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발행년	- (예 : 2010-2015)

전체선택

Medieval DNA from Soqotra points to Eurasian origins of an isolated population at the crossroads of Africa and Arabia.

Academic Journal

Sirak, Kendra; Jansen Van Rensburg, Julian; Brielle, Esther; Chen, Bowen; Lazaridis, Iosif; Ringbauer, Harald; Mah, Matthew; Mallick, Swapan; Micco, Adam; Rohland, Nadin; Callan, Kimberly; Curtis, Elizabeth; Kearns, Aisling; Lawson, Ann Marie; Workman, J. Noah; Zalzala, Fatma; Ahmed Al-Orqbi, Ahmed Saeed; Ahmed Salem, Esmail Mohammed; Salem Hasan, Ali Mohammed; Britton, Daniel Charles

Nature Ecology & Evolution; Apr2024, Vol. 8 Issue 4, p817-829, 13p

Web of Science JCR 저널정보 Scopus Find it@PNU

Targeted in situ cross-linking mass spectrometry and integrative modeling reveal the architectures of three proteins from SARS-CoV-2

Academic Journal

Slavin, Moriya; Zamel, Joanna; Zohar, Keren; Eliyahu, Tsiona; Braitbard, Merav; Brielle, Esther; Baraz, Leah; Stolovich-Rain, Miri; Friedman, Ahuva; Wolf, Dana G.; Rouvinski, Alexander; Linial, Michal; Schneidman-Duhovny, Dina; Kalisman, Nir

Proceedings of the National Academy of Sciences of the United States. August 24, 2021, Vol. 118 Issue 34, p1aj, 9 p.

Full Text (PNAS) Open Access (EBSCO) Web of Science JCR 저널정보 Scopus Find it@PNU

De novo STXBP1 mutation in a child with developmental delay and spasticity reveals a major structural alteration in the interface with syntaxin 1A.

Academic Journal

Banne, Ehud; Falik‐Zaccai, Tzipora; Brielle, Esther; Kalfon, Limor; Ladany, Hagay; Klinger, Danielle; Schneidman‐Duhovny, Dina; Linial, Michal

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics; Oct2020, Vol. 183 Issue 7, p412-422, 11p

Full Text (Wiley Journals) Full Text (Wiley-DB) Web of Science JCR 저널정보 Scopus Find it@PNU

De novo STXBP1mutation in a child with developmental delay and spasticity reveals a major structural alteration in the interface with syntaxin 1A

Periodical

Banne, Ehud; Falik‐Zaccai, Tzipora; Brielle, Esther; Kalfon, Limor; Ladany, Hagay; Klinger, Danielle; Schneidman‐Duhovny, Dina; Linial, Michal

American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics: The Official Publication of the International Society of Psychiatric Genetics; October 2020, Vol. 183 Issue: 7 p412-422, 11p

Full Text (Wiley Journals) Full Text (Wiley-DB) Web of Science JCR 저널정보 Scopus Find it@PNU

De novoSTXBP1mutation in a child with developmental delay and spasticity reveals a major structural alteration in the interface with syntaxin1A

Academic Journal

Banne, Ehud; Falik-Zaccai, Tzipora; Brielle, Esther; Kalfon, Limor; Ladany, Hagay; Klinger, Danielle; Schneidman-Duhovny, Dina; Linial, Michal

AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS; OCT 2020, 183 7, p412-p422, 11p.

Full Text (Wiley Journals) Full Text (Wiley-DB) Web of Science JCR 저널정보 Scopus Find it@PNU

HX TO MEASURE MEMBRANE PROTEIN ELECTROSTATICS

Academic Journal

Brielle, Esther; Arkin, Isaiah T.

PROTEIN SCIENCE; SEP 2019, 28 p197-p197, 1p. Supplement: 1

Full Text (Wiley Journals) Full Text (Wiley-DB) Web of Science JCR 저널정보 Find it@PNU

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