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Refinado por: Base de dados/Biblioteca: Academic Search Premier (EB_SDU_P3) remover assunto: Male remover Biochemistry & Molecular Biology remover
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1
In situ cryo-electron tomography reveals the asymmetric architecture of mammalian sperm axonemes
In situ cryo-electron tomography reveals the asymmetric architecture of mammalian sperm axonemes
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In situ cryo-electron tomography reveals the asymmetric architecture of mammalian sperm axonemes

Chen, Zhen ; Greenan, Garrett A ; Shiozaki, Momoko ; Liu, Yanxin ; Skinner, Will M ; Zhao, Xiaowei ; Zhao, Shumei ; Yan, Rui ; Yu, Zhiheng ; Lishko, Polina V ; Agard, David A ; Vale, Ronald D

Nature structural & molecular biology, 2023-03, Vol.30 (3), p.360-369 [Periódico revisado por pares]

United States: Nature Publishing Group

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2
Conditional inactivation of Miwi2 reveals that MIWI2 is only essential for prospermatogonial development in mice
Conditional inactivation of Miwi2 reveals that MIWI2 is only essential for prospermatogonial development in mice
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Conditional inactivation of Miwi2 reveals that MIWI2 is only essential for prospermatogonial development in mice

Bao, J ; Zhang, Y ; Schuster, A S ; Ortogero, N ; Nilsson, E E ; Skinner, M K ; Yan, W

Cell death and differentiation, 2014-05, Vol.21 (5), p.783-796 [Periódico revisado por pares]

England: Nature Publishing Group

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3
Serial magnetic resonance imaging of experimental atherosclerosis detects lesion fine structure, progression and complications in vivo
Serial magnetic resonance imaging of experimental atherosclerosis detects lesion fine structure, progression and complications in vivo
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Serial magnetic resonance imaging of experimental atherosclerosis detects lesion fine structure, progression and complications in vivo

Skinner, Michael P ; Yuan, Chun ; Mitsumori, Lee ; Hayes, Cecil E ; Raines M.P.S, Elaine W ; Nelson, James A ; Ross, Russell

Nature medicine, 1995-01, Vol.1 (1), p.69-73 [Periódico revisado por pares]

United States

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4
A new amyloidogenic transthyretin variant (Vail 22Ala) found in a compound heterozygous patient
A new amyloidogenic transthyretin variant (Vail 22Ala) found in a compound heterozygous patient
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A new amyloidogenic transthyretin variant (Vail 22Ala) found in a compound heterozygous patient

Théberge, R. ; Connors, L. ; Share, J. ; Skinner, M. ; Falk, R. H. ; Costello, C. E.

Amyloid, 1999, Vol.6 (1), p.54-58 [Periódico revisado por pares]

England: Informa UK Ltd

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5
Quantitative serum free light chain assay in the diagnostic evaluation of AL amyloidosis
Quantitative serum free light chain assay in the diagnostic evaluation of AL amyloidosis
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Quantitative serum free light chain assay in the diagnostic evaluation of AL amyloidosis

Akar, Harun ; Seldin, David C. ; Magnani, Barbarajean ; O'Hara, Carl ; Berk, John L. ; Schoonmaker, Christopher ; Cabral, Howard ; Dember, Laura M. ; Sanchorawala, Vaishali ; Connors, Lawreen H. ; Falk, Rodney H. ; Skinner, Martha

Amyloid, 2005-12, Vol.12 (4), p.210-215 [Periódico revisado por pares]

England: Informa UK Ltd

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6
A rare transthyretin mutation (Asp18Glu) associated with cardiomyopathy
A rare transthyretin mutation (Asp18Glu) associated with cardiomyopathy
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A rare transthyretin mutation (Asp18Glu) associated with cardiomyopathy

Connors, Lawreen Heller ; Yamashita, Taro ; Yazaki, Masahide ; Skinner, Martha ; Benson, Merrill D

Amyloid, 2004-03, Vol.11 (1), p.61-66 [Periódico revisado por pares]

England: Informa UK Ltd

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7
Identification of a novel transthyretin Thr59Lys/Arg104His. A case of compound heterozygosity in a Chinese patient diagnosed with familial transthyretin amyloidosis
Identification of a novel transthyretin Thr59Lys/Arg104His. A case of compound heterozygosity in a Chinese patient diagnosed with familial transthyretin amyloidosis
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Identification of a novel transthyretin Thr59Lys/Arg104His. A case of compound heterozygosity in a Chinese patient diagnosed with familial transthyretin amyloidosis

Lim, Amareth ; Prokaeva, Tatiana ; Connors, Lawreen H. ; Falk, Rodney H. ; Skinner, Martha ; Costello1, Catherine E.

Amyloid, 2002-06, Vol.9 (2), p.134-140 [Periódico revisado por pares]

England: Informa UK Ltd

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8
A new transthyretin variant (Ser2 sn) associated with familial amyloidosis in a Portuguese patient
A new transthyretin variant (Ser2 sn) associated with familial amyloidosis in a Portuguese patient
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A new transthyretin variant (Ser2 sn) associated with familial amyloidosis in a Portuguese patient

Connors, Lawreen Heller ; The'berge, Roger ; Skare, James ; Costello, Catherine E. ; Falk, Rodney H. ; Skinner, Martha

Amyloid, 1999, Vol.6 (2), p.114-118 [Periódico revisado por pares]

England: Informa UK Ltd

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9
Kaposi's sarcoma-associated herpesvirus gene sequences are detectable at low copy number in primary amyloidosis
Kaposi's sarcoma-associated herpesvirus gene sequences are detectable at low copy number in primary amyloidosis
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Kaposi's sarcoma-associated herpesvirus gene sequences are detectable at low copy number in primary amyloidosis

Raje, Noopur ; Chauhan, Dharminder ; Teoh, Gerrard ; Treon, Steven P. ; Hideshima, Teru ; Davies, Faith E. ; Tai, Y.-T. ; Pinkus, Geraldine S. ; Pinkus, Jack L. ; Anderson, Kenneth C. ; Kica, Geraldina ; Zhang, Yana ; Wally, Jeremy ; Skinner, Martha ; Comenzo, Raymond L. ; Deng, Jiang-Hong ; Gao, Shou-Jiang ; Alsina, Melissa

Amyloid, 2000, Vol.7 (2), p.126-132 [Periódico revisado por pares]

England: Informa UK Ltd

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