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Items: 1 to 20 of 97

1.

PHF2, a novel PHD finger gene located on human chromosome 9q22.

Hasenpusch-Theil K, Chadwick BP, Theil T, Heath SK, Wilkinson DG, Frischauf AM.

Mamm Genome. 1999 Mar;10(3):294-8.

PMID:
10051327
2.

Molecular characterization of NSD1, a human homologue of the mouse Nsd1 gene.

Kurotaki N, Harada N, Yoshiura K, Sugano S, Niikawa N, Matsumoto N.

Gene. 2001 Nov 28;279(2):197-204.

PMID:
11733144
3.

Molecular cloning and functional characterization of murine transmembrane activator and CAML interactor (TACI) with chromosomal localization in human and mouse.

von B├╝low GU, Russell H, Copeland NG, Gilbert DJ, Jenkins NA, Bram RJ.

Mamm Genome. 2000 Aug;11(8):628-32.

PMID:
10920230
5.

Molecular cloning and characterization of the mouse and human TUSP gene, a novel member of the tubby superfamily.

Li QZ, Wang CY, Shi JD, Ruan QG, Eckenrode S, Davoodi-Semiromi A, Kukar T, Gu Y, Lian W, Wu D, She JX.

Gene. 2001 Aug 8;273(2):275-84.

PMID:
11595174
6.

cDNA isolation, genomic structure, regulation, and chromosomal localization of human lung Kruppel-like factor.

Wani MA, Conkright MD, Jeffries S, Hughes MJ, Lingrel JB.

Genomics. 1999 Aug 15;60(1):78-86.

PMID:
10458913
7.

Isolation, genomic organization, and expression analysis of Men1, the murine homolog of the MEN1 gene.

Guru SC, Crabtree JS, Brown KD, Dunn KJ, Manickam P, Prasad NB, Wangsa D, Burns AL, Spiegel AM, Marx SJ, Pavan WJ, Collins FS, Chandrasekharappa SC.

Mamm Genome. 1999 Jun;10(6):592-6.

PMID:
10341092
8.

Isolation and characterization of a human gene containing a nuclear localization signal from the critical region for velo-cardio-facial syndrome on 22q11.

Funke B, Puech A, Saint-Jore B, Pandita R, Skoultchi A, Morrow B.

Genomics. 1998 Oct 15;53(2):146-54.

PMID:
9790763
9.
10.

Cloning and analysis of the mouse Fanconi anemia group A cDNA and an overlapping penta zinc finger cDNA.

Wong JC, Alon N, Norga K, Kruyt FA, Youssoufian H, Buchwald M.

Genomics. 2000 Aug 1;67(3):273-83.

PMID:
10936049
11.

Mapping and characterization of a novel cochlear gene in human and in mouse: a positional candidate gene for a deafness disorder, DFNA9.

Robertson NG, Skvorak AB, Yin Y, Weremowicz S, Johnson KR, Kovatch KA, Battey JF, Bieber FR, Morton CC.

Genomics. 1997 Dec 15;46(3):345-54.

PMID:
9441737
12.

Characterization and in silico mapping of a novel murine zinc finger transcription factor.

Wride MA, Mansergh FC, Somani JM, Winkfein RJ, Rancourt DE.

Gene. 2002 May 1;289(1-2):49-59.

PMID:
12036583
13.

The murine DSCR1-like (Down syndrome candidate region 1) gene family: conserved synteny with the human orthologous genes.

Strippoli P, Petrini M, Lenzi L, Carinci P, Zannotti M.

Gene. 2000 Oct 31;257(2):223-32.

PMID:
11080588
14.

Structure, upstream promoter region, and functional domains of a mouse and human Mix paired-like homeobox gene.

Sahr K, Dias DC, Sanchez R, Chen D, Chen SW, Gudas LJ, Baron MH.

Gene. 2002 May 29;291(1-2):135-47.

PMID:
12095687
15.
16.

FKHL15, a new human member of the forkhead gene family located on chromosome 9q22.

Chadwick BP, Obermayr F, Frischauf AM.

Genomics. 1997 May 1;41(3):390-6.

PMID:
9169137
17.

Identification and characterization of the mouse MutS homolog 5: Msh5.

Her C, Wu X, Wan W, Doggett NA.

Mamm Genome. 1999 Nov;10(11):1054-61.

PMID:
10556423
18.

Cloning, mapping, and expression of two novel actin genes, actin-like-7A (ACTL7A) and actin-like-7B (ACTL7B), from the familial dysautonomia candidate region on 9q31.

Chadwick BP, Mull J, Helbling LA, Gill S, Leyne M, Robbins CM, Pinkett HW, Makalowska I, Maayan C, Blumenfeld A, Axelrod FB, Brownstein M, Gusella JF, Slaugenhaupt SA.

Genomics. 1999 Jun 15;58(3):302-9.

PMID:
10373328
19.
20.

EHD1--an EH-domain-containing protein with a specific expression pattern.

Mintz L, Galperin E, Pasmanik-Chor M, Tulzinsky S, Bromberg Y, Kozak CA, Joyner A, Fein A, Horowitz M.

Genomics. 1999 Jul 1;59(1):66-76.

PMID:
10395801
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