Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Heather R. Glatt-Deeley"'
Autor:
Darcy T. Ahern, Prakhar Bansal, Isaac V. Faustino, Heather R. Glatt-Deeley, Yuvabharath Kondaveeti, Erin C. Banda, Stefan F. Pinter
Publikováno v:
bioRxiv
SUMMARYModeling the developmental etiology of viable human aneuploidies can be challenging in rodent models, where synteny with human chromosomes is affected, or primate-specific biology is implicated. In humans, monosomy-X (45,X) causes Turner syndr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f6eb39f2faca93764e1857fc6ec2e17
https://doi.org/10.1101/2023.03.08.531747
https://doi.org/10.1101/2023.03.08.531747
Autor:
Darcy T. Ahern, Prakhar Bansal, Maria K. Armillei, Isaac V. Faustino, Yuvabharath Kondaveeti, Heather R. Glatt-Deeley, Erin C. Banda, Stefan F. Pinter
Publikováno v:
Proceedings of the National Academy of Sciences. 119
Mammalian sex chromosomes encode homologous X/Y gene pairs that were retained on the Y chromosome in males and escape X chromosome inactivation (XCI) in females. Inferred to reflect X/Y pair dosage sensitivity, monosomy X is a leading cause of miscar
Autor:
Prakhar Bansal, Erin. C Banda, Heather R. Glatt-Deeley, Christopher E. Stoddard, Darcy T. Ahern, Yuvabharath Kondaveeti, Michael Nicouleau, Stefan F. Pinter
/SUMMARYExcess gene dosage from human chromosome 21 (HSA21), due to trisomy or translocation of HSA21 material, causes Down syndrome (DS). Trisomy 21 (T21) results in a large number of developmental and ongoing cellular phenotypes, raising the critic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3691792e575afcb33eb0cb95f631cb1
https://doi.org/10.1101/2022.05.11.491519
https://doi.org/10.1101/2022.05.11.491519
Autor:
Darcy T. Ahern, Prakhar Bansal, Isaac Faustino, Yuvabharath Kondaveeti, Heather R. Glatt-Deeley, Erin C. Banda, Stefan F. Pinter
SUMMARY/ABSTRACTMammalian sex chromosomes encode homologous X/Y gene pairs that were retained on the male Y and escape X chromosome inactivation (XCI) in females. Inferred to reflect X/Y-pair dosage sensitivity, monosomy X is a leading cause of misca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2173dcbddc4b89598017766b17dec6c
https://doi.org/10.1101/2021.12.13.472325
https://doi.org/10.1101/2021.12.13.472325
Autor:
Heather R. Glatt-Deeley, Upendra P. Hegde, Richard B. Everson, Lorrie A. Perpetua, Richard W. Lambrecht, Mary M. Sanders, Linda Burian
Publikováno v:
Cancer Research. 71:3938-3938
The standard procedure for processing clinical pathology specimens for diagnostic purposes is by formalin-fixation and paraffin-embedding (FFPE). This method is used world-wide for the vast majority of routine histopathology. Nucleic acids in FFPE sp