Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Mark R. Gray"'
Autor:
Xu Zhang, Balaji Ganeshan, Andrew D. Smith, William E. Carson, Sara E. Martin del Campo, Darya P. Shlapak, Mark R. Gray
Publikováno v:
American Journal of Roentgenology. 205:W283-W293
The purpose of this study was to use CT texture analysis to predict overall survival (OS) in patients with metastatic melanoma and stable disease (SD) according to the Response Evaluation Criteria in Solid Tumors (RECIST) on initial posttherapy CT im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b240f6a11670dc8fb33213dec88f3a1a
https://doi.org/10.2214/ajr.15.14315
https://doi.org/10.2214/ajr.15.14315
Autor:
Shari L. Laprise, Mark R. Gray
Publikováno v:
Gene. 391:45-52
Several approaches are used to survey genomic DNA methylation patterns, including Southern blot, PCR, and microarray strategies. All of these methods are based on the use of methylation-sensitive isoschizomer restriction enzyme pairs and/or sodium bi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cab7fef04aef20f746bec656a3213052
https://doi.org/10.1016/j.gene.2006.12.002
https://doi.org/10.1016/j.gene.2006.12.002
Publikováno v:
Fertility and Sterility. 83:1363-1371
Objective Formin-2 ( Fmn2 ) mutant mice produce oocytes with meiosis I arrest. Our aim was to describe the human FORMIN-2 ( FMN2 ) gene and to identify DNA sequence polymorphisms in patients with unexplained infertility and multiple failed IVF cycles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29aabcb2aaee493bc0353e6b5f12f14f
https://doi.org/10.1016/j.fertnstert.2004.10.051
https://doi.org/10.1016/j.fertnstert.2004.10.051
Publikováno v:
Journal of Pediatric and Adolescent Gynecology. 16:217-221
Study objective WNT7A gene mutations were evaluated as a potential cause for Mullerian duct derivative abnormalities in human females. The WNT gene family encodes glycoproteins that serve as signaling molecules during early development. The WNT7A gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7591f24a9ef74a0db7af00e9a044c1e2
https://doi.org/10.1016/s1083-3188(03)00124-4
https://doi.org/10.1016/s1083-3188(03)00124-4
Autor:
Gita P. Gidwani, Lorna S. Timmreck, Richard H. Reindollar, Bernice Allito, Elizabeth M. Rohlfs, Mark R. Gray, Ann J. Davis, Barbara Handelin
Publikováno v:
American Journal of Medical Genetics. :72-76
The relationship between cystic fibrosis transmembrane conductance regulator gene (CFTR) mutations and congenital absence of the uterus and vagina (CAUV) was examined. CFTR mutations have previously been associated with congenital bilateral absence o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::638d425d33873e63fca6a198cd4bf9ec
https://doi.org/10.1002/ajmg.a.20197
https://doi.org/10.1002/ajmg.a.20197
Autor:
Mark R. Gray, Rafael Tineo, Richard H. Reindollar, Sae H Sohn, Ann Jeanette Davis, Barbara L. Resendes, James R. Stelling
Publikováno v:
American Journal of Medical Genetics. 98:129-136
Molecular genetic techniques were used to determine if mutations in the genes encoding anti-Mullerian hormone (AMH) (also known as Mullerian inhibiting substance (MIS)) and its receptor (AMHR) are commonly present in patients with congenital absence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2b6ec066dc5d5b3646ca3cd70e574b5
https://doi.org/10.1002/1096-8628(20010115)98:2<129::aid-ajmg1021>3.0.co
https://doi.org/10.1002/1096-8628(20010115)98:2<129::aid-ajmg1021>3.0.co
Publikováno v:
Fertility and Sterility. 74:1241-1244
Objective: Imperforate hymen is an uncommon anomaly of the reproductive tract, occurring in approximately 0.1% of newborn females. The familial occurrence of imperforate hymen in a child, her mother, and her mother's monozygotic twin is reported. Des
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c55a9d88dd04ab7dda4f0313f82c24af
https://doi.org/10.1016/s0015-0282(00)01599-5
https://doi.org/10.1016/s0015-0282(00)01599-5
Publikováno v:
American Journal of Obstetrics and Gynecology. 182:785-793
Objectives: Denaturing gradient gel electrophoresis can detect single base sequence differences in deoxyribonucleic acid and methylation differences in small cloned fragments of deoxyribonucleic acid. We previously detected cell type–specific melti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d5ccd3690169faf8f6df056c8c6b708
https://doi.org/10.1016/s0002-9378(00)70327-9
https://doi.org/10.1016/s0002-9378(00)70327-9
Publikováno v:
American Journal of Obstetrics and Gynecology. 179:597-603
OBJECTIVE: Several lines of evidence suggest that expression of the WT1 transcription factor gene is necessary for normal development of the renal and male reproductive systems. Female patients with severe reproductive tract developmental defects wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69c73eb7d8baea57ab9c68e632ba6bc4
https://doi.org/10.1016/s0002-9378(98)70051-1
https://doi.org/10.1016/s0002-9378(98)70051-1
Publikováno v:
Human Mutation. 12:393-402
Denaturing gradient gel electrophoresis (DGGE) is commonly used to search for point mutations in DNA fragments amplified in vitro by the polymerase chain reaction (PCR). For the complete detection of mutations in large genes with many exons, the DGGE
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4988baeb164de9539145df76897d2aa
https://doi.org/10.1002/(sici)1098-1004(1998)12:6<393::aid-humu5>3.0.co
https://doi.org/10.1002/(sici)1098-1004(1998)12:6<393::aid-humu5>3.0.co