The PDS Gene, Pendred Syndrome and Non-Syndromic Deafness (DFNB4)

Advances in Oto-Rhino-Laryngology - Genetics in Otorhinolaryngology ◽

10.1159/000059088 ◽

2000 ◽

pp. 145-151 ◽

Cited By ~ 8

Author(s):

E.R. Wilcox ◽

L.A. Everett ◽

X.C. Li ◽

A.K. Lalwani ◽

E.D. Green

Keyword(s):

Pendred Syndrome ◽

I Gene

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468: Polymorphic CA Repeats in IGF-I Gene is a Common Genetic Modifier in the Etiology of Prostate Cancer and Benign Prostatic Hyperplasia

The Journal of Urology ◽

10.1016/s0022-5347(18)37730-9 ◽

2004 ◽

Vol 171 (4S) ◽

pp. 125-125

Author(s):

Lizhong Wang ◽

Kazunari Sato ◽

Norihiko Tsuchiya ◽

Chikara Ohyama ◽

Shigeru Satoh ◽

...

Keyword(s):

Prostate Cancer ◽

Benign Prostatic Hyperplasia ◽

Genetic Modifier ◽

Prostatic Hyperplasia ◽

Igf I ◽

I Gene

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Altered gene causes Pendred syndrome: Finding leads to better understanding of deafness

PsycEXTRA Dataset ◽

10.1037/e634332007-001 ◽

1997 ◽

Keyword(s):

Pendred Syndrome ◽

Altered Gene

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TNF-α and IFN-γ-mediated signal transduction pathways: Effects on IRF-1 and MHC class I gene expression in oligodendrocytes

Immunology Letters ◽

10.1016/s0165-2478(97)88732-9 ◽

1997 ◽

Vol 56 (1-3) ◽

pp. 465

Author(s):

C Agresti

Keyword(s):

Gene Expression ◽

Signal Transduction ◽

Mhc Class I ◽

Class I ◽

Signal Transduction Pathways ◽

Tnf Α ◽

Ifn Γ ◽

I Gene ◽

Mhc Class I Gene

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Review for "Unique, gender‐dependent serum microRNA profile in PLS3 gene‐related osteoporosis"

10.1002/jbmr.4097/v2/review1 ◽

2020 ◽

Author(s):

Joshua R Lewis

Keyword(s):

Serum Microrna ◽

Microrna Profile ◽

I Gene

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The role of polymorphisms in the IGF-I gene in aging and age-related diseases

Experimental and Clinical Endocrinology & Diabetes ◽

10.1055/s-2004-832867 ◽

2004 ◽

Vol 112 (08) ◽

Author(s):

JAMJL Janssen

Keyword(s):

Age Related ◽

Igf I ◽

I Gene

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Identification of a novel germline mutation of the MEN I – gene (r.400delu) in a 24 year old patient with multifocal pancreatic insulinomas, primary hyperparathyroidism and a microprolactinoma

Experimental and Clinical Endocrinology & Diabetes ◽

10.1055/s-2007-972368 ◽

2007 ◽

Vol 115 (S 1) ◽

Author(s):

C Fottner ◽

T Minnemann ◽

JJ Wenzel ◽

H Rossmann ◽

KJ Lackner ◽

...

Keyword(s):

Primary Hyperparathyroidism ◽

Germline Mutation ◽

Men I ◽

I Gene

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PCR-RFLP Analysis Of Insulin-Like Growth Factor-I Gene In Bali Cattle

Jurnal Ilmu Peternakan Dan Veteriner ◽

10.30862/jipv.v5i1.756 ◽

2018 ◽

Vol 5 (1) ◽

Author(s):

Muhamad Affan Mu’in

Keyword(s):

Growth Factor ◽

Rflp Analysis ◽

Insulin Like Growth Factor ◽

Factor I ◽

Pcr Rflp ◽

Growth Factor I ◽

Bali Cattle ◽

I Gene

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Faculty Opinions recommendation of Photosynthesis nuclear genes generally lack TATA-boxes: a tobacco photosystem I gene responds to light through an initiator.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.1007007.40605 ◽

2002 ◽

Author(s):

Steven Spiker

Keyword(s):

Photosystem I ◽

Nuclear Genes ◽

I Gene

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Faculty Opinions recommendation of Oxygen tension regulates mitochondrial DNA-encoded complex I gene expression.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.1030073.355422 ◽

2006 ◽

Author(s):

Heinz Osiewacz

Keyword(s):

Gene Expression ◽

Mitochondrial Dna ◽

Oxygen Tension ◽

Complex I ◽

I Gene

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Faculty Opinions recommendation of A homozygous mutation of voltage-gated sodium channel β(I) gene SCN1B in a patient with Dravet syndrome.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.717972534.793469670 ◽

2013 ◽

Author(s):

Jeffrey Noebels ◽

Tara Klassen

Keyword(s):

Sodium Channel ◽

Dravet Syndrome ◽

Homozygous Mutation ◽

Voltage Gated Sodium Channel ◽

Voltage Gated ◽

I Gene

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