Lifton RP - Search Results

1

PPIL4 is essential for brain angiogenesis and implicated in intracranial aneurysms in humans.

Barak T, Ristori E, Ercan-Sencicek AG, Miyagishima DF, Nelson-Williams C, Dong W, Jin SC, Prendergast A, Armero W, Henegariu O, Erson-Omay EZ, Harmancı AS, Guy M, Gültekin B, Kilic D, Rai DK, Goc N, Aguilera SM, Gülez B, Altinok S, Ozcan K, Yarman Y, Coskun S, Sempou E, Deniz E, Hintzen J, Cox A, Fomchenko E, Jung SW, Ozturk AK, Louvi A, Bilgüvar K, Connolly ES Jr, Khokha MK, Kahle KT, Yasuno K, Lifton RP, Mishra-Gorur K, Nicoli S, Günel M. Barak T, et al. Among authors: lifton rp. Nat Med. 2021 Dec;27(12):2165-2175. doi: 10.1038/s41591-021-01572-7. Epub 2021 Dec 9. Nat Med. 2021. PMID: 34887573 Free PMC article.

2

Mapping a gene causing cerebral cavernous malformation to 7q11.2-q21.

Günel M, Awad IA, Anson J, Lifton RP. Günel M, et al. Among authors: lifton rp. Proc Natl Acad Sci U S A. 1995 Jul 3;92(14):6620-4. doi: 10.1073/pnas.92.14.6620. Proc Natl Acad Sci U S A. 1995. PMID: 7604043 Free PMC article.

3

A founder mutation as a cause of cerebral cavernous malformation in Hispanic Americans.

Gunel M, Awad IA, Finberg K, Anson JA, Steinberg GK, Batjer HH, Kopitnik TA, Morrison L, Giannotta SL, Nelson-Williams C, Lifton RP. Gunel M, et al. Among authors: lifton rp. N Engl J Med. 1996 Apr 11;334(15):946-51. doi: 10.1056/NEJM199604113341503. N Engl J Med. 1996. PMID: 8596595 Free article.

4

Counting strokes.

Günel M, Lifton RP. Günel M, et al. Among authors: lifton rp. Nat Genet. 1996 Aug;13(4):384-5. doi: 10.1038/ng0896-384. Nat Genet. 1996. PMID: 8696326 No abstract available.

5

Genetic heterogeneity of inherited cerebral cavernous malformation.

Günel M, Awad IA, Finberg K, Steinberg GK, Craig HD, Cepeda O, Nelson-Williams C, Lifton RP. Günel M, et al. Among authors: lifton rp. Neurosurgery. 1996 Jun;38(6):1265-71. doi: 10.1097/00006123-199606000-00059. Neurosurgery. 1996. PMID: 8727164

6

IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22-23.

Gharavi AG, Yan Y, Scolari F, Schena FP, Frasca GM, Ghiggeri GM, Cooper K, Amoroso A, Viola BF, Battini G, Caridi G, Canova C, Farhi A, Subramanian V, Nelson-Williams C, Woodford S, Julian BA, Wyatt RJ, Lifton RP. Gharavi AG, et al. Among authors: lifton rp. Nat Genet. 2000 Nov;26(3):354-7. doi: 10.1038/81677. Nat Genet. 2000. PMID: 11062479

7

Mutations in the Na-Cl cotransporter reduce blood pressure in humans.

Cruz DN, Simon DB, Nelson-Williams C, Farhi A, Finberg K, Burleson L, Gill JR, Lifton RP. Cruz DN, et al. Among authors: lifton rp. Hypertension. 2001 Jun;37(6):1458-64. doi: 10.1161/01.hyp.37.6.1458. Hypertension. 2001. PMID: 11408395

8

KRIT1, a gene mutated in cerebral cavernous malformation, encodes a microtubule-associated protein.

Gunel M, Laurans MS, Shin D, DiLuna ML, Voorhees J, Choate K, Nelson-Williams C, Lifton RP. Gunel M, et al. Among authors: lifton rp. Proc Natl Acad Sci U S A. 2002 Aug 6;99(16):10677-82. doi: 10.1073/pnas.122354499. Epub 2002 Jul 24. Proc Natl Acad Sci U S A. 2002. PMID: 12140362 Free PMC article.

9

Molecular pathogenesis of inherited hypertension with hyperkalemia: the Na-Cl cotransporter is inhibited by wild-type but not mutant WNK4.

Wilson FH, Kahle KT, Sabath E, Lalioti MD, Rapson AK, Hoover RS, Hebert SC, Gamba G, Lifton RP. Wilson FH, et al. Among authors: lifton rp. Proc Natl Acad Sci U S A. 2003 Jan 21;100(2):680-4. doi: 10.1073/pnas.242735399. Epub 2003 Jan 6. Proc Natl Acad Sci U S A. 2003. PMID: 12515852 Free PMC article.

10

WNK1, a kinase mutated in inherited hypertension with hyperkalemia, localizes to diverse Cl- -transporting epithelia.

Choate KA, Kahle KT, Wilson FH, Nelson-Williams C, Lifton RP. Choate KA, et al. Among authors: lifton rp. Proc Natl Acad Sci U S A. 2003 Jan 21;100(2):663-8. doi: 10.1073/pnas.242728499. Epub 2003 Jan 8. Proc Natl Acad Sci U S A. 2003. PMID: 12522152 Free PMC article.

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