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Items: 14

1.

VarSight: prioritizing clinically reported variants with binary classification algorithms.

Holt JM, Wilk B, Birch CL, Brown DM, Gajapathy M, Moss AC, Sosonkina N, Wilk MA, Anderson JA, Harris JM, Kelly JM, Shaterferdosian F, Uno-Antonison AE, Weborg A; Undiagnosed Diseases Network, Worthey EA.

BMC Bioinformatics. 2019 Oct 15;20(1):496. doi: 10.1186/s12859-019-3026-8.

2.

Mortalin (GRP75/HSPA9) Promotes Survival and Proliferation of Thyroid Carcinoma Cells.

Starenki D, Sosonkina N, Hong SK, Lloyd RV, Park JI.

Int J Mol Sci. 2019 Apr 26;20(9). pii: E2069. doi: 10.3390/ijms20092069.

3.

A Novel Association between the 27-bp Deletion and 538G>A Mutation in the ABCC11 Gene.

Hori YS, Yamada A, Matsuda N, Ono Y, Starenki D, Sosonkina N, Yoshiura KI, Niikawa N, Ohta T.

Hum Biol. 2017 Oct;89(4):305-307.

PMID:
30047321
4.

Characterization of Coding/Noncoding Variants for SHROOM3 in Patients with CKD.

Prokop JW, Yeo NC, Ottmann C, Chhetri SB, Florus KL, Ross EJ, Sosonkina N, Link BA, Freedman BI, Coppola CJ, McDermott-Roe C, Leysen S, Milroy LG, Meijer FA, Geurts AM, Rauscher FJ 3rd, Ramaker R, Flister MJ, Jacob HJ, Mendenhall EM, Lazar J.

J Am Soc Nephrol. 2018 May;29(5):1525-1535. doi: 10.1681/ASN.2017080856. Epub 2018 Feb 23.

5.

Kinome sequencing reveals RET G691S polymorphism in human neuroendocrine lung cancer cell lines.

Sosonkina N, Hong SK, Starenki D, Park JI.

Genes Genomics. 2014 Dec;36(6):829-841.

6.

The Role of STAT3 in Thyroid Cancer.

Sosonkina N, Starenki D, Park JI.

Cancers (Basel). 2014 Mar 6;6(1):526-44. doi: 10.3390/cancers6010526.

7.

Down-regulation of ABCC11 protein (MRP8) in human breast cancer.

Sosonkina N, Nakashima M, Ohta T, Niikawa N, Starenki D.

Exp Oncol. 2011 Mar;33(1):42-6.

PMID:
21423094
8.

Microarray comparative genomic hybridization analysis of 59 patients with schizophrenia.

Mizuguchi T, Hashimoto R, Itokawa M, Sano A, Shimokawa O, Yoshimura Y, Harada N, Miyake N, Nishimura A, Saitsu H, Sosonkina N, Niikawa N, Kunugi H, Matsumoto N.

J Hum Genet. 2008;53(10):914-9. doi: 10.1007/s10038-008-0327-6. Epub 2008 Aug 7.

PMID:
18685808
9.

Microarray comparative genomic hybridization (CGH)-based prenatal diagnosis for chromosome abnormalities using cell-free fetal DNA in amniotic fluid.

Miura S, Miura K, Masuzaki H, Miyake N, Yoshiura K, Sosonkina N, Harada N, Shimokawa O, Nakayama D, Yoshimura S, Matsumoto N, Niikawa N, Ishimaru T.

J Hum Genet. 2006;51(5):412-7. Epub 2006 Apr 19.

PMID:
16622586
10.

A SNP in the ABCC11 gene is the determinant of human earwax type.

Yoshiura K, Kinoshita A, Ishida T, Ninokata A, Ishikawa T, Kaname T, Bannai M, Tokunaga K, Sonoda S, Komaki R, Ihara M, Saenko VA, Alipov GK, Sekine I, Komatsu K, Takahashi H, Nakashima M, Sosonkina N, Mapendano CK, Ghadami M, Nomura M, Liang DS, Miwa N, Kim DK, Garidkhuu A, Natsume N, Ohta T, Tomita H, Kaneko A, Kikuchi M, Russomando G, Hirayama K, Ishibashi M, Takahashi A, Saitou N, Murray JC, Saito S, Nakamura Y, Niikawa N.

Nat Genet. 2006 Mar;38(3):324-30. Epub 2006 Jan 29.

PMID:
16444273
11.

BAC array CGH reveals genomic aberrations in idiopathic mental retardation.

Miyake N, Shimokawa O, Harada N, Sosonkina N, Okubo A, Kawara H, Okamoto N, Kurosawa K, Kawame H, Iwakoshi M, Kosho T, Fukushima Y, Makita Y, Yokoyama Y, Yamagata T, Kato M, Hiraki Y, Nomura M, Yoshiura K, Kishino T, Ohta T, Mizuguchi T, Niikawa N, Matsumoto N.

Am J Med Genet A. 2006 Feb 1;140(3):205-11.

PMID:
16419101
12.

No detectable genomic aberrations by BAC array CGH in Kabuki make-up syndrome patients.

Miyake N, Shimokawa O, Harada N, Sosonkina N, Okubo A, Kawara H, Okamoto N, Ohashi H, Kurosawa K, Naritomi K, Kaname T, Nagai T, Shotelersuk V, Hou JW, Fukushima Y, Kondoh T, Matsumoto T, Shinoki T, Kato M, Tonoki H, Nomura M, Yoshiura K, Kishino T, Ohta T, Niikawa N, Matsumoto N.

Am J Med Genet A. 2006 Feb 1;140(3):291-3. No abstract available.

PMID:
16278908
13.

Molecular characterization of del(8)(p23.1p23.1) in a case of congenital diaphragmatic hernia.

Shimokawa O, Miyake N, Yoshimura T, Sosonkina N, Harada N, Mizuguchi T, Kondoh S, Kishino T, Ohta T, Remco V, Takashima T, Kinoshita A, Yoshiura K, Niikawa N, Matsumoto N.

Am J Med Genet A. 2005 Jul 1;136(1):49-51.

PMID:
15937941
14.

Unmasking 15q12 deletion using microarray-based comparative genomic hybridization in a mentally retarded boy with r(Y).

Kurosawa K, Harada N, Sosonkina N, Niikawa N, Matsumoto N, Saitoh S.

Am J Med Genet A. 2004 Oct 15;130A(3):322-4. No abstract available.

PMID:
15378544

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