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1
Expression of VEGF b, the inhibitory isoforms of VEGF, in malignant melanoma
Expression of VEGF b, the inhibitory isoforms of VEGF, in malignant melanoma
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Expression of VEGF b, the inhibitory isoforms of VEGF, in malignant melanoma

Pritchard-Jones, R O ; Dunn, D B A ; Qiu, Y ; Varey, A H R ; Orlando, A ; Rigby, H ; Harper, S J ; Bates, D O

British journal of cancer, 2007-07, Vol.97 (2), p.223-230 [Periódico revisado por pares]

England

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2
VEGF(121)b, a new member of the VEGF(xxx)b family of VEGF-A splice isoforms, inhibits neovascularisation and tumour growth in vivo
VEGF(121)b, a new member of the VEGF(xxx)b family of VEGF-A splice isoforms, inhibits neovascularisation and tumour growth in vivo
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VEGF(121)b, a new member of the VEGF(xxx)b family of VEGF-A splice isoforms, inhibits neovascularisation and tumour growth in vivo

Rennel, E S ; Varey, A H R ; Churchill, A J ; Wheatley, E R ; Stewart, L ; Mather, S ; Bates, D O ; Harper, S J

British journal of cancer, 2009-10, Vol.101 (7), p.1183 [Periódico revisado por pares]

England

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3
RNA-Sequencing data supports the existence of novel VEGFA splicing events but not of VEGFA xxx b isoforms
RNA-Sequencing data supports the existence of novel VEGFA splicing events but not of VEGFA xxx b isoforms
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RNA-Sequencing data supports the existence of novel VEGFA splicing events but not of VEGFA xxx b isoforms

Bridgett, Stephen ; Dellett, Margaret ; Simpson, David A

Scientific reports, 2017-03, Vol.7 (1), p.58 [Periódico revisado por pares]

England

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4
Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders
Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders
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Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders

Oetjens, M T ; Kelly, M A ; Sturm, A C ; Martin, C L ; Ledbetter, D H

Nature communications, 2019-10, Vol.10 (1), p.4897-10, Article 4897 [Periódico revisado por pares]

England: Nature Publishing Group

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5
Clinical application of noninvasive prenatal screening for sex chromosome aneuploidies in 50,301 pregnancies: initial experience in a Chinese hospital
Clinical application of noninvasive prenatal screening for sex chromosome aneuploidies in 50,301 pregnancies: initial experience in a Chinese hospital
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Clinical application of noninvasive prenatal screening for sex chromosome aneuploidies in 50,301 pregnancies: initial experience in a Chinese hospital

Deng, Cechuan ; Zhu, Qian ; Liu, Sha ; Liu, Jianlong ; Bai, Ting ; Jing, Xiaosha ; Xia, Tianyu ; Liu, Yunyun ; Cheng, Jing ; Li, Zhunduo ; Wei, Xiang ; Xing, Lingling ; Luo, Yuan ; Liu, Hongqian

Scientific reports, 2019-05, Vol.9 (1), p.7767-7767, Article 7767 [Periódico revisado por pares]

England: Nature Publishing Group

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6
Apoptosis and karyogamy in syncytia induced by the HIV-1-envelope glycoprotein complex
Apoptosis and karyogamy in syncytia induced by the HIV-1-envelope glycoprotein complex
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Apoptosis and karyogamy in syncytia induced by the HIV-1-envelope glycoprotein complex

Ferri, K F ; Jacotot, E ; Geuskens, M ; Kroemer, G

Cell death and differentiation, 2000-11, Vol.7 (11), p.1137-1139 [Periódico revisado por pares]

England: Nature Publishing Group

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7
Karyotype analysis of amniotic fluid cells and report of chromosomal abnormalities in 15,401 cases of Iranian women
Karyotype analysis of amniotic fluid cells and report of chromosomal abnormalities in 15,401 cases of Iranian women
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Karyotype analysis of amniotic fluid cells and report of chromosomal abnormalities in 15,401 cases of Iranian women

Younesi, Sarang ; Taheri Amin, Mohammad Mahdi ; Hantoushzadeh, Sedigheh ; Saadati, Pourandokht ; Jamali, Soudabeh ; Modarressi, Mohammad-Hossein ; Savad, Shahram ; Delshad, Saeed ; Amidi, Saloomeh ; Geranorimi, Taraneh ; Navidpour, Fariba ; Ghafouri-Fard, Soudeh

Scientific reports, 2021-09, Vol.11 (1), p.19402-19402, Article 19402 [Periódico revisado por pares]

England: Nature Publishing Group

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8
Is the prevalence of Klinefelter syndrome increasing?
Is the prevalence of Klinefelter syndrome increasing?
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Is the prevalence of Klinefelter syndrome increasing?

MORRIS, Joan K ; ALBERMAN, Eva ; SCOTT, Claire ; JACOBS, Patricia

European journal of human genetics : EJHG, 2008-02, Vol.16 (2), p.163-170 [Periódico revisado por pares]

Avenel, NJ: Nature Publishing

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9
Triple X syndrome: a review of the literature
Triple X syndrome: a review of the literature
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Triple X syndrome: a review of the literature

OTTER, Maarten ; SCHRANDER-STUMPEL, Constance T. R. M ; CURFS, Leopold M. G

European journal of human genetics : EJHG, 2010-03, Vol.18 (3), p.265-271 [Periódico revisado por pares]

Basingstoke: Nature Publishing Group

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10
Sex chromosome aneuploidies and copy-number variants: a further explanation for neurodevelopmental prognosis variability?
Sex chromosome aneuploidies and copy-number variants: a further explanation for neurodevelopmental prognosis variability?
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Sex chromosome aneuploidies and copy-number variants: a further explanation for neurodevelopmental prognosis variability?

Le Gall, Jessica ; Nizon, Mathilde ; Pichon, Olivier ; Andrieux, Joris ; Audebert-Bellanger, Séverine ; Baron, Sabine ; Beneteau, Claire ; Bilan, Frédéric ; Boute, Odile ; Busa, Tiffany ; Cormier-Daire, Valérie ; Ferec, Claude ; Fradin, Mélanie ; Gilbert-Dussardier, Brigitte ; Jaillard, Sylvie ; Jønch, Aia ; Martin-Coignard, Dominique ; Mercier, Sandra ; Moutton, Sébastien ; Rooryck, Caroline ; Schaefer, Elise ; Vincent, Marie ; Sanlaville, Damien ; Le Caignec, Cédric ; Jacquemont, Sébastien ; David, Albert ; Isidor, Bertrand

European journal of human genetics : EJHG, 2017-08, Vol.25 (8), p.930-934 [Periódico revisado por pares]

England: Nature Publishing Group

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