AAAAAA

   
Results: 1-12 |
Results: 12
SUBTYPING ANALYSIS OF FANCONI-ANEMIA BY IMMUNOBLOTTING AND RETROVIRALGENE-TRANSFER
Authors: PULSIPHER M KUPFER GM NAF D SULIMAN A LEE JS JAKOBS P GROMPE M JOENJE H SIEFF C GUINAN E MULLIGAN R DANDREA AD
Citation: M. Pulsipher et al., SUBTYPING ANALYSIS OF FANCONI-ANEMIA BY IMMUNOBLOTTING AND RETROVIRALGENE-TRANSFER, Molecular medicine (Cambridge, Mass.), 4(7), 1998, pp. 468-479
A CONGENITAL-MALFORMATION OF THE SYSTEMIC HEART COMPLEX IN SEPIA-OFFICINALIS L. (CEPHALOPODA)
Authors: SCHIPP R VONBOLETZKY S JAKOBS P LABOURG PJ
Citation: R. Schipp et al., A CONGENITAL-MALFORMATION OF THE SYSTEMIC HEART COMPLEX IN SEPIA-OFFICINALIS L. (CEPHALOPODA), Helgolander Meeresuntersuchungen, 52(1), 1998, pp. 29-40
FUNCTIONALLY ACTIVE RETROVIRAL VECTORS FOR SUBTYPING ANALYSIS AND GENE-THERAPY IN FANCONI-ANEMIA
Authors: PULSIPHER M KUPFER GM NAF D SULIMAN A JAKOBS P GROMPE M MULLIGAN R SIEFF C DANDREA AD
Citation: M. Pulsipher et al., FUNCTIONALLY ACTIVE RETROVIRAL VECTORS FOR SUBTYPING ANALYSIS AND GENE-THERAPY IN FANCONI-ANEMIA, Blood, 90(10), 1997, pp. 1049-1049
TREATMENT OF PEPTIC-ULCERS USING A SPECIFIC FORMULATION OF POLYDIMETHYLSILOXANE (UCD)
Authors: GROITL H SCHMIDT A UPMEYER HJ JAKOBS P
Citation: H. Groitl et al., TREATMENT OF PEPTIC-ULCERS USING A SPECIFIC FORMULATION OF POLYDIMETHYLSILOXANE (UCD), Gastroenterology, 110(4), 1996, pp. 124-124
SPONTANEOUS DELETION IN THE FMR1 GENE IN A PATIENT WITH FRAGILE-X SYNDROME AND CHERUBISM
Authors: QUAN F GROMPE M JAKOBS P POPOVICH BW
Citation: F. Quan et al., SPONTANEOUS DELETION IN THE FMR1 GENE IN A PATIENT WITH FRAGILE-X SYNDROME AND CHERUBISM, Human molecular genetics, 4(9), 1995, pp. 1681-1684
MICROCELL MEDIATED CHROMOSOME TRANSFER MAPS A FANCONI-ANEMIA GROUP-D COMPLEMENTING GENE TO CHROMOSOME 3P
Authors: WHITNEY MA THAYER M RIEFSTECK C OLSON S SMITH L JAKOBS P LEACH R NAYLOR S JOENJE H GROMPE M
Citation: Ma. Whitney et al., MICROCELL MEDIATED CHROMOSOME TRANSFER MAPS A FANCONI-ANEMIA GROUP-D COMPLEMENTING GENE TO CHROMOSOME 3P, American journal of human genetics, 57(4), 1995, pp. 1055-1055
THE ASHKENAZI JEWISH FANCONI-ANEMIA MUTATION - INCIDENCE AMONG PATIENTS AND CARRIER FREQUENCY IN THE AT-RISK POPULATION
Authors: WHITNEY MA JAKOBS P KABACK M MOSES RE GROMPE M
Citation: Ma. Whitney et al., THE ASHKENAZI JEWISH FANCONI-ANEMIA MUTATION - INCIDENCE AMONG PATIENTS AND CARRIER FREQUENCY IN THE AT-RISK POPULATION, Human mutation, 3(4), 1994, pp. 339-341
LABELING OF A PUTATIVE MG2-ATPASE GIVES EVIDENCE OF CA2+ CONTROL OF THE MG2+ SITE AFFINITY( SITE ON THE SR CA)
Authors: COAN C JAKOBS P JI JY MURPHY AJ
Citation: C. Coan et al., LABELING OF A PUTATIVE MG2-ATPASE GIVES EVIDENCE OF CA2+ CONTROL OF THE MG2+ SITE AFFINITY( SITE ON THE SR CA), Biophysical journal, 66(2), 1994, pp. 10000120-10000120
MUTATIONS IN FACC ACCOUNT FOR APPROXIMATELY 25-PERCENT OF FANCONI-ANEMIA
Authors: WHITNEY M SAITO H JAKOBS P MOSES RE GROMPE M
Citation: M. Whitney et al., MUTATIONS IN FACC ACCOUNT FOR APPROXIMATELY 25-PERCENT OF FANCONI-ANEMIA, Experimental hematology, 21(5), 1993, pp. 720-720
SARCOPLASMIC-RETICULUM CALCIUM-ATPASE - LABELING OF A PUTATIVE MG2-LABEL( SITE BY REACTION WITH A CARBODIIMIDE AND A SPIN)
Authors: COAN C JAKOBS P JI JY MURPHY AJ
Citation: C. Coan et al., SARCOPLASMIC-RETICULUM CALCIUM-ATPASE - LABELING OF A PUTATIVE MG2-LABEL( SITE BY REACTION WITH A CARBODIIMIDE AND A SPIN), FEBS letters, 335(1), 1993, pp. 33-36
A COMMON MUTATION IN THE FACC GENE CAUSES FANCONI-ANEMIA IN ASHKENAZIJEWS
Authors: WHITNEY MA JAKOBS P KABACK M MOSES RE GROMPE M
Citation: Ma. Whitney et al., A COMMON MUTATION IN THE FACC GENE CAUSES FANCONI-ANEMIA IN ASHKENAZIJEWS, American journal of human genetics, 53(3), 1993, pp. 12-12
PHENOTYPIC COMPLEMENTATION OF FANCONI-ANEMIA FIBROBLASTS BY CDNA
Authors: MOSES RE WHITNEY M GROMPE M MERKENS L JAKOBS P HEJNA J TITTLE T
Citation: Re. Moses et al., PHENOTYPIC COMPLEMENTATION OF FANCONI-ANEMIA FIBROBLASTS BY CDNA, American journal of human genetics, 53(3), 1993, pp. 714-714
Risultati: 1-12 |