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Jochen Graw

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Kristina Bannik; Claudia Dalke; Theresa Faus-Kessler; Maria Gomolka; Sabine Hornhardt; Olena Klymenko; Ulrike Kulka; Michael Rosemann; Ute Rössler; Klaus-Rüdiger Trott; Michael Atkinson; Jochen Graw
Are mouse lens epithelial cells more sensitive to γ-irradiation than lymphocytes?
Simone Renner; Elisabeth Streckel; Rüdiger Wanke; Annegret Wünsch; Andrea Bähr; Helmut Blum; Andreas Blutke; Christina Braun-Reichhart; Daniela Emrich; Jochen Graw; Nadja Herbach; Barbara Kessler; Annegret Wuensch; Stefan Krebs; Mayuko Kurome; Hiroshi Nagashima; Oliver Puk; Eckhard Wolf
Permanent neonatal diabetes in INSC94Y transgenic pigs.
Misu Lee; Federico Roncaroli; Marily Theodoropoulou; Maria Chiara Zatelli; Jochen Graw; Natalia S Pellegata
Levels of p27 sensitize to dual PI3K/mTOR inhibition.

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All Publications

2013: Kristina Bannik; Claudia Dalke; Theresa Faus-Kessler; Maria Gomolka; Sabine Hornhardt; Olena Klymenko; Ulrike Kulka; Michael Rosemann; Ute Rössler; Klaus-Rüdiger Trott; Michael Atkinson; Jochen Graw
Are mouse lens epithelial cells more sensitive to γ-irradiation than lymphocytes?
Radiation and environmental biophysics 2013;52(2):279-86.
2013: Simone Renner; Elisabeth Streckel; Rüdiger Wanke; Annegret Wünsch; Andrea Bähr; Helmut Blum; Andreas Blutke; Christina Braun-Reichhart; Daniela Emrich; Jochen Graw; Nadja Herbach; Barbara Kessler; Annegret Wuensch; Stefan Krebs; Mayuko Kurome; Hiroshi Nagashima; Oliver Puk; Eckhard Wolf
Permanent neonatal diabetes in INSC94Y transgenic pigs.
Diabetes 2013;62(5):1505-11.
2011: Misu Lee; Federico Roncaroli; Marily Theodoropoulou; Maria Chiara Zatelli; Jochen Graw; Natalia S Pellegata
Levels of p27 sensitize to dual PI3K/mTOR inhibition.
Molecular cancer therapeutics 2011;10(8):1450-9.
2011: Oliver Puk; Sibylle Wagner; Kathrin Krowiorz; Gabriele Möller; Jerzy Adamski; Nafees Ahmad; Martin Hrabé De Angelis; Arie Geerlof; Jochen Graw
The pathologic effect of a novel neomorphic Fgf9(Y162C) allele is restricted to decreased vision and retarded lens growth.
PloS one 2011;6(8):e23678.
2010: Alena Shyla; Gabriele Hölzlwimmer; Julia Calzada-Wack; Karin Bink; Oleg Tischenko; Marie-Noëlle Guilly; Sylvie Chevillard; Elenore Samson; Jochen Graw; Michael J Atkinson; Natalia S Pellegata
Allelic loss of chromosomes 8 and 19 in MENX-associated rat pheochromocytoma.
International journal of cancer. Journal international du cancer 2010;126(10):2362-72.
2010: Sathiyavedu T Santhiya; Ganesan Senthil Kumar; Pridhvi Sudhakar; Navnit Gupta; Norman Klopp; Thomas Illig; Torben Söker; Marco Groth; Matthias Platzer; Puthiya M Gopinath; Jochen Graw
Molecular analysis of cataract families in India: new mutations in the CRYBB2 and GJA3 genes and rare polymorphisms.
Molecular vision 2010;16():1837-47.
2009: Oliver Puk; Irene Esposito; Torben Söker; Jana Löster; Birgit Budde; Peter Nürnberg; Dian Michel-Soewarto; Helmut Fuchs; Eckhard Wolf; Martin Hrabé De Angelis; Jochen Graw
A new Fgf10 mutation in the mouse leads to atrophy of the harderian gland and slit-eye phenotype in heterozygotes: a novel model for dry-eye disease?
Investigative ophthalmology & visual science 2009;50(9):4311-8.
2008: Koustav Ganguly; Jack Favor; Angelika Neuhäuser-Klaus; Rodica Sandulache; Oliver Puk; Johannes Beckers; Marion Horsch; Sandra Schädler; Daniela Vogt Weisenhorn; Wolfgang Wurst; Jochen Graw
Novel allele of crybb2 in the mouse and its expression in the brain.
Investigative ophthalmology & visual science 2008;49(4):1533-41.
2008: Oliver Puk; Jana Löster; Claudia Dalke; Dian Soewarto; Helmut Fuchs; Birgit Budde; Peter Nürnberg; Eckhard Wolf; Martin Hrabé De Angelis; Jochen Graw
Mutation in a novel connexin-like gene (Gjf1) in the mouse affects early lens development and causes a variable small-eye phenotype.
Investigative ophthalmology & visual science 2008;49(4):1525-32.
2008: Oliver Puk; Claudia Dalke; Martin Hrabé de Angelis; Jochen Graw
Variation of the response to the optokinetic drum among various strains of mice.
Frontiers in bioscience : a journal and virtual library 2008;13():6269-75.
2007: Silke Pauli; Torben Söker; Norman Klopp; Thomas Illig; Wolfgang Engel; Jochen Graw
Mutation analysis in a German family identified a new cataract-causing allele in the CRYBB2 gene.
Molecular vision 2007;13():962-7.
2006: Natalia S Pellegata; Leticia Quintanilla-Martinez; Heide Siggelkow; Elenore Samson; Karin Bink; Heinz Höfler; Falko Fend; Jochen Graw; Michael J Atkinson
Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans.
Proceedings of the National Academy of Sciences of the United States of America 2006;103(42):15558-63.
2006: Gail Billingsley; Sathiyavedu T Santhiya; Andrew D Paterson; Koji Ogata; Shoshana J Wodak; S Mohsen Hosseini; Shyam Manohar Manisastry; Perumalsamy Vijayalakshmi; Puthiya M Gopinath; Jochen Graw; Elise Héon
CRYBA4, a novel human cataract gene, is also involved in microphthalmia.
American journal of human genetics 2006;79(4):702-9.
2006: Oliver Puk; Claudia Dalke; Jack Favor; Martin Hrabé De Angelis; Jochen Graw
Variations of eye size parameters among different strains of mice.
Mammalian genome : official journal of the International Mammalian Genome Society 2006;17(8):851-7.
2006: Jochen Graw; Norman Klopp; Thomas Illig; Markus N Preising; Birgit Lorenz
Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in P.
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie 2006;244(8):912-9.
2006: E Berber; I D Fidanci; C Un; Osman El-Maarri; Gülten Aktuglu; A Gurgey; Tiraje Celkan; Adalet Meral; J Oldenburg; Jochen Graw; N Akar; H Caglayan
Sequencing of the factor 8(F8) coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations, and one rediagnosis of von Willebrand's disease type 2N.
Haemophilia : the official journal of the World Federation of Hemophilia 2006;12(4):398-400.
2006: Osman El-Maarri; Heike Singer; Claudia Klein; Matthias Watzka; Ursula Herbiniaux; Hans H Brackmann; Jörg Schröder; Jochen Graw; Clemens R Müller; Wolfgang Schramm; Rainer Schwaab; Thomas Haaf; Peter Hanfland; Johannes Oldenburg
Lack of F8 mRNA: a novel mechanism leading to hemophilia A.
Blood 2006;107(7):2759-65.
2006: Sathiyavedu T Santhiya; Torben Soker; Norman Klopp; Thomas Illig; M V S Prakash; Bhavani Selvaraj; Puthiya M Gopinath; Jochen Graw
Identification of a novel, putative cataract-causing allele in CRYAA (G98R) in an Indian family.
Molecular vision 2006;12():768-73.
2005: Jochen Graw; Jana Löster; Oliver Puk; Doris Münster; Nicole Haubst; Dian Soewarto; Helmut Fuchs; Birgit Meyer; Peter Nürnberg; Walter Pretsch; Paul Selby; Jack Favor; Eckhard Wolf; Martin Hrabé De Angelis
Three novel Pax6 alleles in the mouse leading to the same small-eye phenotype caused by different consequences at target promoters.
Investigative ophthalmology & visual science 2005;46(12):4671-83.
2005: Marlon R Schneider; Maik Dahlhoff; Nadja Herbach; Ingrid Renner-Mueller; Claudia Dalke; Oliver Puk; Jochen Graw; Rüdiger Wanke; Eckhard Wolf
Betacellulin overexpression in transgenic mice causes disproportionate growth, pulmonary hemorrhage syndrome, and complex eye pathology.
Endocrinology 2005;146(12):5237-46.
2005: Johannes Lengler; Tobias Bittner; Doris Münster; Alaa El-Din A Gawad; Jochen Graw
Agonistic and antagonistic action of AP2, Msx2, Pax6, Prox1 AND Six3 in the regulation of Sox2 expression.
Ophthalmic research 2005;37(6):301-9.
2005: Claudia Dalke; Jochen Graw
Mouse mutants as models for congenital retinal disorders.
Experimental eye research 2005;81(5):503-12.
2005: Jochen Graw; Hans H Brackmann; Johannes Oldenburg; Reinhard Schneppenheim; Michael Spannagl; Rainer Schwaab
Haemophilia A: from mutation analysis to new therapies.
Nature reviews. Genetics 2005;6(6):488-501.
2005: Claudia Dalke; Uwe Pleyer; Jochen Graw
On the use of Tono-Pen XL for the measurement of intraocular pressure in mice.
Experimental eye research 2005;80(2):295-6.
2005: Osman El-Maarri; Ursula Herbiniaux; Jochen Graw; J Schröder; A Terzic; Matthias Watzka; Hans H Brackmann; W Schramm; Peter Hanfland; Rainer Schwaab; Clemens R Müller; Johannes Oldenburg
Analysis of mRNA in hemophilia A patients with undetectable mutations reveals normal splicing in the factor VIII gene.
Journal of thrombosis and haemostasis : JTH 2005;3(2):332-9.
2005: Monica M Jablonski; Claudia Dalke; XiaoFei Wang; Lu Lu; Kenneth F Manly; Walter Pretsch; Jack Favor; Machelle T Pardue; Eugene M Rinchik; Robert Williams; Dan Goldowitz; Jochen Graw
An ENU-induced mutation in Rs1h causes disruption of retinal structure and function.
Molecular vision 2005;11():569-81.
2004: Nicole Haubst; Joachim Berger; Venugopal Radjendirane; Jochen Graw; Jack Favor; Grady F Saunders; Anastassia Stoykova; Magdalena Götz
Molecular dissection of Pax6 function: the specific roles of the paired domain and homeodomain in brain development.
Development (Cambridge, England) 2004;131(24):6131-40.
2004: Sathiyavedu T Santhiya; Shyam Manohar Manisastry; Deepika Rawlley; Raghunathan Malathi; Sharmila Anishetty; Puthiya M Gopinath; Perumalsamy Vijayalakshmi; Perumalsamy Namperumalsamy; Jerzy Adamski; Jochen Graw
Mutation analysis of congenital cataracts in Indian families: identification of SNPS and a new causative allele in CRYBB2 gene.
Investigative ophthalmology & visual science 2004;45(10):3599-607.
2004: Jochen Graw; Angelika Neuhäuser-Klaus; Norman Klopp; Paul B Selby; Jana Löster; Jack Favor
Genetic and allelic heterogeneity of Cryg mutations in eight distinct forms of dominant cataract in the mouse.
Investigative ophthalmology & visual science 2004;45(4):1202-13.
2004: Kamilla Piotrowska; Natalia S Pellegata; Michael Rosemann; Andreas Fritz; Jochen Graw; Michael J Atkinson
Mapping of a novel MEN-like syndrome locus to rat chromosome 4.
Mammalian genome : official journal of the International Mammalian Genome Society 2004;15(2):135-41.
2004: Claudia Dalke; Jana Löster; Helmut Fuchs; Valérie Gailus-Durner; Dian Soewarto; Jack Favor; Angelika Neuhäuser-Klaus; Walter Pretsch; Florian Gekeler; Kei Shinoda; Eberhart Zrenner; Thomas Meitinger; Martin Hrabé De Angelis; Jochen Graw
Electroretinography as a screening method for mutations causing retinal dysfunction in mice.
Investigative ophthalmology & visual science 2004;45(2):601-9.
2004: Jochen Graw
Congenital hereditary cataracts.
The International journal of developmental biology 2004;48(8-9):1031-44.
2003: Jochen Graw
The genetic and molecular basis of congenital eye defects.
Nature reviews. Genetics 2003;4(11):876-88.
2003: Jochen Graw; Walter Pretsch; Jana Löster
Mutation in intron 6 of the hamster Mitf gene leads to skipping of the subsequent exon and creates a novel animal model for the human Waardenburg syndrome type II.
Genetics 2003;164(3):1035-41.
2003: Jochen Graw; Jana Löster
Developmental genetics in ophthalmology.
Ophthalmic genetics 2003;24(1):1-33.
2003: Norman Klopp; Elise Héon; Gail Billingsley; Thomas Illig; Matthias Wjst; Günther Rudolph; Jochen Graw
Further genetic heterogeneity for autosomal dominant human sutural cataracts.
Ophthalmic research 2003;35(2):71-7.
2003: Hans H Brackmann; Thilo Albert; Jochen Graw; Johannes Oldenburg; W Schramm; Rainer Schwaab
[Gathering and evaluation of phenotype data of haemophilia A patients for correlation with genotype data].
Hämostaseologie 2003;23(1):24-7.
2003: H Krebs; C Domsch; K Adelhard; Hans H Brackmann; Jochen Graw; J Oldenburg; Rainer Schwaab; W Schramm
[The national GTH haemophilia registry as database within the scope of the German human genome project].
Hämostaseologie 2003;23(1):18-23.
2003: Thilo Albert; S Lange; Johannes Oldenburg; Jochen Graw; W Schramm; Peter Hanfland; Hans H Brackmann; Rainer Schwaab
[Characterization of factor VIII antibody epitopes from haemophilia A patients using cellulose bound FVIII peptide libraries].
Hämostaseologie 2003;23(1):13-7.
2003: Johannes Oldenburg; J Schröder; Jochen Graw; Vytautas Ivaskevicius; Hans H Brackmann; W Schramm; Clemens R Müller; Erhard Seifried; Rainer Schwaab
[Significance of mutation analysis in patients with haemophilia A].
Hämostaseologie 2003;23(1):6-12.
2003: C Uen; J Oldenburg; J Schröder; H-J Brackmann; W Schramm; Rainer Schwaab; R Schneppenheim; Jochen Graw
[2% Haemophilia A patients without mutation in the FVIII gene].
Hämostaseologie 2003;23(1):1-5.
2003: Barbara Angeletti; Jana Löster; Alberto Auricchio; Florian Gekeler; Kei Shinoda; Andrea Ballabio; Jochen Graw; Valeria Marigo
An in vivo doxycycline-controlled expression system for functional studies of the retina.
Investigative ophthalmology & visual science 2003;44(2):755-60.
2002: Aileen Sandilands; Aileen M Hutcheson; Heather A Long; Alan R Prescott; Gijs Vrensen; Jana Löster; Norman Klopp; Raimund B Lutz; Jochen Graw; Shigeo Masaki; Christopher M Dobson; Cait E MacPhee; Roy A Quinlan
Altered aggregation properties of mutant gamma-crystallins cause inherited cataract.
The EMBO journal 2002;21(22):6005-14.
2002: Jochen Graw; Norman Klopp; Angelika Neuhäuser-Klaus; Jack Favor; Jana Löster
Crygf(Rop): the first mutation in the Crygf gene causing a unique radial lens opacity.
Investigative ophthalmology & visual science 2002;43(9):2998-3002.
2002: Jochen Graw; Jana Löster; Dian Soewarto; Helmut Fuchs; André Reis; Eckhard Wolf; Rudi Balling; Martin Hrabé De Angelis
V76D mutation in a conserved gD-crystallin region leads to dominant cataracts in mice.
Mammalian genome : official journal of the International Mammalian Genome Society 2002;13(8):452-5.
2002: Jochen Graw; Angelika Neuhäuser-Klaus; Jana Löster; Norman Klopp; Jack Favor
Ethylnitrosourea-induced base pair substitution affects splicing of the mouse gammaE-crystallin encoding gene leading to the expression of a hybrid protein and to a cataract.
Genetics 2002;161(4):1633-40.
2002: N Klopp; J Oldenburg; C Uen; R Schneppenheim; Jochen Graw
11 hemophilia A patients without mutations in the factor VIII encoding gene.
Thrombosis and haemostasis 2002;88(2):357-60.
2002: Guy Goudreau; Petros Petrou; Lixing W Reneker; Jochen Graw; Jana Löster; Peter Gruss
Mutually regulated expression of Pax6 and Six3 and its implications for the Pax6 haploinsufficient lens phenotype.
Proceedings of the National Academy of Sciences of the United States of America 2002;99(13):8719-24.
2002: Andreas Fritz; Axel Walch; Kamilla Piotrowska; Michael Rosemann; Ekkehard Schäffer; Karin Weber; Andreas Timper; Gerhild Wildner; Jochen Graw; Heinz Höfler; Michael J Atkinson
Recessive transmission of a multiple endocrine neoplasia syndrome in the rat.
Cancer research 2002;62(11):3048-51.
2002: Sathiyavedu T Santhiya; M Shyam Manohar; D Rawlley; P Vijayalakshmi; Perumalsamy Namperumalsamy; Puthiya M Gopinath; Jana Löster; Jochen Graw
Novel mutations in the gamma-crystallin genes cause autosomal dominant congenital cataracts.
Journal of medical genetics 2002;39(5):352-8.
2002: Jochen Graw; Angelika Neuhäuser-Klaus; Jana Löster; Jack Favor
A 6-bp deletion in the Crygc gene leading to a nuclear and radial cataract in the mouse.
Investigative ophthalmology & visual science 2002;43(1):236-40.
2001: Jochen Graw; Jana Löster; Dian Soewarto; Helmut Fuchs; Birgit Meyer; André Reis; Eckhard Wolf; Rudi Balling; Martin Hrabé De Angelis
Characterization of a mutation in the lens-specific MP70 encoding gene of the mouse leading to a dominant cataract.
Experimental eye research 2001;73(6):867-76.
2001: Jochen Graw; Jana Löster; Dian Soewarto; Helmut Fuchs; Birgit Meyer; André Reis; Eckhard Wolf; Rudi Balling; Martin Hrabé De Angelis
Characterization of a new, dominant V124E mutation in the mouse alphaA-crystallin-encoding gene.
Investigative ophthalmology & visual science 2001;42(12):2909-15.
2001: Johannes Lengler; Jochen Graw
Regulation of the human SIX3 gene promoter.
Biochemical and biophysical research communications 2001;287(2):372-6.
2001: Jochen Graw; Jana Löster; Dian Soewarto; Helmut Fuchs; A Reis; E Wolf; Rudi Balling; Martin Hrabé De Angelis
Aey2, a new mutation in the betaB2-crystallin-encoding gene of the mouse.
Investigative ophthalmology & visual science 2001;42(7):1574-80.
2001: Jochen Graw; Norman Klopp; Jana Löster; Dian Soewarto; Helmut Fuchs; J Becker-Follmann; André Reis; Eckhard Wolf; Rudi Balling; M Habré de Angelis
Ethylnitrosourea-induced mutation in mice leads to the expression of a novel protein in the eye and to dominant cataracts.
Genetics 2001;157(3):1313-20.
2001: Johannes Lengler; E Krausz; S Tomarev; Alan R Prescott; Roy A Quinlan; Jochen Graw
Antagonistic action of Six3 and Prox1 at the gamma-crystallin promoter.
Nucleic acids research 2001;29(2):515-26.
2001: Norman Klopp; Jana Löster; Jochen Graw
Characterization of a 1-bp deletion in the gammaE-crystallin gene leading to a nuclear and zonular cataract in the mouse.
Investigative ophthalmology & visual science 2001;42(1):183-7.
1999: Jochen Graw; M Jung; Jana Löster; Norman Klopp; Dian Soewarto; C Fella; Helmut Fuchs; André Reis; Eckhard Wolf; Rudi Balling; Martin Hrabé De Angelis
Mutation in the betaA3/A1-crystallin encoding gene Cryba1 causes a dominant cataract in the mouse.
Genomics 1999;62(1):67-73.
1999: Jochen Graw
Mouse models of congenital cataract.
Eye (London, England) 1999;13 ( Pt 3b)():438-44.
1999: Jochen Graw
Cataract mutations and lens development.
Progress in retinal and eye research 1999;18(2):235-67.
1998: Norman Klopp; Jack Favor; Jana Löster; Raimund B Lutz; Angelika Neuhäuser-Klaus; Alan R Prescott; Walter Pretsch; Roy A Quinlan; Aileen Sandilands; G F Vrensen; Jochen Graw
Three murine cataract mutants (Cat2) are defective in different gamma-crystallin genes.
Genomics 1998;52(2):152-8.
1998: C Grimm; B Chatterjee; Jack Favor; T Immervoll; Jana Löster; Norman Klopp; R Sandulache; Jochen Graw
Aphakia (ak), a mouse mutation affecting early eye development: fine mapping, consideration of candidate genes and altered Pax6 and Six3 gene expression pattern.
Developmental genetics 1998;23(4):299-316.
1998: T Immervoll; J Adamski; Jochen Graw
Polymorphism in the murine Tr2-11 gene encoding an orphan receptor, and its exclusion as a candidate gene for the cataract mutation Cat3.
Biological chemistry 1998;379(1):83-5.
1997: Jana Löster; T Immervoll; Thomas Schmitt-John; Jochen Graw
Cat3vl and Cat3vao cataract mutations on mouse chromosome 10: phenotypic characterization, linkage studies and analysis of candidate genes.
Molecular & general genetics : MGG 1997;257(1):97-102.
1997: Jochen Graw
The crystallins: genes, proteins and diseases.
Biological chemistry 1997;378(11):1331-48.
1997: D Pietrowski; Jochen Graw
Autokinase activity of alpha-crystallin inhibits its specific interaction with the DOTIS element in the murine gamma D/E/F-crystallin promoter in vitro.
Biological chemistry 1997;378(10):1183-6.
1997: Jochen Graw; Angelika Neuhäuser-Klaus; Walter Pretsch
Detection of a point mutation (A to G) in exon 5 of the murine Mgf gene defines a novel allele at the Steel locus with a weak phenotype.
Mutation research 1997;382(1-2):75-8.
1997: C Forker; Alfred Wegener; Jochen Graw
Effects of UV-B radiation on a hereditary suture cataract in mice.
Experimental eye research 1997;64(3):405-11.
1997: Tobias Stoeger; R C Augusteyn; Jochen Graw
The Cryner element in the murine gamma-crystallin promoters interacts with lens proteins.
Ophthalmic research 1997;29(3):161-71.
1996: Jochen Graw; Jana Löster; Angelika Neuhäuser-Klaus; Walter Pretsch; T Schmitt-John
Molecular analysis of two new Steel mutations in mice shows a transversion or an insertion.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(11):843-6.
1996: E Krausz; Jochen Graw
A new cat reporter gene vector designed for rapid and efficient cloning of PCR products.
Gene 1996;177(1-2):99-102.
1996: Konstantinos Zarbalis; B Chatterjee; Jana Löster; Thomas Werner; Jochen Graw
Sequence analysis of the beta B2-crystallin cDNA of hamster containing a domain conserved among vertebrates.
Gene 1996;174(1):181-4.
1996: E Krausz; R C Augusteyn; R A Quinlan; John R Reddan; P Russell; C M Sax; Jochen Graw
Expression of Crystallins, Pax6, Filensin, CP49, MIP, and MP20 in lens-derived cell lines.
Investigative ophthalmology & visual science 1996;37(10):2120-8.
1996: Jochen Graw
Genetic aspects of embryonic eye development in vertebrates.
Developmental genetics 1996;18(3):181-97.
1995: S T Santhiya; S M Abd-alla; Jana Löster; Jochen Graw
Reduced levels of gamma-crystallin transcripts during embryonic development of murine Cat2nop mutant lenses.
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie 1995;233(12):795-800.
1995: Jochen Graw; V Erfle
[Virus-free preparations of factor VIII].
Deutsche medizinische Wochenschrift (1946) 1995;120(7):221-4.
1994: R Sandulache; Walter Pretsch; B Chatterjee; W Gimbel; Jochen Graw; Jack Favor
Molecular analysis of four lactate dehydrogenase-A mutants in the mouse.
Mammalian genome : official journal of the International Mammalian Genome Society 1994;5(12):777-80.
1994: Jana Löster; Walter Pretsch; R Sandulache; T Schmitt-John; M F Lyon; Jochen Graw
Close linkage of the dominant cataract mutations (Cat-2) with Idh-1 and cryge on mouse chromosome 1.
Genomics 1994;23(1):240-2.
1994: D Pietrowski; M J Durante; A Liebstein; T Schmitt-John; Thomas Werner; Jochen Graw
Alpha-crystallins are involved in specific interactions with the murine gamma D/E/F-crystallin-encoding gene.
Gene 1994;144(2):171-8.
1993: Jochen Graw; A Liebstein; D Pietrowski; T Schmitt-John; Thomas Werner
Genomic sequences of murine gamma B- and gamma C-crystallin-encoding genes: promoter analysis and complete evolutionary pattern of mouse, rat and human gamma-crystallins.
Gene 1993;136(1-2):145-56.
1993: Jochen Graw; A Liebstein
DNase activity in murine lenses: implications for cataractogenesis.
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie 1993;231(6):354-8.
1992: S Merkle; Jack Favor; Jochen Graw; S Hornhardt; Walter Pretsch
Hereditary lactate dehydrogenase A-subunit deficiency as cause of early postimplantation death of homozygotes in Mus musculus.
Genetics 1992;131(2):413-21.
1991: Jochen Graw; L Coban; A Liebstein; Thomas Werner
Murine gamma E-crystallin is distinct from murine gamma 2-crystallin.
Gene 1991;104(2):265-70.
1990: Jochen Graw; W Bors; P M Gopinath; S Merkle; C Michel; Peter Reitmeir; E Schäffer; K H Summer; A Wulff
Characterization of Cat-2t, a radiation-induced dominant cataract mutation in mice.
Investigative ophthalmology & visual science 1990;31(7):1353-61.
1990: Jochen Graw; Thomas Werner; S Merkle; Peter Reitmeir; E Schäffer; A Wulff
Histological and biochemical characterization of the murine cataract mutant Nop.
Experimental eye research 1990;50(5):449-56.
1990: Jochen Graw; Peter Reitmeir; A Wulff
Osmotic state of lenses in three dominant murine cataract mutants.
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie 1990;228(3):252-4.
1989: Jochen Graw; J Kratochvilova; A Löbke; Peter Reitmeir; E Schäffer; A Wulff
Characterization of Scat (suture cataract), a dominant cataract mutation in mice.
Experimental eye research 1989;49(3):469-77.
1989: Jochen Graw; W Bors; C Michel; Peter Reitmeir; K H Summer; A Wulff
Oxidative stress and inherited cataracts in mice.
Ophthalmic research 1989;21(6):414-9.
1989: Jochen Graw; P M Gopinath; W Bors; C Michel; H K Summer
Biochemical analysis of young rats homozygous for the cataract mutation cat.
Experimental eye research 1989;48(1):1-9.
1986: Jochen Graw; Jack Favor; Angelika Neuhäuser-Klaus; U H Ehling
Dominant cataract and recessive specific locus mutations in offspring of X-irradiated male mice.
Mutation research 1986;159(1-2):47-54.
1985: Jochen Graw; K H Summer; C Michel; W Bors
Catalase and superoxide dismutase activities in lenses of cataractous Nop-mice.
Experimental eye research 1985;41(4):577-9.
1985: U H Ehling; D J Charles; Jack Favor; Jochen Graw; J Kratochvilova; Angelika Neuhäuser-Klaus; Walter Pretsch
Induction of gene mutations in mice: the multiple endpoint approach.
Mutation research 1985;150(1-2):393-401.
1984: Jochen Graw; J Kratochvilova; K H Summer
Genetical and biochemical studies of a dominant cataract mutant in mice.
Experimental eye research 1984;39(1):37-45.