Comparative Study of Transcriptome in the Hearts Isolated from Mice, Rats, and Humans by Daigo Okada, Yosuke Okamoto, Toshiro Io, Miho Oka, Daiki Kobayashi, Suzuka Ito, Ryo Yamada, Kuniaki Ishii, Kyoichi Ono

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Rare dosage abnormalities flanking the SHOX gene by David J. Bunyan, Evelien Gevers, James I. Hobbs, Philippa J. Duncan-Flavell, Rachel J. Howarth, Muriel Holder-Espinasse, Philippe Klee, Roxane Van-Heurk, Laure Lemmens, Maria Teresa Carminho-Rodrigues, Zainaba Mohamed, Aruna Goturu, Claire R. Hughes, Michal Ajzensztejn, N. Simon Thomas

Subjects: “…SHOX…”
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Clinical Evidence of Crossover in the SHOX Gene by Emine Göktaş, Mahmut Selman Yıldırım

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Large Deletions at the SHOX Locus in the Pseudoautosomal Region Are Associated with Skeletal Atavism in Shetland Ponies by Nima Rafati, Lisa S. Andersson, Sofia Mikko, Chungang Feng, Terje Raudsepp, Jessica Pettersson, Jan Janecka, Ove Wattle, Adam Ameur, Gunilla Thyreen, John Eberth, John Huddleston, Maika Malig, Ernest Bailey, Evan E. Eichler, Göran Dalin, Bhanu Chowdary, Leif Andersson, Gabriella Lindgren, Carl-Johan Rubin

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SHOX2 gene methylation in Egyptians having lung cancer by Mohamed Mostafa Mohamed Ahmed Rizk, Suzan Mohamed Farouk Helal, Ahmed Youssef Shaaban Gad, Doreen Nazeih Assaad Younan, Salma Abd El Maguid Mohamed Ramadan Moemen

Subjects: “…SHOX2…”
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Turner syndrome presented with tall stature due to overdosage of the gene by Go Hun Seo, Eungu Kang, Ja Hyang Cho, Beom Hee Lee, Jin-Ho Choi, Gu-Hwan Kim, Eul-Ju Seo, Han-Wook Yoo

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Co-occurrence of genomic imbalances on Xp22.1 in the SHOX region and 15q25.2 in a girl with short stature, precocious puberty, urogenital malformations and bone anomalies by Alice Monzani, Deepak Babu, Simona Mellone, Giulia Genoni, Antonella Fanelli, Flavia Prodam, Simonetta Bellone, Mara Giordano

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ANALYSIS OF GENE METHYLATION SHOX2, TGFBR1, MIR-375 IN DIFFERENT TYPES OF LUNG CANCER by D S Khodyrev, N S Kulagina, O I Brovkina, V E Pokrovsky, M G Gordiev, A S Кelekhsaeva, A G Nikitin, A V Averyanov

Subjects: “…shox2…”
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Copy number variations residing outside the SHOX enhancer region are involved in Short Stature and Léri‐Weill dyschondrosteosis by Antonella Fanelli, Silvia Vannelli, Deepak Babu, Simona Mellone, Alessia Cucci, Alice Monzani, Wael Al Essa, Andrea Secco, Antonia Follenzi, Simonetta Bellone, Flavia Prodam, Mara Giordano

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SHOX deficiency in children with growth impairment: evaluation of known and new auxological and radiological indicators by Silvia Vannelli, Maria Baffico, Raffaele Buganza, Francesca Verna, Giulia Vinci, Daniele Tessaris, Gianpaolo Di Rosa, Alberto Borraccino, Luisa de Sanctis

Subjects: “…SHOX…”
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Wrist radiography for hand bone age tells a lot; a girl with SHOX deficiency by Hüsnü Maraşlı, Nurullah Çelik, Yeşim Sidar Duman

Subjects: “…shox deficiency…”
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A potential immunotherapeutic and prognostic biomarker for multiple tumors including glioma: SHOX2 by Xiaocong Wu, Hui Chen, Chao You, Zongjun Peng

Subjects: “…SHOX2…”
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Knee X-Ray in Short Stature: Helpful Indicator to Diagnose SHOX Deficiency by Partha Pratim Chakraborty, Rana Bhattacharjee, Subhankar Chowdhury

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<i>SHOX</i> Deletion and Idiopathic Short Stature: What Does the Clinician Need to Know? Case Series Report by Maria-Christina Ungureanu, Anamaria Hrisca, Lavinia Caba, Laura Teodoriu, Stefana Bilha, Cristina Preda, Letitia Leustean

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Phenotypic characterization of patients with deletions in the 3’-flanking SHOX region by Sarina G. Kant, Sander J. Broekman, Caroline C. de Wit, Marloes Bos, Sitha A. Scheltinga, Egbert Bakker, Wilma Oostdijk, Hetty J. van der Kamp, Erik W. van Zwet, Annemieke H. van der Hout, Jan M. Wit, Monique Losekoot

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GH successful treatment in a female with a de novo 46,XX,add(X)(p36),t(X;Y)(p36.3;p11.2), growth impairment and SHOX-haploinsufficiency by Maria Cristina Maggio, Giovanni Corsello

Subjects: “…SHOX haploinsufficiency…”
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SHOX2 refines the identification of human sinoatrial nodal cell population in the in vitro cardiac differentiation by Takayuki Wakimizu, Kumi Morikawa, Kenta Fukumura, Tetsuo Yuki, Takashi Adachi, Yasutaka Kurata, Junichiro Miake, Ichiro Hisatome, Motokazu Tsuneto, Yasuaki Shirayoshi

Subjects: “…SHOX2…”
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Diagnostic value of SHOX2, RASSF1A gene methylation combined with CEA level detection in malignant pleural effusion by Shaosen Chen, Kunlun Huang, Lin Zou, Lu Chen, Peicun Hu

Subjects: “…SHOX2…”
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Screening of gene sequence variants in Saudi Arabian children with idiopathic short stature by Abdulla A. Alharthi, Ehab I. El-Hallous, Iman M. Talaat, Hamed A. Alghamdi, Matar I. Almalki, Ahmed Gaber

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Targeting G-quadruplex for rescuing impaired chondrogenesis in WRN-deficient stem cells by Adrian On-Wah Leung, Tsz-Ching Yiu, Lingxiao Liu, Hei-Yin Tam, Shen Gu, Jiajie Tu, Duanqing Pei, Hoi-Hung Cheung

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