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Results: 1-25 | 26-30
Results: 1-25/30
EQUAL METHYLATION OF HUMAN MALE AND FEMALE GERM-CELLS EXCLUDES DIFFERENTIAL METHYLATION OF CPG SITES AS MAJOR FORCE FOR MALE DRIVEN EVOLUTION
Authors: ELMAARRI O OLEK A BALABAN B MONTAG M URMAN B OLEK K CAGLAYAN SH WALTER J OLDENBURG J
Citation: O. Elmaarri et al., EQUAL METHYLATION OF HUMAN MALE AND FEMALE GERM-CELLS EXCLUDES DIFFERENTIAL METHYLATION OF CPG SITES AS MAJOR FORCE FOR MALE DRIVEN EVOLUTION, European journal of human genetics, 6, 1998, pp. 4156-4156
NOVEL MUTATIONS IN TURKISH HEMOPHILIA-A PATIENTS
Authors: TIMUR AA AKTUGLU G GURGEY A KAVAKLI K OLEK K CAGLAYAN SH
Citation: Aa. Timur et al., NOVEL MUTATIONS IN TURKISH HEMOPHILIA-A PATIENTS, European journal of human genetics, 6, 1998, pp. 4203-4203
COMPARISON BETWEEN INTRATRACHEAL AND INTRAVENOUS ADMINISTRATION OF LIPOSOME-DNA COMPLEXES FOR CYSTIC-FIBROSIS LUNG GENE-THERAPY
Authors: GRIESENBACH U CHONN A CASSADY R HANNAM V ACKERLEY C POST M TANSWELL AK OLEK K OBRODOVICH H TSUI LC
Citation: U. Griesenbach et al., COMPARISON BETWEEN INTRATRACHEAL AND INTRAVENOUS ADMINISTRATION OF LIPOSOME-DNA COMPLEXES FOR CYSTIC-FIBROSIS LUNG GENE-THERAPY, Gene therapy, 5(2), 1998, pp. 181-188
EFFICIENCY OF MICROSATELLITE MARKERS OF THE INTERNATIONAL STANDARD PANEL FOR PARENTAGE CONTROL IN GERMAN HORSE POPULATION
Authors: WIMMERS K PONSUKSILI S SCHMOLL F HARDGE T HATZIPANAGIOTOU A WEBER J WOSTMANN S OLEK K SCHELLANDER K
Citation: K. Wimmers et al., EFFICIENCY OF MICROSATELLITE MARKERS OF THE INTERNATIONAL STANDARD PANEL FOR PARENTAGE CONTROL IN GERMAN HORSE POPULATION, Zuchtungskunde, 70(4), 1998, pp. 233-241
METHYLATION LEVELS AT SELECTED CPG SITES IN THE FACTOR-VIII AND FGFR3GENES, IN MATURE FEMALE AND MALE GERM-CELLS - IMPLICATIONS FOR MALE-DRIVEN EVOLUTION
Authors: ELMAARRI O OLEK A BALABAN B MONTAG M VANDERVEN H URMAN B OLEK K CAGLAYAN SH WALTER J OLDENBURG J
Citation: O. Elmaarri et al., METHYLATION LEVELS AT SELECTED CPG SITES IN THE FACTOR-VIII AND FGFR3GENES, IN MATURE FEMALE AND MALE GERM-CELLS - IMPLICATIONS FOR MALE-DRIVEN EVOLUTION, American journal of human genetics, 63(4), 1998, pp. 1001-1008
POINT MUTATIONS IDENTIFIED IN TURKISH HEMOPHILIA-A PATIENTS USING DENATURING GRADIENT GEL-ELECTROPHORESIS (DGGE)
Authors: TIMUR A CAGLAYAN SH AKTUGLU G GURGEY A OLEK K
Citation: A. Timur et al., POINT MUTATIONS IDENTIFIED IN TURKISH HEMOPHILIA-A PATIENTS USING DENATURING GRADIENT GEL-ELECTROPHORESIS (DGGE), Thrombosis and haemostasis, 1997, pp. 926-926
MATERNAL TRANSMISSION OF BOVINE SPONGIFORM ENCEPHALOPATHY IN THE CASEOF GALLOWAY CATTLE CINDY DISPROVED
Authors: BAUMGARTNER BG MARGAN U OLEK K WAGNER V BRENIG B
Citation: Bg. Baumgartner et al., MATERNAL TRANSMISSION OF BOVINE SPONGIFORM ENCEPHALOPATHY IN THE CASEOF GALLOWAY CATTLE CINDY DISPROVED, Berliner und Munchener Tierarztliche Wochenschrift, 110(9), 1997, pp. 305-310
CYSTIC-FIBROSIS IN ARGENTINA - THE FREQUENCY OF THE DELTA-F508 MUTATION
Authors: LUNA MC GRANADOS PA OLEK K PIVETTA OH
Citation: Mc. Luna et al., CYSTIC-FIBROSIS IN ARGENTINA - THE FREQUENCY OF THE DELTA-F508 MUTATION, Human genetics, 97(3), 1996, pp. 314-314
CHARACTERIZATION OF THE FACTOR-VIII DEFECT IN 147 PATIENTS WITH SPORADIC HEMOPHILIA-A - FAMILY STUDIES INDICATE A MUTATION TYPE-DEPENDENT SEX-RATIO OF MUTATION FREQUENCIES
Authors: BECKER J SCHWAAB R MOLLERTAUBE A SCHWAAB U SCHMIDT W BRACKMANN HH GRIMM T OLEK K OLDENBURG J
Citation: J. Becker et al., CHARACTERIZATION OF THE FACTOR-VIII DEFECT IN 147 PATIENTS WITH SPORADIC HEMOPHILIA-A - FAMILY STUDIES INDICATE A MUTATION TYPE-DEPENDENT SEX-RATIO OF MUTATION FREQUENCIES, American journal of human genetics, 58(4), 1996, pp. 657-670
ALLELE-SPECIFIC SEQUENCING
Authors: KALININ VN OLEK K SCHMIDT W COTTON RGH
Citation: Vn. Kalinin et al., ALLELE-SPECIFIC SEQUENCING, Doklady Akademii nauk. Rossijskaa akademia nauk, 343(5), 1995, pp. 692-694
HEMOPHILIA-A - MUTATION TYPE DETERMINES RISK OF INHIBITOR FORMATION
Authors: SCHWAAB R BRACKMANN HH MEYER C SEEHAFER J KIRCHGESSER M HAACK A OLEK K TUDDENHAM EGD OLDENBURG J
Citation: R. Schwaab et al., HEMOPHILIA-A - MUTATION TYPE DETERMINES RISK OF INHIBITOR FORMATION, Thrombosis and haemostasis, 74(6), 1995, pp. 1402-1406
A POINT MUTATION IN THE ND1 MITOCHONDRIAL GENE IDENTIFIED IN A TYPE-II DIABETIC PATIENT
Authors: KALININ VN SCHMIDT W POLLER W OLEK K
Citation: Vn. Kalinin et al., A POINT MUTATION IN THE ND1 MITOCHONDRIAL GENE IDENTIFIED IN A TYPE-II DIABETIC PATIENT, Genetika, 31(8), 1995, pp. 1180-1182
CHARACTERIZATION OF MUTATIONS WITHIN THE FACTOR-VIII GENE OF 73 UNRELATED MILD AND MODERATE HEMOPHILIACS
Authors: SCHWAAB R OLDENBURG U JOHNSON DJD SCHMIDT W OLEK K BRACKMAN HH TUDDENHAM EGD
Citation: R. Schwaab et al., CHARACTERIZATION OF MUTATIONS WITHIN THE FACTOR-VIII GENE OF 73 UNRELATED MILD AND MODERATE HEMOPHILIACS, British Journal of Haematology, 91(2), 1995, pp. 458-464
HEMOPHILIA-A DIAGNOSIS BY AUTOMATED FLUORESCENT DNA DETECTION OF 10 FACTOR-VIII INTRON-13 DINUCLEOTIDE REPEAT ALLELES
Authors: KOCHHAN L LALLOZ MRA OLDENBURG J MCVEY JH OLEK K BRACKMANN HH TUDDENHAM EGD SCHWAAB R
Citation: L. Kochhan et al., HEMOPHILIA-A DIAGNOSIS BY AUTOMATED FLUORESCENT DNA DETECTION OF 10 FACTOR-VIII INTRON-13 DINUCLEOTIDE REPEAT ALLELES, Blood coagulation & fibrinolysis, 5(4), 1994, pp. 497-501
MYOTONIC-DYSTROPHY AND LIMB-GIRDLE MUSCULAR-DYSTROPHY IN ONE FAMILY
Authors: SCHRODER R BEYENBURG S WEBER J OLEK K ZIERZ S
Citation: R. Schroder et al., MYOTONIC-DYSTROPHY AND LIMB-GIRDLE MUSCULAR-DYSTROPHY IN ONE FAMILY, The Clinical investigator, 72(5), 1994, pp. 409-413
A G(-TO-T DONOR SPLICE-SITE MUTATION LEADS TO SKIPPING OF EXON-50 IN VON-WILLEBRAND-FACTOR MESSENGER-RNA(3))
Authors: MERTES G LUDWIG M FINKELNBURG B KRAWCZAK M SCHWAAB R BRACKMANN HH OLEK K
Citation: G. Mertes et al., A G(-TO-T DONOR SPLICE-SITE MUTATION LEADS TO SKIPPING OF EXON-50 IN VON-WILLEBRAND-FACTOR MESSENGER-RNA(3)), Genomics, 24(1), 1994, pp. 190-191
GENETIC-HETEROGENEITY OF SEVERE VON-WILLEBRAND DISEASE TYPE-III IN THE GERMAN POPULATION
Authors: SCHNEPPENHEIM R KREY S BERGMANN F BOCK D BUDDE U LANGE M LINDE R MITTLER U MEILI E MERTES G OLEK K PLENDL H SIMEONI E
Citation: R. Schneppenheim et al., GENETIC-HETEROGENEITY OF SEVERE VON-WILLEBRAND DISEASE TYPE-III IN THE GERMAN POPULATION, Human genetics, 94(6), 1994, pp. 640-652
HEMOPHILIA-A - DATABASE OF NUCLEOTIDE SUBSTITUTIONS, DELETIONS, INSERTIONS AND REARRANGEMENTS OF THE FACTOR-VIII GENE, 2ND EDITION (VOL 22,PG 3511, 1994)
Authors: TUDDENHAM EGD SCHWAAB R SEEHAFER J MILLAR DS GITSCHIER J HIGUCHI M BIDICHANDANI S CONNOR JM HOYER LW YOSHIOKA A PEAKE IR OLEK K KAZAZIAN HH LAVERGNE JM GIANNELLI F ANTONARAKIS SE COOPER DN
Citation: Egd. Tuddenham et al., HEMOPHILIA-A - DATABASE OF NUCLEOTIDE SUBSTITUTIONS, DELETIONS, INSERTIONS AND REARRANGEMENTS OF THE FACTOR-VIII GENE, 2ND EDITION (VOL 22,PG 3511, 1994), Nucleic acids research, 22(22), 1994, pp. 4850-4868
HEMOPHILIA-A - DATABASE OF NUCLEOTIDE SUBSTITUTIONS, DELETIONS, INSERTIONS AND REARRANGEMENTS OF THE FACTOR-VIII GENE, 2ND EDITION
Authors: TUDDENHAM EGD SCHWAAB R SEEHAFER J MILLAR DS GITSCHIER J HIGUCHI M BIDICHANDANI S CONNOR JM HOYER LW YOSHIOKA A PEAKE IR OLEK K KAZAZIAN HH LAVERGNE JM GIANNELLI F ANTONARAKIS SE COOPER DN
Citation: Egd. Tuddenham et al., HEMOPHILIA-A - DATABASE OF NUCLEOTIDE SUBSTITUTIONS, DELETIONS, INSERTIONS AND REARRANGEMENTS OF THE FACTOR-VIII GENE, 2ND EDITION, Nucleic acids research, 22(17), 1994, pp. 3511-3533
IDENTIFICATION AND DNA-SEQUENCE ANALYSIS OF 15 NEW ALPHA(1)-ANTITRYPSIN VARIANTS, INCLUDING 2 PI-ASTERISK-Q0 ALLELES AND ONE DEFICIENT PI-ASTERISK-M ALLELE
Authors: FABER JP POLLER W WEIDINGER S KIRCHGESSER M SCHWAAB R BIDLINGMAIER F OLEK K
Citation: Jp. Faber et al., IDENTIFICATION AND DNA-SEQUENCE ANALYSIS OF 15 NEW ALPHA(1)-ANTITRYPSIN VARIANTS, INCLUDING 2 PI-ASTERISK-Q0 ALLELES AND ONE DEFICIENT PI-ASTERISK-M ALLELE, American journal of human genetics, 55(6), 1994, pp. 1113-1121
A LEUCINE-TO-PROLINE SUBSTITUTION CAUSES A DEFECTIVE ALPHA(1)-ANTICHYMOTRYPSIN ALLELE ASSOCIATED WITH FAMILIAL OBSTRUCTIVE LUNG-DISEASE
Authors: POLLER W FABER JP WEIDINGER S TIEF K SCHOLZ S FISCHER M OLEK K KIRCHGESSER M HEIDTMANN HH
Citation: W. Poller et al., A LEUCINE-TO-PROLINE SUBSTITUTION CAUSES A DEFECTIVE ALPHA(1)-ANTICHYMOTRYPSIN ALLELE ASSOCIATED WITH FAMILIAL OBSTRUCTIVE LUNG-DISEASE, Genomics, 17(3), 1993, pp. 740-743
RECURRENT MUTATIONS IN THE FACTOR-IX GENE - FOUNDER EFFECT OR REPEAT DE-NOVO EVENTS - INVESTIGATION OF THE GERMAN HEMOPHILIA-B POPULATION AND REVIEW OF DE-NOVO MUTATIONS
Authors: KNOBLOCH O ZOLL B ZERRES K BRACKMANN HH OLEK K LUDWIG M
Citation: O. Knobloch et al., RECURRENT MUTATIONS IN THE FACTOR-IX GENE - FOUNDER EFFECT OR REPEAT DE-NOVO EVENTS - INVESTIGATION OF THE GERMAN HEMOPHILIA-B POPULATION AND REVIEW OF DE-NOVO MUTATIONS, Human genetics, 92(1), 1993, pp. 40-48
DELTA-C IN EXON-18 OF THE VON-WILLEBRAND GENE IS UNCOMMON IN GERMAN VWD TYPE-III PATIENTS
Authors: MERTES G LUDWIG M SCHWAAB R BRACKMANN HH OLEK K
Citation: G. Mertes et al., DELTA-C IN EXON-18 OF THE VON-WILLEBRAND GENE IS UNCOMMON IN GERMAN VWD TYPE-III PATIENTS, Thrombosis and haemostasis, 70(6), 1993, pp. 1064-1065
THE MOLECULAR-BASIS OF ALPHA(1)-ANTICHYMOTRYPSIN DEFICIENCY IN A HETEROZYGOTE WITH LIVER AND LUNG-DISEASE
Authors: FABER JP POLLER W OLEK K BAUMANN U CARLSON J LINDMARK B ERIKSSON S
Citation: Jp. Faber et al., THE MOLECULAR-BASIS OF ALPHA(1)-ANTICHYMOTRYPSIN DEFICIENCY IN A HETEROZYGOTE WITH LIVER AND LUNG-DISEASE, Journal of hepatology, 18(3), 1993, pp. 313-321
GENE SCANNING OF GLUCOKINASE IN GERMAN EARLY AND LATE AGE-OF-ONSET NIDDM FAMILIES
Authors: HAGER J FROQUEL P VELHO G OLEK K POLLER W
Citation: J. Hager et al., GENE SCANNING OF GLUCOKINASE IN GERMAN EARLY AND LATE AGE-OF-ONSET NIDDM FAMILIES, Diabetologia, 36, 1993, pp. 10000084-10000084
Risultati: 1-25 | 26-30