Zobrazeno 1 - 10
of 1 079
pro vyhledávání: '"K, Kidd"'
Autor:
Kenneth K. Kidd, Baigalmaa Evsanaa, Ariunaa Togtokh, Jane E. Brissenden, Janet M. Roscoe, Mustafa Dogan, Pavlos I. Neophytou, Cemal Gurkan, Ozlem Bulbul, Lotfi Cherni, William C. Speed, Michael Murtha, Judith R. Kidd, Andrew J. Pakstis
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-17 (2022)
Abstract Population genetic studies of North Asian ethnic groups have focused on genetic variation of sex chromosomes and mitochondria. Studies of the extensive variation available from autosomal variation have appeared infrequently. We focus on rela
Externí odkaz:
https://doaj.org/article/864dd4e2964848f28bd1d4e64d090434
Autor:
Yuriy Baglaenko, Catriona Wagner, Vijay G. Bhoj, Petter Brodin, M. Eric Gershwin, Daniel Graham, Pietro Invernizzi, Kenneth K. Kidd, Ilya Korsunsky, Michael Levy, Andrew L. Mammen, Victor Nizet, Francisco Ramirez-Valle, Edward C. Stites, Marc S. Williams, Michael Wilson, Noel R. Rose, Virginia Ladd, Marina Sirota
Publikováno v:
Cambridge Prisms: Precision Medicine, Vol 1 (2023)
Precision Medicine is an emerging approach for disease treatment and prevention that takes into account individual variability in genes, environment, and lifestyle. Autoimmune diseases are those in which the body’s natural defense system loses disc
Externí odkaz:
https://doaj.org/article/bcf797b4c46e41e2bed7e76f1a48f825
Autor:
Souhir Mestiri, Sami Boussetta, Andrew J. Pakstis, Sarra El Kamel, Amel Ben Ammar El Gaaied, Kenneth K. Kidd, Lotfi Cherni
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 3, Pp n/a-n/a (2022)
Abstract Background The single nucleotide polymorphisms (SNPs) of the dopamine D3 receptor (DRD3), the CUB and sushi multiple domains 1 (CSMD1) and the neuregulin 1 (NRG1) genes were used to study the genetic diversity and affinity among North Africa
Externí odkaz:
https://doaj.org/article/907bcba05ac74c1790c6ba8093f328c2
Autor:
Wafa Ziadi, Sami Boussetta, Sarra Elkamel, Andrew J. Pakstis, Kenneth K. Kidd, Imen Medimegh, Amel Ben Ammar Elgaaied, Lotfi Cherni
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 8, Pp n/a-n/a (2021)
Abstract Background Only a few studies have investigated the association of single nucleotide polymorphisms in STAT3 gene with the susceptibility to cancer and response to chemotherapy. Our aim was to determine the allele frequencies of rs3869550, rs
Externí odkaz:
https://doaj.org/article/4cad437252ff41b18ce646658649addf
Autor:
S. Cormican, D. M. Connaughton, C. Kennedy, S. Murray, M. Živná, S. Kmoch, N. K. Fennelly, P. O’Kelly, K. A. Benson, E. T. Conlon, G. Cavalleri, C. Foley, B. Doyle, A. Dorman, M. A. Little, P. Lavin, K. Kidd, A. J. Bleyer, P. J. Conlon
Publikováno v:
Renal Failure, Vol 41, Iss 1, Pp 832-841 (2019)
Introduction: Autosomal dominant tubulointerstitial kidney disease (ADTKD) is a rare genetic cause of renal impairment resulting from mutations in the MUC1, UMOD, HNF1B, REN, and SEC61A1 genes. Neither the national or global prevalence of these disea
Externí odkaz:
https://doaj.org/article/b14e21a261104580bccc774c2f595a7f
Autor:
Leslie La Croix, Julie K. Kidd, Heather Walter, Deborah Stone, Daniel Ferguson, Carley Fisher-Maltese, Bweikia Steen, Colleen Vesely
Publikováno v:
Journal of Early Childhood Teacher Education. 44:216-233
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b00d1a3a8fd3212436df4350b6f0133
https://doi.org/10.1080/10901027.2023.2194246
https://doi.org/10.1080/10901027.2023.2194246
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Externí odkaz:
https://doaj.org/article/d4f486b894a74310bbb8c25400947330
Autor:
Gang, Peng, Andrew J, Pakstis, Neeru, Gandotra, Tina M, Cowan, Hongyu, Zhao, Kenneth K, Kidd, Curt, Scharfe
Publikováno v:
Molecular Genetics and Metabolism. 137:292-300
DNA polymorphic markers and self-defined ethnicity groupings are used to group individuals with shared ancient geographic ancestry. Here we studied whether ancestral relationships between individuals could be identified from metabolic screening data
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3af3c7dfe1fdf30abf3a269d957058db
https://doi.org/10.1016/j.ymgme.2022.10.002
https://doi.org/10.1016/j.ymgme.2022.10.002
Publikováno v:
Forensic Science International: Genetics Supplement Series. 8:202-204
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36d766aa07c1a865cdc4ba9d1238cc8d
https://doi.org/10.1016/j.fsigss.2022.10.035
https://doi.org/10.1016/j.fsigss.2022.10.035
Autor:
Joanne B. Weidhaas, Frank J. Slack, Steven A. Belinsky, David C. Christiani, Yong Zhu, Kenneth K. Kidd, Daniel Zelterman, Robert Homer, Trupti Kulkarni, Rajeshvari Patel, Richard E. Crowell, Elizabeth A. Burki, Li Su, Eva Straka, Roman-Ulrich Muller, Imran Babar, Sunitha Nallur, Rihong Zhai, Shuguang Leng, Elena Ratner, Lena J. Chin
Supplementary Figure 1, Tables 1-4 from A SNP in a let-7 microRNA Complementary Site in the KRAS 3′ Untranslated Region Increases Non–Small Cell Lung Cancer Risk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c5fd9018deb471f621ad24ccf2a0ba8
https://doi.org/10.1158/0008-5472.22376448.v1
https://doi.org/10.1158/0008-5472.22376448.v1
