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Results: 1-25 | 26-38
Results: 1-25/38
LOCALIZATION OF A FANCONI-ANEMIA GENE TO CHROMOSOME 9P
Authors: SAAR K SCHINDLER D WEGNER RD REIS A WIENKER TF HOEHN H JOENJE H SPERLING K DIGWEED M
Citation: K. Saar et al., LOCALIZATION OF A FANCONI-ANEMIA GENE TO CHROMOSOME 9P, European journal of human genetics, 6(5), 1998, pp. 501-508
CHROMOSOME ANALYSIS OF A 262 YEARS PRESERVED FETUS WITH MULTIPLE CONGENITAL-MALFORMATIONS - FIRST APPLICATION OF COMPARATIVE GENOMIC HYBRIDIZATION TO ANCIENT DNA
Authors: TOENNIES H MULLER D HUMMEL S HERRMANN H SPERLING K NEITZEL H
Citation: H. Toennies et al., CHROMOSOME ANALYSIS OF A 262 YEARS PRESERVED FETUS WITH MULTIPLE CONGENITAL-MALFORMATIONS - FIRST APPLICATION OF COMPARATIVE GENOMIC HYBRIDIZATION TO ANCIENT DNA, European journal of human genetics, 6, 1998, pp. 2055-2055
UBE3A GENE-EXPRESSION IN ANGELMAN SYNDROME PATIENTS WITH IMPRINTING DEFECTS
Authors: BUERGER J HENNIES HC SPERLING K REIS A
Citation: J. Buerger et al., UBE3A GENE-EXPRESSION IN ANGELMAN SYNDROME PATIENTS WITH IMPRINTING DEFECTS, European journal of human genetics, 6, 1998, pp. 4133-4133
MUTATION ANALYSIS IN THE ATM GENE OF 67 ATAXIA-TELANGIECTASIA (A-T) PATIENTS IN GERMANY
Authors: SCHINDLER D BAUMER A BERNTHALER U SENNEFELDER H BROHM M WEBER BHF SANDOVAL N PLATZER M ROSENTHAL A SHILOH Y WEGNER RD SPERLING K DOERK T BENDIX R SKAWRAN B STUHRMANNSPANGENBERG M
Citation: D. Schindler et al., MUTATION ANALYSIS IN THE ATM GENE OF 67 ATAXIA-TELANGIECTASIA (A-T) PATIENTS IN GERMANY, European journal of human genetics, 6, 1998, pp. 4237-4237
BETA-HETEROCHROMATIN IN MAMMALS - EVIDENCE FROM STUDIES IN MICROTUS-AGRESTIS BASED ON THE EXTENSIVE ACCUMULATION OF L1 AND NON-L1 RETROPOSONS IN THE HETEROCHROMATIN
Authors: NEITZEL H KALSCHEUER V HENSCHEL S DIGWEED M SPERLING K
Citation: H. Neitzel et al., BETA-HETEROCHROMATIN IN MAMMALS - EVIDENCE FROM STUDIES IN MICROTUS-AGRESTIS BASED ON THE EXTENSIVE ACCUMULATION OF L1 AND NON-L1 RETROPOSONS IN THE HETEROCHROMATIN, Cytogenetics and cell genetics, 80(1-4), 1998, pp. 165-172
NIBRIN, A NOVEL DNA DOUBLE-STRAND BREAK REPAIR PROTEIN, IS MUTATED INNIJMEGEN BREAKAGE SYNDROME
Authors: VARON R VISSINGA C PLATZER M CEROSALETTI KM CHRZANOWSKA KH SAAR K BECKMANN G SEEMANOVA E COOPER PR NOWAK NJ STUMM M WEEMAES CMR GATTI RA WILSON RK DIGWEED M ROSENTHAL A SPERLING K CONCANNON P REIS A
Citation: R. Varon et al., NIBRIN, A NOVEL DNA DOUBLE-STRAND BREAK REPAIR PROTEIN, IS MUTATED INNIJMEGEN BREAKAGE SYNDROME, Cell, 93(3), 1998, pp. 467-476
CREATION OF MONOSOMIC DERIVATIVES OF HUMAN CULTURED-CELL LINES
Authors: CLARKE DJ GIMENEZABIAN JF TONNIES H NEITZEL E SPERLING K DOWNES CS JOHNSON RT
Citation: Dj. Clarke et al., CREATION OF MONOSOMIC DERIVATIVES OF HUMAN CULTURED-CELL LINES, Proceedings of the National Academy of Sciences of the United Statesof America, 95(1), 1998, pp. 167-171
SMALL MALFORMATIONS OF THE MIDDLE-EAR - A HEREDITARY DEFECT
Authors: THIES C SPERLING K REIS A HANDROCK M
Citation: C. Thies et al., SMALL MALFORMATIONS OF THE MIDDLE-EAR - A HEREDITARY DEFECT, HNO. Hals-, Nasen-, Ohrenarzte, 46(8), 1998, pp. 757-761
IDENTIFICATION OF MOUSE CRYSTALLINS IN 2D PROTEIN-PATTERNS BY SEQUENCING AND MASS-SPECTROMETRY - APPLICATION TO CATARACT MUTANTS
Authors: JUNGBLUT PR OTTO A FAVOR J LOWE M MULLER EC KASTNER M SPERLING K KLOSE J
Citation: Pr. Jungblut et al., IDENTIFICATION OF MOUSE CRYSTALLINS IN 2D PROTEIN-PATTERNS BY SEQUENCING AND MASS-SPECTROMETRY - APPLICATION TO CATARACT MUTANTS, FEBS letters, 435(2-3), 1998, pp. 131-137
(129)XENON NMR-STUDY OF CARBON-BLACK-FILLED-EPDM
Authors: SPERLING K VEEMAN WS LITVINOV VM
Citation: K. Sperling et al., (129)XENON NMR-STUDY OF CARBON-BLACK-FILLED-EPDM, Kautschuk und Gummi, Kunststoffe, 50(11), 1997, pp. 804-806
POSSIBLE ASSOCIATION OF THE ALLELE STATUS OF THE CS.7 HHAI POLYMORPHISM-5' OF THE CFTR GENE WITH POSTNATAL FEMALE SURVIVAL/
Authors: MACEK M MACEK M KREBSOVA A NASH E HAMOSH A REIS A VARONMATEEVA R SCHMIDTKE J MAESTRI NE SPERLING K KRAWCZAK M CUTTING GR
Citation: M. Macek et al., POSSIBLE ASSOCIATION OF THE ALLELE STATUS OF THE CS.7 HHAI POLYMORPHISM-5' OF THE CFTR GENE WITH POSTNATAL FEMALE SURVIVAL/, Human genetics, 99(5), 1997, pp. 565-572
ASSIGNMENT OF THE CHICKEN MAXGENE TO CHROMOSOME HE BY FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: NANDA I PETERS MA TAPAROWSKY EJ SPERLING K SCHMID M
Citation: I. Nanda et al., ASSIGNMENT OF THE CHICKEN MAXGENE TO CHROMOSOME HE BY FLUORESCENCE IN-SITU HYBRIDIZATION, Cytogenetics and cell genetics, 76(3-4), 1997, pp. 229-232
NIJMEGEN BREAKAGE SYNDROME CELLS FAIL TO INDUCE THE P53-MEDIATED DNA-DAMAGE RESPONSE FOLLOWING EXPOSURE TO IONIZING-RADIATION
Authors: WIM JM VUILLAUME M CHRZANOWSKA K SMEETS D SPERLING K HALL J
Citation: Jm. Wim et al., NIJMEGEN BREAKAGE SYNDROME CELLS FAIL TO INDUCE THE P53-MEDIATED DNA-DAMAGE RESPONSE FOLLOWING EXPOSURE TO IONIZING-RADIATION, Molecular and cellular biology, 17(9), 1997, pp. 5016-5022
THE USE OF XE-129 NMR-SPECTROSCOPY FOR STUDYING SOILS - A PILOT-STUDY
Authors: MAGUSIN PCMM BOLZ A SPERLING K VEEMAN WS
Citation: Pcmm. Magusin et al., THE USE OF XE-129 NMR-SPECTROSCOPY FOR STUDYING SOILS - A PILOT-STUDY, Geoderma, 80(3-4), 1997, pp. 449-462
PRENATAL-DIAGNOSIS OF AUTOSOMAL RECESSIVE LAMELLAR ICHTHYOSIS (ARLI) AND IDENTIFICATION OF NEW MUTATIONS IN TGM1
Authors: WIEBE V HENNIES HC ANTONLAMPRECHT I HAMMERSEN G ROTT HD SPERLING K REIS A
Citation: V. Wiebe et al., PRENATAL-DIAGNOSIS OF AUTOSOMAL RECESSIVE LAMELLAR ICHTHYOSIS (ARLI) AND IDENTIFICATION OF NEW MUTATIONS IN TGM1, American journal of human genetics, 61(4), 1997, pp. 947-947
AN INTEGRATED TRANSCRIPT, STS, AND RESTRICTION-SIZE BASED BAC PAC CONTIG MAP FROM THE ANGELMAN-SYNDROME REGION ON HUMAN-CHROMOSOME 15Q11-Q13/
Authors: BURGER J HENNIES HC WESSEL T BURKHARDGOTTGES E SPERLING K REIS A
Citation: J. Burger et al., AN INTEGRATED TRANSCRIPT, STS, AND RESTRICTION-SIZE BASED BAC PAC CONTIG MAP FROM THE ANGELMAN-SYNDROME REGION ON HUMAN-CHROMOSOME 15Q11-Q13/, American journal of human genetics, 61(4), 1997, pp. 1345-1345
DIFFERENT MECHANISMS AND RECURRENCE RISKS OF IMPRINTING DEFECTS IN ANGELMAN-SYNDROME
Authors: BURGER J BUITING K DITTRICH B GROSS S LICH C SPERLING K HORSTHEMKE B REIS A
Citation: J. Burger et al., DIFFERENT MECHANISMS AND RECURRENCE RISKS OF IMPRINTING DEFECTS IN ANGELMAN-SYNDROME, American journal of human genetics, 61(1), 1997, pp. 88-93
NONCOMPLEMENTATION OF RADIATION-INDUCED CHROMOSOME-ABERRATIONS IN ATAXIA-TELANGIECTASIA ATAXIA-TELANGIECTASIA-VARIANT HETERODIKARYONS/
Authors: STUMM M SPERLING K WEGNER RD
Citation: M. Stumm et al., NONCOMPLEMENTATION OF RADIATION-INDUCED CHROMOSOME-ABERRATIONS IN ATAXIA-TELANGIECTASIA ATAXIA-TELANGIECTASIA-VARIANT HETERODIKARYONS/, American journal of human genetics, 60(5), 1997, pp. 1246-1251
THE GENE FOR THE ATAXIA-TELANGIECTASIA VARIANT, NIJMEGEN BREAKAGE SYNDROME, MAPS TO A 1-CM INTERVAL ON CHROMOSOME 8Q21
Authors: SAAR K CHRZANOWSKA KH STUMM M JUNG M NURNBERG G WIENKER TF SEEMANOVA E WEGNER RD REIS A SPERLING K
Citation: K. Saar et al., THE GENE FOR THE ATAXIA-TELANGIECTASIA VARIANT, NIJMEGEN BREAKAGE SYNDROME, MAPS TO A 1-CM INTERVAL ON CHROMOSOME 8Q21, American journal of human genetics, 60(3), 1997, pp. 605-610
IDENTIFICATION OF A HELA MESSENGER-RNA FRACTION WHICH CORRECTS THE MITOMYCIN-C SENSITIVITY OF IRS1 CELLS
Authors: BENDER O JONES NJ SPERLING K DIGWEED M
Citation: O. Bender et al., IDENTIFICATION OF A HELA MESSENGER-RNA FRACTION WHICH CORRECTS THE MITOMYCIN-C SENSITIVITY OF IRS1 CELLS, Mutation research. DNA repair, 363(1), 1996, pp. 9-14
EVOLUTION OF THE GONOSOMAL HETEROCHROMATIN OF MICROTUS-AGRESTIS - RAPID AMPLIFICATION OF A LARGE, MULTIMERIC, REPEAT UNIT CONTAINING A 3.0-KB (GATA)(11)-POSITIVE, MIDDLE REPETITIVE ELEMENT
Authors: KALSCHEUER V SINGH AP NANDA I SPERLING K NEITZEL H
Citation: V. Kalscheuer et al., EVOLUTION OF THE GONOSOMAL HETEROCHROMATIN OF MICROTUS-AGRESTIS - RAPID AMPLIFICATION OF A LARGE, MULTIMERIC, REPEAT UNIT CONTAINING A 3.0-KB (GATA)(11)-POSITIVE, MIDDLE REPETITIVE ELEMENT, Cytogenetics and cell genetics, 73(3), 1996, pp. 171-178
MOLECULAR ANALYSIS OF FANCONI-ANEMIA
Authors: DIGWEED M SPERLING K
Citation: M. Digweed et K. Sperling, MOLECULAR ANALYSIS OF FANCONI-ANEMIA, BioEssays, 18(7), 1996, pp. 579-585
PARTIAL TRISOMY MONOSOMY 6Q IN FETAL CELLS AND CVS LONG-TERM CULTURE NOT PRESENT IN CVS SHORT-TERM CULTURE/
Authors: WEGNER RD SCHROCK E OBLADEN M BECKER R STUMM M SPERLING K
Citation: Rd. Wegner et al., PARTIAL TRISOMY MONOSOMY 6Q IN FETAL CELLS AND CVS LONG-TERM CULTURE NOT PRESENT IN CVS SHORT-TERM CULTURE/, Prenatal diagnosis, 16(8), 1996, pp. 741-748
PHENOTYPIC DIFFERENCES IN ANGELMAN SYNDROME PATIENTS - IMPRINTING MUTATIONS SHOW LESS FREQUENTLY MICROCEPHALY AND HYPOPIGMENTATION THAN DELETIONS
Authors: BURGER J KUNZE J SPERLING K REIS A
Citation: J. Burger et al., PHENOTYPIC DIFFERENCES IN ANGELMAN SYNDROME PATIENTS - IMPRINTING MUTATIONS SHOW LESS FREQUENTLY MICROCEPHALY AND HYPOPIGMENTATION THAN DELETIONS, American journal of medical genetics, 66(2), 1996, pp. 221-226
POSSIBLE AUTOSOMAL RECESSIVE INHERITANCE OF PROGRESSIVE HEARING-LOSS WITH STAPES FIXATION
Authors: THIES C HANDROCK M SPERLING K REIS A
Citation: C. Thies et al., POSSIBLE AUTOSOMAL RECESSIVE INHERITANCE OF PROGRESSIVE HEARING-LOSS WITH STAPES FIXATION, Journal of Medical Genetics, 33(7), 1996, pp. 597-599
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