who cited this? | PubMed ID: 12145749 | Fulltext

Ehlers-Danlos syndrome type IV and a novel mutation of the type III procollagen gene as a cause of abdominal apoplexy.

+ cite this

+ View Abstract

Hassan I, Rasmussen TE, Schwarze U, Rose PS, Whiteman DA, and Gloviczki P

Mayo Clinic proceedings. Mayo Clinic 77(8):861-3, 2002 Aug - Who cited this? | PubMed ID: 12173720 | Fulltext

Spontaneous direct carotid-cavernous fistula in Ehlers-Danlos syndrome type IV: two case reports and a review of the literature.

+ cite this

+ View Abstract

Chuman H, Trobe JD, Petty EM, Schwarze U, Pepin M, Byers PH, and Deveikis JP

Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society 22(2):75-81, 2002 Jun - Who cited this? | PubMed ID: 12131463 | Fulltext

A single amino acid substitution (D1441Y) in the carboxyl-terminal propeptide of the proalpha1(I) chain of type I collagen results in a lethal variant of osteogenesis imperfecta with features of dense bone diseases.

+ cite this

+ View Abstract

Pace JM, Chitayat D, Atkinson M, Wilcox WR, Schwarze U, and Byers PH

Journal of medical genetics 39(1):23-9, 2002 Jan - Who cited this? | PubMed ID: 11826020 | Fulltext

Haploinsufficiency for one COL3A1 allele of type III procollagen results in a phenotype similar to the vascular form of Ehlers-Danlos syndrome, Ehlers-Danlos syndrome type IV.

+ cite this

+ View Abstract

Schwarze U, Schievink WI, Petty E, Jaff MR, Babovic-Vuksanovic D, Cherry KJ, Pepin M, and Byers PH

American journal of human genetics 69(5):989-1001, 2001 Nov - Who cited this? | PubMed ID: 11577371 | Fulltext

Cyclosporin A and therapeutic plasma exchange in the treatment of severe systemic lupus erythematosus.

+ cite this

+ View Abstract

Bambauer R, Schwarze U, and Schiel R

Artificial organs 24(11):852-6, 2000 Nov - Who cited this? | PubMed ID: 11119071 | Fulltext

Null alleles of the COL5A1 gene of type V collagen are a cause of the classical forms of Ehlers-Danlos syndrome (types I and II).

+ cite this

+ View Abstract

Schwarze U, Atkinson M, Hoffman GG, Greenspan DS, and Byers PH

American journal of human genetics 66(6):1757-65, 2000 Jun - Who cited this? | PubMed ID: 10796876 | Fulltext

Clinical and genetic features of Ehlers-Danlos syndrome type IV, the vascular type.

+ cite this

+ View Abstract

Pepin M, Schwarze U, Superti-Furga A, and Byers PH

The New England journal of medicine 342(10):673-80, 2000 Mar 9 - Who cited this? | PubMed ID: 10706896 | Fulltext

Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase gene.

+ cite this

+ View Abstract

Colige A, Sieron AL, Li SW, Schwarze U, Petty E, Wertelecki W, Wilcox W, Krakow D, Cohn DH, Reardon W, Byers PH, Lapière CM, Prockop DJ, and Nusgens BV

American journal of human genetics 65(2):308-17, 1999 Aug - Who cited this? | PubMed ID: 10417273 | Fulltext

Redefinition of exon 7 in the COL1A1 gene of type I collagen by an intron 8 splice-donor-site mutation in a form of osteogenesis imperfecta: influence of intron splice order on outcome of splice-site mutation.

+ cite this

+ View Abstract

Schwarze U, Starman BJ, and Byers PH

American journal of human genetics 65(2):336-44, 1999 Aug - Who cited this? | PubMed ID: 10417276 | Fulltext

Large kindred with Ehlers-Danlos syndrome type IV due to a point mutation (G571S) in the COL3A1 gene of type III procollagen: low risk of pregnancy complications and unexpected longevity in some affected relatives.

+ cite this

+ View Abstract

Gilchrist D, Schwarze U, Shields K, MacLaren L, Bridge PJ, and Byers PH

American journal of medical genetics 82(4):305-11, 1999 Feb 12 - Who cited this? | PubMed ID: 10051163 | Fulltext

Multiple vascular and bowel ruptures in an adolescent male with sporadic Ehlers-Danlos syndrome type IV.

+ cite this

+ View Abstract

Collins MH, Schwarze U, Carpentieri DF, Kaplan P, Nathanson K, Meyer JS, and Byers PH

Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society 2(1):86-93, 1999 - Who cited this? | PubMed ID: 9841712 | Fulltext

Splicing defects in the COL3A1 gene: marked preference for 5' (donor) spice-site mutations in patients with exon-skipping mutations and Ehlers-Danlos syndrome type IV.

+ cite this

+ View Abstract

Schwarze U, Goldstein JA, and Byers PH

American journal of human genetics 61(6):1276-86, 1997 Dec - Who cited this? | PubMed ID: 9399899 | Fulltext

Ehlers-Danlos syndrome type VIIA and VIIB result from splice-junction mutations or genomic deletions that involve exon 6 in the COL1A1 and COL1A2 genes of type I collagen.

+ cite this

+ View Abstract

Byers PH, Duvic M, Atkinson M, Robinow M, Smith LT, Krane SM, Greally MT, Ludman M, Matalon R, Pauker S, Quanbeck D, and Schwarze U

American journal of medical genetics 72(1):94-105, 1997 Oct 3 - Who cited this? | PubMed ID: 9295084 | Fulltext

Mutations in the COL3A1 gene result in the Ehlers-Danlos syndrome type IV and alterations in the size and distribution of the major collagen fibrils of the dermis.

+ cite this

+ View Abstract

Smith LT, Schwarze U, Goldstein J, and Byers PH

The Journal of investigative dermatology 108(3):241-7, 1997 Mar - Who cited this? | PubMed ID: 9036918 | Fulltext

The deletion of six amino acids at the C-terminus of the alpha 1 (II) chain causes overmodification of type II and type XI collagen: further evidence for the association between small deletions in COL2A1 and Kniest dysplasia.

+ cite this

+ View Abstract

Winterpacht A, Superti-Furga A, Schwarze U, Stöss H, Steinmann B, Spranger J, and Zabel B

Journal of medical genetics 33(8):649-54, 1996 Aug - Who cited this? | PubMed ID: 8863156 | Fulltext

Non-radioactive multiplex-SSCP analysis: detection of a new type II procollagen gene (COL2A1) mutation.

+ cite this

+ View Abstract

Winterpacht A, Hilbert K, Schwarze U, and Zabel B

Human genetics 95(4):437-9, 1995 Apr - Who cited this? | PubMed ID: 7705841 | Fulltext

Alternative splicing as the result of a type II procollagen gene (COL2A1) mutation in a patient with Kniest dysplasia.

+ cite this

Winterpacht A, Schwarze U, Mundlos S, Menger H, Spranger J, and Zabel B

Human molecular genetics 3(10):1891-3, 1994 Oct - Who cited this? | PubMed ID: 7849719 | Fulltext

Autosomal dominant spondylarthropathy due to a type II procollagen gene (COL2A1) point mutation.

+ cite this

+ View Abstract

Winterpacht A, Hilbert M, Schwarze U, Mundlos S, Spranger J, and Zabel B

Human mutation 4(4):257-62, 1994 - Who cited this? | PubMed ID: 7866404 | Fulltext

Kniest and Stickler dysplasia phenotypes caused by collagen type II gene (COL2A1) defect.

+ cite this

+ View Abstract

Winterpacht A, Hilbert M, Schwarze U, Mundlos S, Spranger J, and Zabel BU

Nature genetics 3(4):323-6, 1993 Apr - Who cited this? | PubMed ID: 7981752 | Fulltext

[Clinical importance of hepatitis B virus DNA detection in serum of children with chronic hepatitis B].

+ cite this

+ View Abstract

Wirth S, Möllers U, Schaefer E, Schwarze U, and Zabel B

Klinische Padiatrie 204(3):155-7, 1992 - Who cited this? | PubMed ID: 1614181 | Fulltext

[Retinoschisis with a giant central outer layer retinal tear and concomitant detachment].

+ cite this

+ View Abstract

Schwarze U and Laqua H

Klinische Monatsblatter fur Augenheilkunde 197(1):50-2, 1990 Jul - Who cited this? | PubMed ID: 2395302 | Fulltext

Bioassay for determination of nystatin in faeces after oral application.

+ cite this

+ View Abstract

Blaschke-Hellmessen R and Schwarze U

Mycoses 33(3):129-35, 1990 Mar - Who cited this? | PubMed ID: 2113608 | Fulltext

[Temporal arteritis with hypotension syndrome and necrosis of the scalp].

+ cite this

+ View Abstract

Schwarze U and Lautier R

Klinische Monatsblatter fur Augenheilkunde 190(3):188-91, 1987 Mar - Who cited this? | PubMed ID: 3586538 | Fulltext

Search Google Scholar for Schwarze U

Join Labmeeting

Organize and search your PDF collection
Collect papers
Search millions of papers
Keep up to date with paper alerts
Read your papers from anywhere
Recommend papers to colleagues
Manage your lab

Labmeeting is a web service for researchers. Sign up with your academic email address.

Individuals or corporations not affiliated with an academic institution can request a trial subscription.

Got a question?
The Labmeeting Network
has the answer.
Ask scientists at top universities like Harvard, Stanford, and MIT for their expert opinion!