Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

Wyszukujesz frazę ""Dewey FE"" wg kryterium: Autor


Wyświetlanie 1-2 z 2
Tytuł:
Rare variants in SOX17 are associated with pulmonary arterial hypertension with congenital heart disease.
Autorzy:
Zhu N; Department of Pediatrics, Columbia University Medical Center, New York, NY, USA.; Department of Systems Biology, Columbia University Medical Center, New York, NY, USA.
Welch CL; Department of Pediatrics, Columbia University Medical Center, New York, NY, USA.
Wang J; Department of Pediatrics, Columbia University Medical Center, New York, NY, USA.; Department of Systems Biology, Columbia University Medical Center, New York, NY, USA.
Allen PM; Department of Pediatrics, Columbia University Medical Center, New York, NY, USA.
Gonzaga-Jauregui C; Regeneron Genetics Center, Regeneron Pharmaceuticals, Tarrytown, New York, USA.
Ma L; Department of Pediatrics, Columbia University Medical Center, New York, NY, USA.
King AK; Regeneron Genetics Center, Regeneron Pharmaceuticals, Tarrytown, New York, USA.
Krishnan U; Department of Pediatrics, Columbia University Medical Center, New York, NY, USA.
Rosenzweig EB; Department of Pediatrics, Columbia University Medical Center, New York, NY, USA.; Department of Medicine, Columbia University Medical Center, New York, NY, USA.
Ivy DD; Department of Pediatric Cardiology, Children's Hospital Colorado, Denver, CO, USA.
Austin ED; Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, TN, USA.
Hamid R; Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, TN, USA.
Pauciulo MW; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.; Department of Pediatrics, University of CincinnatiCollege of Medicine, Cincinnati, OH, USA.
Lutz KA; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Nichols WC; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.; Department of Pediatrics, University of CincinnatiCollege of Medicine, Cincinnati, OH, USA.
Reid JG; Regeneron Genetics Center, Regeneron Pharmaceuticals, Tarrytown, New York, USA.
Overton JD; Regeneron Genetics Center, Regeneron Pharmaceuticals, Tarrytown, New York, USA.
Baras A; Regeneron Genetics Center, Regeneron Pharmaceuticals, Tarrytown, New York, USA.
Dewey FE; Regeneron Genetics Center, Regeneron Pharmaceuticals, Tarrytown, New York, USA.
Shen Y; Department of Systems Biology, Columbia University Medical Center, New York, NY, USA.; Department of Biomedical Informatics, Columbia University, New York, NY, USA.
Chung WK; Department of Pediatrics, Columbia University Medical Center, New York, NY, USA. .; Department of Medicine, Columbia University Medical Center, New York, NY, USA. .; Herbert Irving Comprehensive Cancer Center, Columbia University Medical Center, New York, NY, USA. .; New York, USA. .
Pokaż więcej
Źródło:
Genome medicine [Genome Med] 2018 Jul 20; Vol. 10 (1), pp. 56. Date of Electronic Publication: 2018 Jul 20.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Variation*
Heart Defects, Congenital/*complications
Heart Defects, Congenital/*genetics
Hypertension, Pulmonary/*complications
Hypertension, Pulmonary/*genetics
SOXF Transcription Factors/*genetics
Adolescent ; Adult ; Amino Acid Sequence ; Child ; Child, Preschool ; Female ; Genetic Predisposition to Disease ; Humans ; Infant ; Male ; Risk Factors ; SOXF Transcription Factors/chemistry
Czasopismo naukowe
Tytuł:
Phased whole-genome genetic risk in a family quartet using a major allele reference sequence.
Autorzy:
Dewey FE; Center for Inherited Cardiovascular Disease, Division of Cardiovascular Medicine, Stanford University, Stanford, California, USA.
Chen R
Cordero SP
Ormond KE
Caleshu C
Karczewski KJ
Whirl-Carrillo M
Wheeler MT
Dudley JT
Byrnes JK
Cornejo OE
Knowles JW
Woon M
Sangkuhl K
Gong L
Thorn CF
Hebert JM
Capriotti E
David SP
Pavlovic A
West A
Thakuria JV
Ball MP
Zaranek AW
Rehm HL
Church GM
West JS
Bustamante CD
Snyder M
Altman RB
Klein TE
Butte AJ
Ashley EA
Pokaż więcej
Źródło:
PLoS genetics [PLoS Genet] 2011 Sep; Vol. 7 (9), pp. e1002280. Date of Electronic Publication: 2011 Sep 15.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Genes, Synthetic*
Genetic Variation*
DNA Mutational Analysis/*methods
Genome-Wide Association Study/*methods
Thrombophilia/*genetics
Alleles ; Base Sequence ; Female ; Genetic Predisposition to Disease ; Genome, Human ; Genotype ; Haplotypes ; Humans ; Male ; Pedigree ; Reference Standards ; Risk Assessment ; Sequence Alignment ; Sequence Analysis, DNA
Czasopismo naukowe
    Wyświetlanie 1-2 z 2

    Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies