Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Lori D, Hill"'
Autor:
Lori D Hill, Timothy P York, Juan P Kusanovic, Ricardo Gomez, Lindon J Eaves, Roberto Romero, Jerome F Strauss
Publikováno v:
PLoS ONE, Vol 6, Iss 1, p e16681 (2011)
Preeclampsia is a leading cause of perinatal morbidity and mortality. This disorder is thought to be multifactorial in origin, with multiple genes, environmental and social factors, contributing to disease. One proposed mechanism is placental hypoxia
Externí odkaz:
https://doaj.org/article/d0576cdbb18845f294dbb11d24804295
Autor:
Roberto Romero, Ricardo Gomez, Jerome F. Strauss, Michal A. Elovitz, Maria E. Teves, Derek L. Vanhille, DaShaunda D. Hilliard, Eun D. Lee, Efstratios Stratikos, Juan Pedro Kusanovic, Sindhu K. Srinivas, Lori D. Hill
Publikováno v:
Molecular Genetics & Genomic Medicine. 1:98-107
Single nucleotide polymorphisms (SNPs) in the endoplasmic reticulum aminopeptidase 2 (ERAP2) gene are associated with preeclampsia (PE) in different populations. rs2549782, a coding variant (N392K) that significantly affects substrate specificity, is
Autor:
Derek L, Vanhille, Lori D, Hill, Dashaunda D, Hilliard, Eun D, Lee, Maria E, Teves, Sindhu, Srinivas, Juan P, Kusanovic, Ricardo, Gomez, Efstratios, Stratikos, Michal A, Elovitz, Roberto, Romero, Jerome F, Strauss
Publikováno v:
Molecular Genetics & Genomic Medicine
Single nucleotide polymorphisms (SNPs) in the endoplasmic reticulum aminopeptidase 2 (ERAP2) gene are associated with preeclampsia (PE) in different populations. rs2549782, a coding variant (N392K) that significantly affects substrate specificity, is
Autor:
Jerome F. Strauss, Kathryn G. Ewens, Timothy P. York, Lori D. Hill, Andrea Dunaif, Brion S. Maher, Richard S. Legro
Polycystic ovary syndrome (PCOS) is an endocrine disorder that affects 5–8% of reproductive age women. The primary features of PCOS are hyperandrogenemia, chronic anovulation and infertility. It has been suggested that defects in ovarian steroid me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7c07f6d2b8127e0af7791b28f9b62e9
https://europepmc.org/articles/PMC3264817/
https://europepmc.org/articles/PMC3264817/
Autor:
Lindon J. Eaves, Roberto Romero, Ricardo Gomez, Juan Pedro Kusanovic, Jerome F. Strauss, Lori D. Hill, Timothy P. York
Publikováno v:
PLoS ONE
PLoS ONE, Vol 6, Iss 1, p e16681 (2011)
PLoS ONE, Vol 6, Iss 1, p e16681 (2011)
Preeclampsia is a leading cause of perinatal morbidity and mortality. This disorder is thought to be multifactorial in origin, with multiple genes, environmental and social factors, contributing to disease. One proposed mechanism is placental hypoxia
Publikováno v:
American journal of obstetrics and gynecology. 202(5)
We sought to determine allele frequencies of 3 LAMC1 single nucleotide polymorphisms (SNPs) in Caucasian and African American (AA) women with stageII pelvic organ prolapse (POP) (cases) and in ethnicity-matched controls with stageII POP. We also soug
To identify candidate genes contributing to preterm birth, we examined the existing literature on the association between known disorders of connective tissue synthesis and metabolism and related diseases and prematurity. Our hypothesis was that abno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f66ad7c843fae9865a536b7a97ed4d4f
https://europepmc.org/articles/PMC2673455/
https://europepmc.org/articles/PMC2673455/
Autor:
Derek L. Vanhille, Lori D. Hill, DaShaunda D. Hilliard, Eun D. Lee, Maria E. Teves, Sindhu Srinivas, Juan P. Kusanovic, Ricardo Gomez, Efstratios Stratikos, Michal A. Elovitz, Roberto Romero, Jerome F. Strauss
Publikováno v:
Molecular Genetics & Genomic Medicine
Autor:
David R. Nagarkatti-Gude, Giulia Collodel, Elena Moretti, Michela Geminiani, Zhibing Zhang, Lori D. Hill, Jerome F. Strauss
Publikováno v:
BMC Urology
BMC Urology, Vol 12, Iss 1, p 27 (2012)
BMC Urology, Vol 12, Iss 1, p 27 (2012)
Background SPAG16 is a critical structural component of motile cilia and flagella. In the eukaryotic unicellular algae Chlamydomonas, loss of gene function causes flagellar paralysis and prevents assembly of the “9 + 2” axoneme central pair. In m
Autor:
Roberto Romero, Ricardo Gomez, Juan Pedro Kusanovic, DaShaunda D. Hilliard, Michal A. Elovitz, Timothy P. York, Sindhu K. Srinivas, Lori D. Hill, Jerome F. Strauss
Publikováno v:
BMC Medical Genetics, Vol 12, Iss 1, p 64 (2011)
BMC Medical Genetics
BMC Medical Genetics
Background Preeclampsia affects 3-8% of pregnancies and is a major cause of maternal and perinatal morbidity and mortality worldwide. This complex disorder is characterized by alterations in the immune and vascular systems and involves multiple organ