Publications:

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Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem

Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS

Publication Date: 2022-11

Variant appearance in text: rs133945

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

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Genetic variations influence brain changes in patients with attention-deficit hyperactivity disorder.

Translational Psychiatry

Yadav, Santosh K SK; Bhat, Ajaz A AA; Hashem, Sheema S; Nisar, Sabah S; Kamal, Madeeha M; Syed, Najeeb N; Temanni, Mohamed-Ramzi MR; Gupta, Rakesh K RK; Kamran, Saddat S; Azeem, Muhammad Waqar MW; Srivastava, Amit K AK; Bagga, Puneet P; Chawla, Sanjeev S; Reddy, Ravinder R; Frenneaux, Michael P MP; Fakhro, Khalid K; Haris, Mohammad M

Publication Date: 2021-06-05

Variant appearance in text: rs133945

PubMed Link: 34091591

Variant Present in the following documents:

• Main text
• 41398_2021_Article_1473.pdf

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Highly diversified core promoters in the human genome and their effects on gene expression and disease predisposition.

Bmc Genomics

Gupta, Hemant H; Chandratre, Khyati K; Sinha, Siddharth S; Huang, Teng T; Wu, Xiaobing X; Cui, Jian J; Zhang, Michael Q MQ; Wang, San Ming SM

Publication Date: 2020-11-30

Variant appearance in text: rs133945

PubMed Link: 33256598

Variant Present in the following documents:

• 12864_2020_7222_MOESM2_ESM.xlsx, sheet 3
• 12864_2020_7222_MOESM2_ESM.xlsx, sheet 2

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Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology

Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P

Publication Date: 2018

Variant appearance in text: SYN3: -162-34G>A; rs133945

PubMed Link: 30319441

Variant Present in the following documents:

• Table_7.xlsx, sheet 1
• Table_6.xlsx, sheet 1

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The impact of synapsin III gene on the neurometabolite level alterations after single-dose methylphenidate in attention-deficit hyperactivity disorder patients.

Neuropsychiatric Disease And Treatment

Başay, Ömer Ö; Kabukcu Basay, Burge B; Alacam, Huseyin H; Ozturk, Onder O; Buber, Ahmet A; Gorucu Yilmaz, Senay S; Kıroğlu, Yılmaz Y; Erdal, Mehmet Emin ME; Herken, Hasan H

Publication Date: 2016

Variant appearance in text: rs133945

PubMed Link: 27274248

Variant Present in the following documents:

• Main text
• ndt-12-1141.pdf

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Synapsin III: role in neuronal plasticity and disease.

Seminars In Cell & Developmental Biology

Porton, Barbara B; Wetsel, William C WC; Kao, Hung-Teh HT

Publication Date: 2011-06

Variant appearance in text: rs133945

PubMed Link: 21827867

Variant Present in the following documents:

• Main text

View BVdb publication page

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