المؤلفون: Gleeson M; Hunter Family Cancer Service, Newcastle, Australia. Electronic address: Margaret.gleeson@health.nsw.gov.au., Kentwell M; Parkville Familial Cancer Clinic, Peter MacCallum Cancer Centre and Royal Melbourne Hospital, Melbourne, Australia; The Royal Women's Hospital, Oncology and Dysplasia, Melbourne, Australia., Meiser B; Prince of Wales Clinical School, UNSW Sydney, Australia., Do J; Prince of Wales Clinical School, UNSW Sydney, Australia., Nevin S; Prince of Wales Clinical School, UNSW Sydney, Australia., Taylor N; The Cancer Council New South Wales, Sydney and Faculty of Health Science, University of Sydney, Australia., Barlow-Stewart K; Sydney Medical School, University of Sydney, Australia., Kirk J; Familial Cancer Service, Westmead Hospital, Sydney Medical School, University of Sydney and Centre for Cancer Research, The Westmead Institute for Medical Research, Australia., James P; Parkville Familial Cancer Clinic, Peter MacCallum Cancer Centre and Royal Melbourne Hospital, Melbourne, Australia., Scott CL; Parkville Familial Cancer Clinic, Peter MacCallum Cancer Centre and Royal Melbourne Hospital, Melbourne, Australia; Department of Obstetrics and Gynaecology and Department of Medical Biology, University of Melbourne, Australia., Williams R; Prince of Wales Clinical School, UNSW Sydney, Australia; Hereditary Cancer Centre, Prince of Wales Hospital, Sydney, Australia., Gamet K; Genetic Health Service NZ Northern Hub, Auckland City Hospital, Auckland, New Zealand., Burke J; Tasmanian Clinical Genetics Service, Royal Hobart Hospital, Hobart, Australia., Murphy M; Parkville Familial Cancer Clinic, Peter MacCallum Cancer Centre and Royal Melbourne Hospital, Melbourne, Australia; Bendigo Health Cancer Centre, Bendigo, Australia., Antill YC; Parkville Familial Cancer Clinic, Peter MacCallum Cancer Centre and Royal Melbourne Hospital, Melbourne, Australia; Familial Cancer Centre, Monash Health, Victoria, Australia., Pearn A; Genetic Services of Western Australia, King Edward Memorial Hospital, Perth, Australia., Pachter N; Genetic Services of Western Australia, King Edward Memorial Hospital, Perth, Australia; School of Medicine, University of Western Australia, Perth, Australia., Ebzery C; Genetic Health Queensland, Royal Brisbane and Women's Hospital, Queensland, Australia., Poplawski N; Adult Genetics Unit, Royal Adelaide Hospital, Adelaide and School of Medicine, University of Adelaide, Australia., Friedlander M; Dept Medical Oncology, Prince of Wales Hospital, Sydney, Australia., Tucker KM; Prince of Wales Clinical School, UNSW Sydney, Australia; Hereditary Cancer Centre, Prince of Wales Hospital, Sydney, Australia.

مؤلفون مشاركون: Australian Genetic Testing Mainstreaming Collaborative Group

المصدر: Gynecologic oncology [Gynecol Oncol] 2020 Aug; Vol. 158 (2), pp. 431-439. Date of Electronic Publication: 2020 May 22.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Academic Press Country of Publication: United States NLM ID: 0365304 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1095-6859 (Electronic) Linking ISSN: 00908258 NLM ISO Abbreviation: Gynecol Oncol Subsets: MEDLINE

مواضيع طبية MeSH: Carcinoma, Ovarian Epithelial/*genetics , Genetic Testing/*methods , Genetics/*education , Medical Oncology/*education , Ovarian Neoplasms/*genetics, Adolescent ; Adult ; BRCA1 Protein/genetics ; BRCA2 Protein/genetics ; Education, Medical, Continuing ; Female ; Health Personnel/education ; Humans ; Middle Aged ; Young Adult

المؤلفون: Taylor N Ayers, Matthew L Nicotra, Miler T Lee

المصدر: PLoS Genetics, Vol 19, Iss 7, p e1010845 (2023)

مصطلحات موضوعية: Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1010845&type=printable; https://doaj.org/toc/1553-7390; https://doaj.org/toc/1553-7404

URL الوصول: https://doaj.org/article/7d28951417bc4b59aec19f5fea1a85c8

المؤلفون: Jayson J Smith, Yutong Xiao, Nithin Parsan, Taylor N Medwig-Kinney, Michael A Q Martinez, Frances E Q Moore, Nicholas J Palmisano, Abraham Q Kohrman, Mana Chandhok Delos Reyes, Rebecca C Adikes, Simeiyun Liu, Sydney A Bracht, Wan Zhang, Kailong Wen, Paschalis Kratsios, David Q Matus

المصدر: PLoS Genetics, Vol 18, Iss 1, p e1009981 (2022)

مصطلحات موضوعية: Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1553-7390; https://doaj.org/toc/1553-7404

URL الوصول: https://doaj.org/article/8272496a21d1415fbab6d79035f844d3

المؤلفون: Michael A. Q. Martinez, Brian A. Kinney, Taylor N. Medwig-Kinney, Guinevere Ashley, James M. Ragle, Londen Johnson, Joseph Aguilera, Christopher M. Hammell, Jordan D. Ward, David Q. Matus

المصدر: G3: Genes, Genomes, Genetics, Vol 10, Iss 1, Pp 267-280 (2020)

مصطلحات موضوعية: c. elegans, aid system, synthetic auxin, microfluidics, scf complex, nhr-25, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2160-1836

URL الوصول: https://doaj.org/article/55319c4b1897467ba7f8b7a022aaf70a

المؤلفون: Michael S. Adamowicz, Taylor N. Rambo, Jennifer L. Clarke

المصدر: Genes, Vol 13, Iss 8, p 1429 (2022)

مصطلحات موضوعية: probabilistic genotyping, DNA mixtures, STR analysis, likelihood ratios, MaSTR™, validation, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://www.mdpi.com/2073-4425/13/8/1429; https://doaj.org/toc/2073-4425

URL الوصول: https://doaj.org/article/f51de28da6a54136b2e43ddb622f299e

المؤلفون: Noémi Dahan-Oliel, Klaus Dieterich, Frank Rauch, Ghalib Bardai, Taylor N. Blondell, Anxhela Gjyshi Gustafson, Reggie Hamdy, Xenia Latypova, Kamran Shazand, Philip F. Giampietro, Harold van Bosse

المصدر: Genes, Vol 12, Iss 8, p 1220 (2021)

مصطلحات موضوعية: CHRNG, distal arthrogryposis type 8, Escobar, multiple pterygium syndrome, MYH3, scoliosis, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://www.mdpi.com/2073-4425/12/8/1220; https://doaj.org/toc/2073-4425

URL الوصول: https://doaj.org/article/50605aca30f04372b843e6f9f73fb44e

المؤلفون: Campbell, Susan B., Leezenbaum, Nina B., Mahoney, Amanda S., Day, Taylor N., Schmidt, Emily N.

المصدر: Autism: The International Journal of Research and Practice. Nov 2015 19(8):915-924.

Peer Reviewed: Y

Page Count: 10

Sponsoring Agency: Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) (NIH)
National Institutes of Health (DHHS)
National Institute of Mental Health (DHHS/NIH)

Descriptors: Autism, Pervasive Developmental Disorders, Infants, Siblings, At Risk Persons, Genetics, Parent Child Relationship, Parents, Diagnostic Tests, Observation, Severity (of Disability), Play, Young Children, Cognitive Ability, Motor Development

مصطلحات جغرافية: Pennsylvania

Assessment and Survey Identifiers: Mullen Scales of Early Learning, Autism Diagnostic Observation Schedule

المؤلفون: Hills-Muckey, Kelly, Martinez, Michael AQ, Stec, Natalia, Hebbar, Shilpa, Saldanha, Joanne, Medwig-Kinney, Taylor N, Moore, Frances EQ, Ivanova, Maria, Morao, Ana, Ward, JD, Moss, Eric G, Ercan, Sevinc, Zinovyeva, Anna Y, Matus, David Q, Hammell, Christopher M

المصدر: Genetics. 220(2)

مصطلحات موضوعية: Biochemistry and Cell Biology, Biological Sciences, Biotechnology, Bioengineering, Animals, Arabidopsis, Arabidopsis Proteins, Caenorhabditis elegans, Caenorhabditis elegans Proteins, F-Box Proteins, Indoleacetic Acids, C, elegans, AID system, CRISPR, Cas9, targeted degradation, heterochronic, RNA pol II inhibition, auxin, C. elegans, CRISPR/Cas9, Genetics, Developmental Biology, Biochemistry and cell biology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/4rj5p502

المؤلفون: Ashley, Guinevere E, Duong, Tam, Levenson, Max T, Martinez, Michael AQ, Johnson, Londen C, Hibshman, Jonathan D, Saeger, Hannah N, Palmisano, Nicholas J, Doonan, Ryan, Martinez-Mendez, Raquel, Davidson, Brittany R, Zhang, Wan, Ragle, James Matthew, Medwig-Kinney, Taylor N, Sirota, Sydney S, Goldstein, Bob, Matus, David Q, Dickinson, Daniel J, Reiner, David J, Ward, Jordan D

المصدر: Genetics. 217(3)

مصطلحات موضوعية: Genetics, Biotechnology, Generic health relevance, Animals, Arabidopsis Proteins, CRISPR-Cas Systems, Caenorhabditis elegans, Caenorhabditis elegans Proteins, F-Box Proteins, Genes, Reporter, Genetic Engineering, Indoleacetic Acids, Luminescent Proteins, Organ Specificity, Proteolysis, Receptors, Cell Surface, Transgenes, C. elegans, AID system, SapTrap, self-excising cassette, CRISPR/Cas9, Transport Inhibitor Response 1, C. elegans, Developmental Biology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/1384d9wp

المؤلفون: Martinez, Michael AQ, Kinney, Brian A, Medwig-Kinney, Taylor N, Ashley, Guinevere, Ragle, James M, Johnson, Londen, Aguilera, Joseph, Hammell, Christopher M, Ward, Jordan D, Matus, David Q

المصدر: G3 (Bethesda, Md.). 10(1)

مصطلحات موضوعية: Animals, Caenorhabditis elegans, Indoleacetic Acids, Naphthaleneacetic Acids, Ubiquitin-Protein Ligases, Caenorhabditis elegans Proteins, Microfluidics, Larva, Single-Cell Analysis, Proteolysis, AID system, C. elegans, NHR-25, SCF complex, microfluidics, synthetic auxin, Genetics

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/13c71113